2023/04/07 更新

写真a

サトウ チヒロ
佐藤 ちひろ
SATO, Chihiro
所属
糖鎖生命コア研究所 統合生命医科学糖鎖研究センター 分子生理・動態部門 教授
大学院生命農学研究科 教授
大学院担当
大学院生命農学研究科
職名
教授
連絡先
メールアドレス

学位 3

  1. 博士(理学) ( 1997年3月   東京大学 ) 

  2. 修士(理学) ( 1994年3月   東京大学 ) 

  3. 学士(理学) ( 1992年3月   東京大学 ) 

研究キーワード 13

  1. 糖鎖生物学, 酸性糖鎖, シアル酸,ポリシアル酸, 神経, 脳, 生殖細胞, ラフト,精神疾患, 統合失調症, 自閉症, 双極性障害

  2. bipolar disorder

  3. 糖鎖生物学

  4. 酸性糖鎖

  5. 自閉症

  6. 統合失調症

  7. 精神疾患

  8. 神経

  9. 生殖細胞

  10. ラフト

  11. ポリシアル酸

  12. シアル酸

研究分野 8

  1. ライフサイエンス / 機能生物化学  / 機能生物化学

  2. ライフサイエンス / 構造生物化学  / 構造生物化学

  3. ライフサイエンス / 応用生物化学

  4. ライフサイエンス / 機能生物化学

  5. ナノテク・材料 / 生物分子化学

  6. ライフサイエンス / 構造生物化学

  7. ライフサイエンス / 応用分子細胞生物学

  8. ライフサイエンス / 医化学

▼全件表示

現在の研究課題とSDGs 3

  1. ジ・オリゴ・ポリシアル酸の構造と機能

  2. 疾患関連糖鎖の構造と機能

  3. 疾患に関わる糖鎖プローブの開発と利用

経歴 12

  1. 名古屋大学   糖鎖生命コア研究所   教授

    2021年1月 - 現在

  2. 名古屋大学   統合生命医科学糖鎖研究センター   所長(センター長)

    2021年1月 - 現在

  3. 名古屋大学   大学院生命農学研究科 応用生命科学専攻 応用生命科学   教授

    2019年10月 - 現在

  4. 名古屋大学   生物機能開発利用研究センター   准教授

    2007年4月 - 2019年9月

  5. 名古屋大学   生物機能開発利用研究センター 基盤・育成部門   助教授

    2005年2月 - 2007年3月

  6. 名古屋大学   大学院生命農学研究科 応用生命科学専攻   助教

    2001年8月 - 2005年1月

  7. 名古屋大学生物分子応答研究センター 研究機関研究員

    2001年4月 - 2001年8月

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    国名:日本国

  8. 名古屋大学生物分子応答研究センター 研究機関研究員

    2001年4月 - 2001年8月

  9. 日本学術振興会 特別研究員

    1998年4月 - 2001年3月

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    国名:日本国

  10. 日本学術振興会 特別研究員

    1998年4月 - 2001年3月

  11. 日本学術振興会 特別研究員

    1996年4月 - 1998年3月

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    国名:日本国

  12. 日本学術振興会 特別研究員

    1996年4月 - 1998年3月

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学歴 5

  1. 東京大学   大学院理学系研究科   生物化学専攻

    1994年4月 - 1997年3月

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    国名: 日本国

  2. 東京大学   大学院理学系研究科   生物化学専攻 博士課程

    1994年4月 - 1997年3月

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    国名: 日本国

  3. 東京大学   大学院理学系研究科   生物化学専攻

    1992年4月 - 1994年3月

  4. 東京大学   大学院理学系研究科   生物化学専攻 修士課程

    1992年4月 - 1994年3月

  5. 東京大学   理学部   生物化学

    1988年4月 - 1992年

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    国名: 日本国

所属学協会 13

  1. 日本生化学会   評議員

    2021年1月 - 現在

  2. 日本糖質学会   評議員

    2005年4月 - 現在

  3. 日本生化学会   中部支部会幹事

    2012年9月 - 2014年8月

  4. 日本糖鎖科学コンソーシアム(JCGG)   評議員

    2018年4月 - 現在

  5. 日本農芸化学会

  6. 糖鎖科学名古屋拠点   事務局

    2003年4月 - 現在

  7. ASBMB

  8. 日本神経科学会

  9. ASBMB

  10. 糖鎖科学名古屋拠点

  11. 日本農芸化学会

  12. 日本糖質学会

  13. 日本生化学会

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委員歴 8

  1. 日本生化学会   評議員  

    2021年1月 - 現在   

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    団体区分:学協会

  2. 日本糖質学会   評議員  

    2005年4月 - 現在   

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    団体区分:学協会

  3. 日本糖鎖科学コンソーシアム (JCGG)   評議員  

    2018年4月 - 現在   

  4. 日本生化学誌   企画委員  

    2017年9月 - 現在   

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    団体区分:学協会

  5. 日本農芸化学会 化学と生物   編集員  

    2016年4月 - 2021年3月   

  6. 日本生化学会中部支部会   幹事  

    2012年9月 - 2014年8月   

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    団体区分:学協会

  7. 日本農芸化学会   代議員  

    2009年4月 - 2011年3月   

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    団体区分:学協会

  8. 糖鎖科学中部拠点   事務局  

    2003年4月 - 現在   

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    団体区分:その他

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受賞 7

  1. 日本糖質学会奨励賞

    2003年   日本糖質学会  

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    受賞国:日本国

  2. 第1回日本農芸化学女性研究者賞

    2017年3月   日本農芸化学会  

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    受賞区分:国内学会・会議・シンポジウム等の賞  受賞国:日本国

  3. 第3回日本糖質学会ポスター賞

    1999年  

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    受賞国:日本国

  4. 2009年BBB論文賞

    2010年3月  

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    受賞国:日本国

  5. 2009年BBB論文賞

    2010年3月   日本農芸化学会  

    佐藤 ちひろ

  6. 第6回日本糖質学会奨励賞

    2003年3月   日本糖質学会  

    佐藤 ちひろ

  7. 第3回日本糖質学会ポスター賞

    1999年3月   日本糖質学会  

    佐藤 ちひろ

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論文 366

  1. Identification and characterization of a deaminoneuraminic acid (Kdn)-specific aldolase from Sphingobacterium species

    Nakagawa Takahiro, Iwaki Yuya, Wu Di, Hane Masaya, Sato Chihiro, Kitajima Ken

    GLYCOBIOLOGY     2022年8月

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    掲載種別:研究論文(学術雑誌)  

    DOI: 10.1093/glycob/cwac053

    Web of Science

  2. A novel C-domain-dependent inhibition of the rainbow trout CMP-sialic acid synthetase activity by CMP-deaminoneuraminic acid.

    Wu D, Gilormini PA, Toda S, Biot C, Lion C, Guérardel Y, Sato C, Kitajima K

    Biochemical and biophysical research communications   617 巻 ( Pt 1 ) 頁: 16 - 21   2022年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical and Biophysical Research Communications  

    The CMP-sialic acid synthetase (CSS) activates free sialic acid (Sia) to CMP-Sia using CTP, and is prerequisite for the sialylation of cell surface glycoconjugates. The vertebrate CSS consists of two domains, a catalytic N-domain and a non-catalytic C-domain. Although the C-domain is not required for the CSS enzyme to synthesize CMP-Sia, its involvement in the catalytic activity remains unknown. First, the real-time monitoring of CSS-catalyzed reaction was performed by 31P NMR using the rainbow trout CSS (rtCSS). While a rtCSS lacking the C-domain (rtCSS-N) similarly activated both deaminoneuraminic acid (Kdn) and N-acetylneuraminic acid (Neu5Ac), the full-length rtCSS (rtCSS-FL) did not activate Kdn as efficiently as Neu5Ac. These results suggest that the C-domain of rtCSS affects the enzymatic activity, when Kdn was used as a substrate. Second, the enzymatic activity of rtCSS-FL and rtCSS-N was measured under various concentrations of CMP-Kdn. Inhibition by CMP-Kdn was observed only for rtCSS-FL, but not for rtCSS-N, suggesting that the inhibition was C-domain-dependent. Third, the inhibitory effect of CMP-Kdn was also investigated using the mouse CSS (mCSS). However, no inhibition was observed with mCSS even at high concentrations of CMP-Kdn. Taken together, the data demonstrated that the C-domain is involved in the CMP-Kdn-dependent inhibition of rtCSS, which is a novel regulation of the Sia metabolism in rainbow trout.

    DOI: 10.1016/j.bbrc.2022.05.031

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  3. Sulfation of sialic acid is ubiquitous and essential for vertebrate development.

    Ertunc N, Phitak T, Wu D, Fujita H, Hane M, Sato C, Kitajima K

    Scientific reports   12 巻 ( 1 ) 頁: 12496   2022年7月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Scientific Reports  

    Glycosylation of proteins and lipids occurs in vertebrates, usually terminating with sialylation, which regulates the physicochemical and biological properties of these glycoconjugates. Although less commonly known, sialic acid residues also undergo various modifications, such as acetylation, methylation, and sulfation. However, except for acetylation, the enzymes or functions of the other modification processes are unknown. To the best of our knowledge, this study is the first to demonstrate the ubiquitous occurrence of sulfated sialic acids and two genes encoding the sialate: O-sulfotransferases 1 and 2 in vertebrates. These two enzymes showed about 50% amino acid sequence identity, and appeared to be complementary to each other in acceptor substrate preferences. Gene targeting experiments showed that the deficiency of these genes was lethal for medaka fish during young fry development and accompanied by different phenotypes. Thus, the sulfation of sialic acids is essential for the vertebrate development.

    DOI: 10.1038/s41598-022-15143-4

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  4. Shrimp thrombospondin (TSP): presence of O-β1,4 N-acetylglucosamine polymers and its function in TSP chain association in egg extracellular matrix.

    Magerd S, Senarai T, Thongsum O, Chawiwithaya C, Sato C, Kitajima K, Weerachatyanukul W, Asuvapongpatana S, Surinlert P

    Scientific reports   12 巻 ( 1 ) 頁: 7925   2022年5月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Scientific Reports  

    We characterized the existence of O-β(1,4)-GlcNAc polymers (β1,4GNP) that were anchored on the O-linked glycosylation sites of shrimp thrombospondin (pmTSP-II). There were five putative β1,4GNP linkages on the epithelial growth factor-like domain of pmTSP-II. Antibody against O-β-GlcNAc (CTD110.6) was used to prove the existence of linear and complex β1,4GNP. The antibody well reacted with linear chito-triose, -tetraose and -pentaose conjugated with phosphatidylethanolamine lipid. The immunoreactivity could also be detected with a complex β1,4GNP within pmTSP-II (at MW > 250 kDa). Upon denaturing the protein with SDS-PAGE buffer, the size of pmTSP-II was shifted to be 250 kDa, approximately 2.5 folds larger than the deduced molecular mass of pmTSP-II (110 kDa), suggesting additional association of pmTSP-II apart from its known disulfide bridging. This was confirmed by chitinase digestion on pmTSP-II protein leading to the subsequent smaller protein bands at 110–170 kDa in time- and concentration-dependent manners. These bands well reacted with CTD110.6 antibody and disappeared after extensive chitinase hydrolysis. Together, we believe that β1,4GNP on pmTSP-II serve the function in an inter-chain association to provide structural architecture of egg extracellular matrix, a novel function of pmTSP-II in reproductive biology.

    DOI: 10.1038/s41598-022-11873-7

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  5. Analysis of biochemical features of ST8 α-N-acetyl-neuraminide α2,8-sialyltransferase (St8sia) 5 isoforms.

    Araki E, Hane M, Hatanaka R, Kimura R, Tsuda K, Konishi M, Komura N, Ando H, Kitajima K, Sato C

    Glycoconjugate journal   39 巻 ( 2 ) 頁: 291 - 302   2022年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycoconjugate Journal  

    Gangliosides are important components of the membrane and are involved in many biological activities. St8sia5 is an α2,8-sialyltransferase involved in ganglioside synthesis, and has three isoforms. In this study, we analyzed the features of three isoforms, St8sia5-S, -M, and -L that had not been analyzed, and found that only St8sia5-L was localized in the Golgi, while the majority of St8sia5-M and -S were localized in the ER. The localization of Golgi of St8sia5 depended on the stem region. In addition, the incorporation of exogenous GD3 was upregulated only in St8sia5-L expressing cells. Taken together, the localization of St8sia5 is important for the activity of the enzyme.

    DOI: 10.1007/s10719-021-10034-8

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  6. A point-mutation in the C-domain of CMP-sialic acid synthetase leads to lethality of medaka due to protein insolubility.

    Wu D, Arakawa H, Fujita A, Hashimoto H, Hibi M, Naruse K, Kamei Y, Sato C, Kitajima K

    Scientific reports   11 巻 ( 1 ) 頁: 23211   2021年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Scientific Reports  

    Vertebrate CMP-sialic acid synthetase (CSS), which catalyzes the synthesis of CMP-sialic acid (CMP-Sia), consists of a 28 kDa-N-domain and a 20 kDa-C-domain. The N-domain is known to be a catalytic domain; however, the significance of the C-domain still remains unknown. To elucidate the function of the C-domain at the organism level, we screened the medaka TILLING library and obtained medaka with non-synonymous mutations (t911a), or single amino acid substitutions of CSS, L304Q, in the C-domain. Prominently, most L304Q medaka was lethal within 19 days post-fertilization (dpf). L304Q young fry displayed free Sia accumulation, and impairment of sialylation, up to 8 dpf. At 8 dpf, a marked abnormality in ventricular contraction and skeletal myogenesis was observed. To gain insight into the mechanism of L304Q-induced abnormalities, L304Q was biochemically characterized. Although bacterially expressed soluble L304Q and WT showed the similar Vmax/Km values, very few soluble L304Q was detected when expressed in CHO cells in sharp contrast to the WT. Additionally, the thermostability of various mutations of L304 greatly decreased, except for WT and L304I. These results suggest that L304 is important for the stability of CSS, and that an appropriate level of expression of soluble CSS is significant for animal survival.

    DOI: 10.1038/s41598-021-01715-3

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  7. Identification and functional characterization of a Siglec-7 counter-receptor on K562 cells. 査読有り 国際共著

    Yoshimura A, Asahina Y, Chang LY, Angata T, Tanaka H, Kitajima K, Sato C

    The Journal of biological chemistry   296 巻   頁: 100477   2021年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    Sialic acid (Sia)-binding immunoglobulin-like lectin 7 (Siglec-7) is an inhibitory receptor primarily expressed on natural killer (NK) cells and monocytes. Siglec-7 is known to negatively regulate the innate immune system through Sia binding to distinguish self and nonself; however, a counterreceptor bearing its natural ligand remains largely unclear. Here, we identified a counter-receptor of Siglec-7 using K562 hematopoietic carcinoma cells presenting cell surface ligands for Siglec-7. We affinity-purified the ligands using Fc-ligated recombinant Siglec-7 and diSia-dextran polymer, a strong inhibitor for Siglec-7. We then confirmed the counter-receptor for Siglec-7 as leukosialin (CD43) through mass spectrometry, immunoprecipitation, and proximity labeling. Additionally, we demonstrated that the cytotoxicity of NK cells toward K562 cells was suppressed by overexpression of leukosialin in a Siglec-7-dependent manner. Taken together, our data suggest that leukosialin on K562 is a counter-receptor for Siglec-7 on NK cells and that a cluster of the Sia-containing glycan epitope on leukosialin is key as trans-ligand for unmasking the cis-ligand.

    DOI: 10.1016/j.jbc.2021.100477

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  8. Lower promoter activity of the ST8SIA2 gene has been favored in evolving human collective brains.

    Hayakawa T, Terahara M, Fujito NT, Matsunaga T, Teshima KM, Hane M, Kitajima K, Sato C, Takahata N, Satta Y

    PloS one   16 巻 ( 12 ) 頁: e0259897   2021年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:PLoS ONE  

    ST8SIA2 is an important molecule regulating expression of the phenotype involved in schizophrenia. Lowered promoter activity of the ST8SIA2 gene is considered to be protective against schizophrenia by conferring tolerance to psychosocial stress. Here, we examined the promoter-type composition of anatomically modern humans (AMHs) and archaic humans (AHs; Neanderthals and Denisovans), and compared the promoter activity at the population level (population promoter activity; PPA) between them. In AMHs, the TCT-type, showing the second lowest promoter activity, was most prevalent in the ancestral population of non-Africans. However, the detection of only the CGT-type from AH samples and recombination tracts in AH sequences showed that the CGT- and TGT-types, exhibiting the two highest promoter activities, were common in AH populations. Furthermore, interspecies gene flow occurred into AMHs from AHs and into Denisovans from Neanderthals, influencing promoter-type compositions independently in both AMHs and AHs. The difference of promoter-type composition makes PPA unique in each population. East and Southeast Asian populations show the lowest PPA. This results from the selective increase of the CGC-type, showing the lowest promoter activity, in these populations. Every non-African population shows significantly lower PPA than African populations, resulting from the TCT-type having the highest prevalence in the ancestral population of non-Africans. In addition, PPA reduction is also found among subpopulations within Africa via a slight increase of the TCT-type. These findings indicate a trend toward lower PPA in the spread of AMHs, interpreted as a continuous adaptation to psychosocial stress arising in migration. This trend is considered as genetic tuning for the evolution of collective brains. The inferred promoter-type composition of AHs differed markedly from that of AMHs, resulting in higher PPA in AHs than in AMHs. This suggests that the trend toward lower PPA is a unique feature in AMH spread.

    DOI: 10.1371/journal.pone.0259897

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  9. The expression of sulfated sialic acids (SiaS) is dynamically regulated in mammalian cells

    Kitajima Ken, Ertunc Nursah, Sato Chihiro

    GLYCOBIOLOGY   30 巻 ( 12 ) 頁: 1066 - 1067   2020年12月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  10. Sialic acid sulfation is induced by the antibiotic treatment in mammalian cells.

    Ertunc N, Sato C, Kitajima K

    Bioscience, biotechnology, and biochemistry   84 巻 ( 11 ) 頁: 2311 - 2318   2020年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Bioscience, Biotechnology and Biochemistry  

    Sialic acids (Sias) are an outermost-situated sugar of glycoproteins and glycolipids to play important roles in various biological phenomena. They are often modified by additional substituents, such as O-acetyl group, to display more than 50 different structures in nature. Of those modified Sia, nothing is known about the occurrence and biological functions of sulfated Sias (SiaSs) in mammals. To elucidate the significance of sialic acid sulfation, we investigated various mammalian-cultured cell lines for the expression of SiaS using the specific antibody 3G9. First, SiaS is expressed in a cell line-dependent and a cell density-dependent manner. Second, in CHO cells, the expression of SiaS is reversibly induced by treatment with the antibiotic G418. Taken together, the expression of SiaS is changed by intrinsic and extrinsic factors in mammalian cells. This is the first demonstration of regulated expression of SiaS.

    DOI: 10.1080/09168451.2020.1792763

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    CiNii Research

  11. ゼブラフィッシュの全組織グライコミクス

    北島 健, 山川 奈緒, 佐藤 ちひろ, ヤン ゲラルデル

    生化学   92 巻 ( 3 ) 頁: 349 - 359   2020年6月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:公益社団法人日本生化学会  

    ゼブラフィッシュの成体臓器について全グライコーム解析を行い,タンパク質N-グリカンおよびO-グリカン,糖脂質(GSLs)について,それぞれ249, 69, 286種類が同定され,豊富で多種多様なグライコームが証明された.数多くの哺乳類と共通な構造に加え,そこに特徴的な糖残基付加が起こって形成されるゼブラフィッシュ特異的構造も存在する一方,ゼブラフィッシュには存在しない哺乳類特有な構造の存在も明らかになった.また,全グライコーム解析から腸における細菌叢に由来する単糖が臓器内の代謝に利用される実態がわかり,新しい生理学的過程の発見となった.本研究のゼブラフィッシュの臓器特異的グライコーム地図が,特異的な糖鎖関連酵素遺伝子の発現パターンと合わせて提供されれば,ゼブラフィッシュの糖鎖機能解析における有効利用が期待される.

    DOI: 10.14952/seikagaku.2020.920349

    CiNii Research

  12. Identification and characterization of a novel, versatile sialidase from a Sphingobacterium that can hydrolyze the glycosides of any sialic acid species at neutral pH. 査読有り

    Iwaki Y, Matsunaga E, Takegawa K, Sato C, Kitajima K

    Biochemical and biophysical research communications   523 巻 ( 2 ) 頁: 487 - 492   2020年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical and Biophysical Research Communications  

    Bacterial sialidases are widely used to remove sialic acid (Sia) residues from glycans. Most of them cleave the glycosides of N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5Gc) under acidic pHs; however, currently available bacterial sialidases had no activity to the glycosides of deaminoneuraminic acid (Kdn). In this study, we found a novel sialidase from Sphingobacterium sp. strain HMA12 that could cleave any of the glycosides of Neu5Ac, Neu5Gc, and Kdn. It also had a broad linkage specificity, i.e., α2,3-, α2,6-, α2,8-, and α2,9-linkages, and the optimal pH at neutral ranges, pH 6.5–7.0. These properties are particularly important when sialidases are applied for in vivo digestion of the cell surface sialosides under physiological conditions. Interestingly, 2,3-didehydro-2-deoxy-N-acetylneuraminic acid (Neu5Ac2en), which is a transition state analog-based inhibitor, competitively inhibited the enzyme-catalyzed reaction for Kdn as well as for Neu5Ac, suggesting that the active site is common to the Neu5Ac and Kdn residues. Taken together, this sialidase is versatile and useful for the in vivo research on sialo-glycoconjugates.

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  13. PSA-NCAM Colocalized with Cholecystokinin-Expressing Cells in the Hippocampus Is Involved in Mediating Antidepressant Efficacy. 査読有り

    Yamada J, Sato C, Konno K, Watanabe M, Jinno S

    The Journal of neuroscience : the official journal of the Society for Neuroscience   40 巻 ( 4 ) 頁: 825 - 842   2020年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Neuroscience  

    The extracellular glycan polysialic acid linked to neural cell adhesion molecule (PSA-NCAM) is principally expressed in the developing brain and the adult neurogenic regions. Although colocalization of PSA-NCAM with cholecystokinin (CCK) was found in the adult brain, the role of PSA-NCAM remains unclear. In this study, we aimed to elucidate the functional significance of PSA-NCAM in the CA1 region of the male mouse hippocampus. Combined fluorescence in situ hybridization and immunohistochemistry showed that few vesicular glutamate transporter 3-negative/CCK-positive (VGluT3 –/CCK +) cells were colocalized with PSA-NCAM, but most of the VGluT3 +/ CCK + cells were colocalized with PSA-NCAM. The somata of PSA-NCAM +/CCK + cells were highly innervated by serotonergic boutons than those of PSA-NCAM –/CCK + cells. The expression ratios of 5-HT3A receptors and p11, a serotonin receptor-interacting protein, were higher in PSA-NCAM +/CCK + cells than in PSA-NCAM –/CCK + cells. Pharmacological digestion of PSA-NCAM impaired the efficacy of antidepressant fluoxetine (FLX), a selective serotonin reuptake inhibitor, but not the efficacy of benzodiazepine anxiolytic diazepam. A Western blot showed that restraint stress decreased the expressions of p11 and mature brain-derived neurotrophic factor (BDNF), and FLX increased them. Interestingly, the FLX-induced elevation of expression of p11, but not mature BDNF, was impaired by the digestion of PSA-NCAM. Quantitative reverse transcription-polymerase chain reaction showed that restraint stress reduced the expression of polysialyltransferase ST8Sia IV and FLX elevated it. Collectively, PSA-NCAM colocalized with VGluT3 +/CCK + cells in the CA1 region of the hippocampus may play a unique role in the regulation of antidepressant efficacy via the serotonergic pathway.

    DOI: 10.1523/JNEUROSCI.1779-19.2019

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  14. ジ・オリゴ・ポリシアル酸(シアル酸重合体)の構造と機能解析 招待有り

    佐藤 ちひろ

    Trends in Glycoscience and Glycotechnology   31 巻 ( 181 ) 頁: SJ32 - SJ35   2019年7月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:FCCA(Forum: Carbohydrates Coming of Age)  

    <p>シアル酸は糖鎖の非還元末端に一分子存在するモノシアリル基での存在がよく知られている。しかしながら天然にはシアル酸がシアル酸同士で結合したジ・オリゴ・ポリシアル酸構造での存在が知られている。私はこれまでシアル酸重合体に対して、その検出方法を開発して以来、シアル酸重合体の構造と機能の解析を一貫して行ってきた。その結果これまでにその重合度のもつ生物学的な意義の一端を明らかにしてきた。特にポリシアル酸に関してはこれまでのポリシアル酸の機能の概念を覆すことに繋がった。また一連の研究は近年精神疾患や癌研究へと繋がっている。</p>

    DOI: 10.4052/tigg.1915.2sj

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  15. Structure and Function of di/oligo/polysialic Acid (Polymerized Sialyl Structure) 招待有り

    Sato Chihiro

    TRENDS IN GLYCOSCIENCE AND GLYCOTECHNOLOGY   31 巻 ( 181 ) 頁: SE32 - SE35   2019年7月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Trends in Glycoscience and Glycotechnology  

    Sialic acid (Sia) is known to present as a monosialyl residue at a non-reducing terminal end of glycan in nature. In some cases, Sias occur as polymerized sialyl structures, di/oligo/polysialic acids (diSia/oligoSia/polySias). Here, we focus on the structure, function and biological significance of diSia/oligoSia/polySias. Following the definition of di/oligo/polySia structures and establishment of chemical and immunochemical detection methods, we analyzed these structures and their function based on a set of working hypotheses. So far, the biological meanings of degree of polymerization (DP) were shown and they lead to the change the concept of polySia. In addition, this research is applicable in the study of diseases such as mental disorder and cancer. However, research on the biological significance of the diversity in di/oligo/polySia structures is still ongoing.

    DOI: 10.4052/tigg.1915.2SE

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  16. Glycans in Nervous System 査読有り

    Sato Chihiro, Gu Jianguo, Fukuda Tomohiko, Kadomatsu Kenji, Ikenaka Kazuhiro

    GLYCOSCIENCE: BASIC SCIENCE TO APPLICATIONS: INSIGHTS FROM THE JAPAN CONSORTIUM FOR GLYCOBIOLOGY AND GLYCOTECHNOLOGY (JCGG)     頁: 209 - 219   2019年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycoscience: Basic Science to Applications: Insights from the Japan Consortium for Glycobiology and Glycotechnology (JCGG)  

    DOI: 10.1007/978-981-13-5856-2_12

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  17. 酸性糖鎖ポリシアル酸の新機能の発見とその応用展開

    佐藤 ちひろ

    化学と生物   56 巻 ( 6 ) 頁: 422 - 431   2018年5月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:公益社団法人 日本農芸化学会  

    <p>ポリシアル酸は酸性9炭糖のシアル酸の直鎖状ホモポリマーの総称であり,神経細胞接着分子(NCAM)を時・空間特異的に修飾するがん胎児性抗原として知られている.ポリシアル酸が生み出す排他的空間が細胞–細胞/細胞外マトリックスの接着を抑制することで,脳機能のさまざまな調節を行っていると久しく考えられてきた.近年,ポリシアル酸がこの反接着性の機能だけではなく,生理活性分子を構造特異的に保持する機能をもつことが明らかにされ,親和的な空間を作り出すことにより,さまざまな因子群の機能制御を行っていることが示された.さらに,この構造を作り出す生合成酵素と統合失調症をはじめとする精神疾患との関連性が注目されている.ここでは,近年明らかになってきたポリシアル酸の新しい機能を中心に解説する.</p>

    DOI: 10.1271/kagakutoseibutsu.56.422

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  18. Polysialyltransferase ST8SIA2 and psychiatric disorders

    Hane M., Kitajima K., Sato C.

    Seikagaku   89 巻 ( 5 ) 頁: 634 - 643   2017年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Seikagaku  

    DOI: 10.14952/SEIKAGAKU.2017.890634

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  19. ポリシアル酸転移酵素遺伝子ST8SIA2と精神疾患の関わり 査読有り

    羽根 正弥, 佐藤 ちひろ

    生化学   89 巻   頁: 634 - 643   2017年

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    掲載種別:研究論文(学術雑誌)  

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  20. Hsp70の酸性複合糖質結合活性の発見. 糖の意外な働き. 査読有り

    佐藤 ちひろ

    化学と生物   55, 巻   頁: 22 - 26   2017年

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    掲載種別:研究論文(学術雑誌)  

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  21. The Out of Africa and mental disorders: Adaptation with reduction in STX promoter activity

    Fujito Naoko, Satta Yoko, Hane Masaya, Matsui Atsushi, Yashima Kenta, Kitajima Ken, Sato Chihiro, Takahata Naoyuki, Hayakawa Toshiyuki

    GENES & GENETIC SYSTEMS   91 巻 ( 6 ) 頁: 343 - 343   2016年12月

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    掲載種別:研究論文(学術雑誌)  

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  22. A Uniquely Human Evolutionary Change in ST8Sia-II Impacts Enzyme Stability and Polysialic Acid Function

    Vaill Michael, Hane Masaya, Naito-Matsui Yuko, Diaz Sandra, Davies Leela, Kitajima Ken, Sato Chihiro, Varki Ajit

    GLYCOBIOLOGY   26 巻 ( 12 ) 頁: 1423 - 1423   2016年12月

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    掲載種別:研究論文(学術雑誌)  

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  23. Hsp70の酸性複合糖質結合活性の発見

    原田 陽一郎, 佐藤 ちひろ, 北島 健

    化学と生物   55 巻 ( 1 ) 頁: 22 - 26   2016年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:公益社団法人 日本農芸化学会  

    DOI: 10.1271/kagakutoseibutsu.55.22

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  24. Spread of reduced activity of STX promoter throughout Great Journey

    Fujito Naoko, Satta Yoko, Hane Masaya, Matsui Atsushi, Kitajima Ken, Sato Chihiro, Hayakawa Toshiyuki

    GENES & GENETIC SYSTEMS   90 巻 ( 6 ) 頁: 379 - 379   2015年12月

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    掲載種別:研究論文(学術雑誌)  

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  25. Protective effects of polysialic acid on proteolytic cleavage of FGF2 and proBDNF/BDNF.

    Hane M, Matsuoka S, Ono S, Miyata S, Kitajima K, Sato C

    Glycobiology   25 巻 ( 10 ) 頁: 1112 - 24   2015年10月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    Polysialic acid (polySia) is a linear polymer of sialic acid that modifies neural cell adhesion molecule (NCAM) in the vertebrate brain. PolySia is a large and exclusive molecule that functions as a negative regulator of cell-cell interactions. Recently, we demonstrated that polySia can specifically bind fibroblast growth factor 2 (FGF2) and BDNF; however, the protective effects of polySia on the proteolytic cleavage of these proteins remain unknown, although heparin/heparan sulfate has been shown to impair the cleavage of FGF2 by trypsin. Here, we analyzed the protective effects of polySia on the proteolytic cleavage of FGF2 and proBDNF/BDNF. We found that polySia protected intact FGF2 from tryptic activity via the specific binding of extended polySia chains on NCAM to FGF2. Oligo/polySia also functioned to impair the processing of proBDNF by plasmin via binding of oligo/polySia chains on NCAM. In addition, the polySia structure synthesized by mutated polysialyltransferase, ST8SIA2/STX(SNP7), which was previously identified from a schizophrenia patient, was impaired for these functions compared with polySia produced by normal ST8SIA2. Taken together, these data suggest that the protective effects of polySia toward FGF2 and proBDNF may be involved in the regulation of the concentrations of these neurologically active molecules.

    DOI: 10.1093/glycob/cwv049

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  26. Ganglioside contained in the neuronal tissue-enriched acidic protein of 22 kDa (NAP-22) fraction prepared from the detergent-resistant membrane microdomain of rat brain inhibits the phosphatase activity of calcineurin.

    Kobayashi Y, da Silva R, Kumanogoh H, Miyata S, Sato C, Kitajima K, Nakamura S, Morita M, Hayashi F, Maekawa S

    Journal of neuroscience research   93 巻 ( 9 ) 頁: 1462 - 70   2015年9月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Neuroscience Research  

    Neurons have well-developed membrane microdomains called "rafts" that are recovered as a detergent-resistant membrane microdomain fraction (DRM). Neuronal tissue-enriched acidic protein of 22 kDa (NAP-22) is one of the major protein components of neuronal DRM. To determine the cellular function of NAP-22, interacting proteins were screened with an immunoprecipitation assay, and calcineurin (CaN) was detected. Further studies with NAP-22 prepared from DRM and CaN expressed in bacteria showed the binding of these proteins and a dose-dependent inhibitory effect of the NAP-22 fraction on the phosphatase activity of CaN. On the other hand, NAP-22 expressed in bacteria showed low binding to CaN and a weak inhibitory effect on phosphatase activity. To solve this discrepancy, identification of a nonprotein component that modulates CaN activity in the DRM-derived NAP-22 fraction was attempted. After lyophilization, a lipid fraction was extracted with chloroform/methanol. The lipid fraction showed an inhibitory effect on CaN without NAP-22, and further fractionation of the extract with thin-layer chromatography showed the presence of several lipid bands having an inhibitory effect on CaN. The mobility of these bands coincided with that of authentic ganglioside (GM1a, GD1a, GD1b, and GT1b), and authentic ganglioside showed an inhibitory effect on CaN. Treatment of lipid with endoglycoceramidase, which degrades ganglioside to glycochain and ceramide, caused a diminution of the inhibitory effect. These results show that DRM-derived NAP-22 binds several lipids, including ganglioside, and that ganglioside inhibits the phosphatase activity of CaN.

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  27. Rapid Trimming of Cell Surface Polysialic Acid (PolySia) by Exovesicular Sialidase Triggers Release of Preexisting Surface Neurotrophin.

    Sumida M, Hane M, Yabe U, Shimoda Y, Pearce OM, Kiso M, Miyagi T, Sawada M, Varki A, Kitajima K, Sato C

    The Journal of biological chemistry   290 巻 ( 21 ) 頁: 13202 - 14   2015年5月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    As acidic glycocalyx on primary mouse microglial cells and a mouse microglial cell line Ra2, expression of polysialic acid (polySia/PSA), a polymer of the sialic acid Neu5Ac (N-acetylneuraminic acid), was demonstrated. PolySia is known to modulate cell adhesion, migration, and localization of neurotrophins mainly on neural cells. PolySia on Ra2 cells disappeared very rapidly after an inflammatory stimulus. Results of knockdown and inhibitor studies indicated that rapid surface clearance of polySia was achieved by secretion of endogenous sialidase Neu1 as an exovesicular component. Neu1-mediated polySia turnover was accompanied by the release of brain-derived neurotrophic factor normally retained by polySia molecules. Introduction of a single oxygen atom change into polySia by exogenous feeding of the non-neural sialic acid Neu5Gc (N-glycolylneuraminic acid) caused resistance to Neu1-induced polySia turnover and also inhibited the associated release of brain-derived neurotrophic factor. These results indicate the importance of rapid turnover of the poly-Sia glycocalyx by exovesicular sialidases in neurotrophin regulation.

    DOI: 10.1074/jbc.M115.638759

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  28. Sulfatide-Hsp70 interaction promotes Hsp70 clustering and stabilizes binding to unfolded protein.

    Harada Y, Sato C, Kitajima K

    Biomolecules   5 巻 ( 2 ) 頁: 958 - 73   2015年5月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biomolecules  

    The 70-kDa heat shock protein (Hsp70), one of the major stress-inducible molecular chaperones, is localized not only in the cytosol, but also in extracellular milieu in mammals. Hsp70 interacts with various cell surface glycolipids including sulfatide (3'-sulfogalactosphingolipid). However, the molecular mechanism, as well as the biological relevance, underlying the glycolipid-Hsp70 interaction is unknown. Here we report that sulfatide promotes Hsp70 oligomerization through the N-terminal ATPase domain, which stabilizes the binding of Hsp70 to unfolded protein in vitro. We find that the Hsp70 oligomer has apparent molecular masses ranging from 440 kDa to greater than 669 kDa. The C-terminal peptide-binding domain is dispensable for the sulfatide-induced oligomer formation. The oligomer formation is impaired in the presence of ATP, while the Hsp70 oligomer, once formed, is unable to bind to ATP. These results suggest that sulfatide locks Hsp70 in a high-affinity state to unfolded proteins by clustering the peptide-binding domain and blocking the binding to ATP that induces the dissociation of Hsp70 from protein substrates.

    DOI: 10.3390/biom5020958

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  29. Discovery, primary, and crystal structures and capacitation-related properties of a prostate-derived heparin-binding protein WGA16 from boar sperm.

    Garénaux E, Kanagawa M, Tsuchiyama T, Hori K, Kanazawa T, Goshima A, Chiba M, Yasue H, Ikeda A, Yamaguchi Y, Sato C, Kitajima K

    The Journal of biological chemistry   290 巻 ( 9 ) 頁: 5484 - 501   2015年2月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    Mammalian sperm acquire fertility through a functional maturation process called capacitation, where sperm membrane molecules are drastically remodeled. In this study, we found that a wheat germ agglutinin (WGA)-reactive protein on lipid rafts, named WGA16, is removed from the sperm surface on capacitation. WGA16 is a prostate-derived seminal plasma protein that has never been reported and is deposited on the sperm surface in themalereproductive tract. BasedonproteinandcDNAsequences for purified WGA16, it is a homologue of human zymogen granule protein16(ZG16) belonging to the Jacalin-related lectin (JRL) family in crystal and primary structures. A glycan array shows that WGA16 binds heparin through a basic patch containing Lys-53/ Lys-73 residues but not the conventional lectin domain of the JRL family. WGA16 is glycosylated, contrary to other ZG16 members, and comparative mass spectrometry clearly shows its unique N-glycosylation profile among seminal plasma proteins. It has exposed GlcNAc and GalNAc residues without additional Gal residues. The GlcNAc/GalNAc residues can work as binding ligands foraspermsurface galactosyltransferase,whichactually galactosylatesWGA16in situ in the presence of UDP-Gal. Interestingly, surface removal of WGA16 is experimentally induced by either UDPGal or heparin. In the crystal structure, N-glycosylated sites and a potential heparin-binding site face opposite sides. This geography of two functional sites suggest that WGA16 is deposited on the sperm surface through interaction between its N-glycans and the surface galactosyltransferase, whereas its heparin-binding domain may be involvedinbindingto sulfatedglycosaminoglycansinthefemaletract, enabling removal ofWGA16from the sperm surface.

    DOI: 10.1074/jbc.M114.635268

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  30. Adaptive evolution of the promoter region of the Sialyltransferase 8B (STX) gene

    Fujito Naoko T., Hayakawa Toshiyuki, Hane Masaya, Kitajima Ken, Sato Chihiro, Satta Yoko

    GENES & GENETIC SYSTEMS   89 巻 ( 6 ) 頁: 327 - 327   2014年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  31. An anti-schizophrenic drug affects the surface expression of polySia-NCAM in IMR-32 human neuroblastoma cells

    Nishimura Saki, Hane Masaya, Niimi Yuki, Kitajima Ken, Sato Chihiro

    GLYCOBIOLOGY   24 巻 ( 11 ) 頁: 1193 - 1193   2014年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  32. Insight into single nucleotide polymorphisms (SNPs) of the polysialyltransferase ST8SIA2/STX in psychiatric disorders

    Hane Masaya, Nishimura Saki, Hayakawa Toshiyuki, Kitajima Ken, Sato Chihiro

    GLYCOBIOLOGY   24 巻 ( 11 ) 頁: 1206 - 1206   2014年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  33. The Synthesis of Sialo-containing Glycopolymers by pi-Allyl Nickel Catalyzed Coordination Polymerization

    Ohira Shuichi, Yasuda Yu, Sato Chihiro, KItajima Ken, Tomita Ikuyoshi, Takahashi Takashi, Tanaka Hiroshi

    GLYCOBIOLOGY   24 巻 ( 11 ) 頁: 1119 - 1120   2014年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  34. Polysialic acid: Biosynthesis, novel functions and applications

    Colley Karen J., Kitajima Ken, Sato Chihiro

    CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY   49 巻 ( 6 ) 頁: 498 - 532   2014年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Critical Reviews in Biochemistry and Molecular Biology  

    As an anti-adhesive, a reservoir for key biological molecules, and a modulator of signaling, polysialic acid (polySia) is critical for nervous system development and maintenance, promotes cancer metastasis, tissue regeneration and repair, and is implicated in psychiatric diseases. In this review, we focus on the biosynthesis and functions of mammalian polySia, and the use of polySia in therapeutic applications. PolySia modifies a small subset of mammalian glycoproteins, with the neural cell adhesion molecule, NCAM, serving as its major carrier. Studies show that mammalian polysialyltransferases employ a unique recognition mechanism to limit the addition of polySia to a select group of proteins. PolySia has long been considered an anti-adhesive molecule, and its impact on cell adhesion and signaling attributed directly to this property. However, recent studies have shown that polySia specifically binds neurotrophins, growth factors, and neurotransmitters and that this binding depends on chain length. This work highlights the importance of considering polySia quality and quantity, and not simply its presence or absence, as its various roles are explored. The capsular polySia of neuroinvasive bacteria allows these organisms to evade the host immune response. While this "stealth" characteristic has made meningitis vaccine development difficult, it has also made polySia a worthy replacement for polyetheylene glycol in the generation of therapeutic proteins with low immunogenicity and improved circulating half-lives. Bacterial polysialyltransferases are more promiscuous than the protein-specific mammalian enzymes, and new studies suggest that these enzymes have tremendous therapeutic potential, especially for strategies aimed at neural regeneration and tissue repair.

    DOI: 10.3109/10409238.2014.976606

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  35. Crystal structure of anti-polysialic acid antibody single chain Fv fragment complexed with octasialic acid: insight into the binding preference for polysialic acid.

    Nagae M, Ikeda A, Hane M, Hanashima S, Kitajima K, Sato C, Yamaguchi Y

    The Journal of biological chemistry   288 巻 ( 47 ) 頁: 33784 - 33796   2013年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    Polysialic acid is a linear homopolymer of α2-8-linked sialic acids attached mainly onto glycoproteins. Cell surface polysialic acid plays roles in cell adhesion and differentiation events in a manner that is often dependent on the degree of polymerization (DP). Anti-oligo/polysialic acid antibodies have DP-dependent antigenic specificity, and such antibodies are widely utilized in biological studies for detecting and distinguishing between different oligo/polysialic acids. A murine monoclonal antibody mAb735 has a unique preference for longer polymers of polysialic acid (DP > 10), yet the mechanism of recognition at the atomic level remains unclear. Here, we report the crystal structure of mAb735 single chain variable fragment (scFv735) in complex with octasialic acid at 1.8 Å resolution. In the asymmetric unit, two scFv735 molecules associate with one octasialic acid. In both complexes of the unit, all the complementaritydetermining regions except for L3 interact with three consecutive sialic acid residues out of the eight. A striking feature of the complex is that 11 ordered water molecules bridge the gap between antibody and ligand, whereas the direct antibodyligand interaction is less extensive. The dihedral angles of the trisialic acid unit directly interacting with scFv735 are not uniform, indicating that mAb735 does not strictly favor the previously proposed helical conformation. Importantly, both reducing and nonreducing ends of the bound ligand are completely exposed to solvent. We suggest that mAb735 gains its apparent high affinity for a longer polysialic acid chain by recognizing every three sialic acid units in a paired manner. © 2013 by The American Society for Biochemistry and Molecular Biology, Inc.

    DOI: 10.1074/jbc.M113.496224

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  36. Occurrence of free deaminoneuraminic acid (KDN)-containing complex-type N-glycans in human prostate cancers

    Yabu Masahiko, Korekane Hiroaki, Hatano Koji, Kaneda Yasufumi, Nonomura Norio, Sato Chihiro, Kitajima Ken, Miyamoto Yasuhide

    GLYCOBIOLOGY   23 巻 ( 6 ) 頁: 634 - 642   2013年6月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    We previously reported on the accumulation of a substantial amount of free N-acetylneuraminic acid (Neu5Ac)-containing complex-type N-glycans in human pancreatic cancer cells (Yabu M, Korekane H, Takahashi H, Ohigashi H, Ishikawa O, Miyamoto Y. 2013. Accumulation of free Neu5Ac-containing complex-type N-glycans in human pancreatic cancers. Glycoconj J, 30(3):247-256). In the present paper, we further extend our cancer glycomic study of human prostate cancer. Specifically, we demonstrate that, in addition to the free Neu5Ac-containing N-glycans, significant amounts of free deaminoneuraminic acid (KDN, 2-keto-3-deoxy-d-glycero-d-galacto-nononic acid)-containing N-glycans had accumulated in the prostate cancer tissues from four of five patients. Indeed, in one of the four cases, the free KDN glycans accumulated as major components in prostate cancer tissue. The structures of the KDN-containing free oligosaccharides were analyzed by a variety of methods. Specifically, we used fluorescent labeling with aminopyridine combined with two-dimensional mapping, KDNase digestion and mass spectrometry to facilitate identification. The analysis also utilized newly synthesized KDN-linked oligosaccharides as standards. The prostate-specific glycans were composed of five species having the following sequence, KDN-Gal-GlcNAc-Man-Man-GlcNAc (α2,6-KDN-linked glycans being the dominant form). The most abundant free KDN-containing N-glycan was KDNα2-6Galβ1-4GlcNAcβ1-2Manα1-3Manβ1-4GlcNAc followed by KDNα2-6Galβ1-4GlcNAcβ1-2Manα1-6Manβ1- 4GlcNAc. This is the first study to show unequivocal chemical evidence for the occurrence of KDN glycoconjugates in human tissues together with their detailed structures. These oligosaccharides might be developed as tumor markers, especially for prostate cancer. © 2012 The Author.

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  37. Impact of structural aberrancy of polysialic acid and its synthetic enzyme ST8SIA2 in schizophrenia.

    Sato C, Kitajima K

    Frontiers in cellular neuroscience   7 巻 ( APR ) 頁: 61   2013年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Frontiers in Cellular Neuroscience  

    Psychiatric disorders are a group of human diseases that impair higher cognitive functions. Whole-genomic analyses have recently identified susceptibility genes for several psychiatric disorders, including schizophrenia. Among the genes reported to be involved in psychiatric disorders, a gene encoding a polysialyltransferase involved in the biosynthesis of polysialic acid (polySia or PSA) on cell surfaces has attracted attention for its potential role in emotion, learning, memory, circadian rhythm, and behaviors. PolySia is a unique polymer that spatio-temporally modifies neural cell adhesion molecule (NCAM) and is predominantly found in embryonic brains, although it persists in areas of the adult brain where neural plasticity, remodeling of neural connections, or neural generation is ongoing, such as the hippocampus, subventricular zone, thalamus, prefrontal cortex, and amygdala. PolySia is thought to be involved in the regulation of cell-cell interactions; however, recent evidence suggests that it is also involved in the functional regulation of ion channels and neurologically active molecules, such as BDNF, FGF2, and dopamine that are deeply involved in psychiatric disorders. In this review, the possible involvement of polysialyltransferase (ST8SIA2/ST8SiaII/STX/Siat8B) and its enzymatic product, polySia, in schizophrenia is discussed. © 2013 Sato and Kitajima.

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  38. ポリシアル酸による神経機能の調節. 実験医学 31巻 10号 (増刊) pp. 26-33; 第三の生命鎖 査読有り

    佐藤 ちひろ

    実験医学   31 巻   頁: 26 - 33   2013年

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    掲載種別:研究論文(学術雑誌)  

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  39. Sialome analysis of the cephalochordate Branchiostoma belcheri, a key organism for vertebrate evolution

    Guerardel Yann, Chang Lan-Yi, Fujita Akiko, Coddeville Bernadette, Maes Emmanuel, Sato Chihiro, Harduin-Lepers Anne, Kubokawa Kaoru, Kitajima Ken

    GLYCOBIOLOGY   22 巻 ( 4 ) 頁: 479 - 491   2012年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    Sialic acid, a common terminal substitution of glycoconjugates, has been so far consistently identified in all vertebrates as well as in a growing number of bacterial species. It is assumed to be widely distributed among animal species of the deuterostome phylum, based on its identification in few echinoderm and all vertebrate species. However, whole sections of deuterostome, especially those intermediate species between invertebrates and vertebrates including cephalochordates, urochordates and hemichordates, are still unexplored in term of sialylation capacities. The discovery of functional sialic acid machinery in some of these species may shed new light onto the evolution of glycosylation capacities in deuterostome lineage. In a first approach, we investigated the sialylation pattern of a cephalocordate species, Branchiostoma belcheri, which occupies a strategic phylogenetic position to understand the transition of invertebrates toward vertebrates. Structural analysis of B. belcheri glycoconjugates established that this organism synthesizes large quantities of various sialic acids, some of which present rare or novel structures such as methylated sialic acids. These sialic acids were shown to be mainly associated with mono-and disialylated core 1-type O-glycans. Moreover, screening of the animal organs revealed the existence of exquisite tissue specificity in the distribution of sialic acids. Description of sialylation profiles was then correlated with the expression patterns of key enzymes involved in the biosynthesis of major forms of sialic acids, which provides the first complete overview of the sialylation patterns in cephalochordates. © 2011 The Author.

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  40. Structural and functional impairments of polysialic acid (polySia)-neural cell adhesion molecule (NCAM) synthesized by a mutated polysialyltransferase of a schizophrenic patient

    Hane Masaya, Sumida Mizuki, Kitajima Ken, Sato Chihiro

    PURE AND APPLIED CHEMISTRY   84 巻 ( 9 ) 頁: 1895 - 1906   2012年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Pure and Applied Chemistry  

    Polysialic acid (polySia) is a homopolymer of sialic acid with a degree of polymerization (DP) of 8-100. When present on neural cell adhesion molecule (NCAM), polySia has anti-adhesive effects on cell-cell interactions owing to its bulky polyanionic nature, and is involved in the regulation of neurogenesis and neuronal functions. Recently, we demonstrated that polySia functions not only as an anti-cell adhesion molecule, but also as a reservoir scaffold for brain-derived neurotrophic factor (BDNF) and fibroblast growth factor 2 (FGF2), which are biologically active molecules in neurogenesis. To understand the significance of polySia structure in the reservoir function, we focused on polySia-NCAM biosynthesized by mutated polysialyltransferase (ST8SiaII or STX) that was reported in a schizophrenia patient. The polySia-NCAM biosynthesized by mutant ST8SiaII/STX contained less polySia with shorter chain length and exhibited impaired reservoir function for BDNF and FGF2 as compared with that synthesized by wild-type (wt) ST8SiaII/STX. Our findings suggest that the quantity and quality of polySia on NCAM are important for normal neuronal functioning. © 2012 IU PAC.

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  41. Co-expression of two distinct polysialic acids, α2,8- and α2,9-linked polymers of N-acetylneuraminic acid, in distinct glycoproteins and glycolipids in sea urchin sperm.

    Miyata S, Yamakawa N, Toriyama M, Sato C, Kitajima K

    Glycobiology   21 巻 ( 12 ) 頁: 1596 - 605   2011年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    Naturally occurring polysialic acid (polySia) structures have a large diversity, primarily arising from the diversity in the sialic acid components as well as in the intersialyl linkages. In 2004, we demonstrated the presence of a new type of polySia, 8-O-sulfated N-acetylneuraminic acid (Neu5Ac) capped α2,9-linked polyNeu5Ac, on the O-glycans of a major 40-80 kDa sialoglycoprotein, flagellasialin, in sea urchin sperm. In this study, we demonstrated that another type of polySia, the α2,8-linked polyNeu5Ac, exclusively occurs on O-glycans of a 190 kDa glycoprotein (190 kDa-gp), whereas the α2,9-linked polyNeu5Ac is exclusively present on flagellasialin. The 190 kDa-gp is localized in both flagellum and head of sperm. We also demonstrated that polysialogangliosides containing the α2,8-linked polyNeu5Ac are present in sperm head. Thus, this study shows two novel features of the occurrence of polySia in nature, the co-localization of polySia with different intersialyl linkages, the α2,8-and α2,9-linkages, in a single cell and the occurrence of α2,8-linked polyNeu5Ac in glycolipids. Anti-α2,8-linked polyNeu5Ac antibody had no effect on fertilization, which contrasted with the previous results that anti-α2,9-linked polyNeu5Ac antibody inhibited sperm motility and fertilization. Based on these properties, distinct functions of α2,8-and α2,9-polySia structures are implicated in fertilization. © 2011 The Author.

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  42. New Functions of Polysialic Acid and Its Relationship to Schizophrenia

    Sato Chihiro, Kitajima Ken

    TRENDS IN GLYCOSCIENCE AND GLYCOTECHNOLOGY   23 巻 ( 133 ) 頁: 221 - 238   2011年9月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Trends in Glycoscience and Glycotechnology  

    Polysialic acid (polySia), particularly α2,8-linked polyNeu5Ac (DP=8~400), is a unique polymer that spatiotemporally modifies neural cell adhesion molecule (NCAM), predominantly in embryonic brains. PolySia is considered to function as a negative regulator of adhesion between cells, and between cells and extracellular matrix due to its extremely polyanionic nature and steric hindrance. Through its antiadhesive property and spatio-temporal expression, polySia is involved in cell migration, neural outgrowth, axonal guidance, synaptic plasticity, and the development of normal neural circuits and neurogenesis. Due to improvements of polySiadetection methods, it has been shown that polySia expression persists in the hippocampus and olfactory bulb of adults, where neurogenesis is ongoing; however, the functions of polySia, particularly in adult brains, remain incompletely resolved. Recently, we demonstrated that polySia functions not only as an anti-adhesive molecule, but also as a reservoir for specific bioactive molecules, such as neurotrophic factors, neurotransmitters, and growth factors, which regulate neural function. In addition, studies have revealed that the enzymatic activity of STX, which is involved in the synthesis of polySia, derived from schizophrenic patient is low and that the product of the enzyme, polySia on NCAM is impaired with respect to both quantity and quality. Notably, impaired polySia-NCAM cannot effectively retain bioactive molecules, including BDNF, dopamine, and FGF2. Taken together, the impairment of polySia might influence the retention function of polySia and lead to the development of psychiatric disorders, such as schizophrenia, which are reported to express either lower or elevated amounts of polySia compared with normal brains. ©2011 FCCA.

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  43. Structural and functional impairments of polysialic acid by a mutated polysialyltransferase found in schizophrenia.

    Isomura R, Kitajima K, Sato C

    The Journal of biological chemistry   286 巻 ( 24 ) 頁: 21535 - 45   2011年6月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    Polysialic acid (polySia), a unique acidic glycan modifying neural cell adhesion molecule (NCAM), is known to regulate embryonic neural development and adult brain functions. Polysialyltransferase STX is responsible for the synthesis of polySia, and two single nucleotide polymorphisms (SNPs) of the coding region of STX are reported from schizophrenic patients: SNP7 and SNP9, respectively, giving STX(G421A) with E141K and STX(C621G) with silent mutations. In this study, we focused on these mutations and a binding activity of polySia to neural materials, such as brain-derived neurotrophic factor (BDNF). Here we describe three new findings. First, STX(G421A) shows a dramatic decrease in polySia synthetic activity on NCAM, whereas STX(C621G) does not. The STX(G421A)-derived polySia-NCAM contains a lower amount of polySia with a shorter chain length. Second, polySia shows a dopamine (DA) binding activity, which is a new function of polySia as revealed by frontal affinity chromatography for measuring the polySia-neurotransmitter interactions. Interestingly, the STX(G421A)-derived polySia-NCAM completely loses the DA binding activity, whereas it greatly diminishes but does not lose the BDNF binding activity. Third, an impairment of the polySia structure with an endosialidase modulates the DA-mediated Akt signaling. Taken together, impairment of the amount and quality of polySia may be involved in psychiatric disorders through impaired binding to BDNF and DA, which are deeply involved in schizophrenia and other psychiatric disorders, such as depression and bipolar disorder. © 2011 by The American Society for Biochemistry and Molecular Biology, Inc.

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  44. IgG2 dominancy and carbohydrate recognition specificity of C3H/He mouse antibodies directed to cross-reactive carbohydrate determinants (CCDs) bearing beta-(1,2)-xylose and alpha-(1,3)-fucose.

    Hino S, Umeda F, Inumaru S, Aoki N, Sato C, Okajima T, Nadano D, Matsuda T

    Immunology letters   133 巻 ( 1 ) 頁: 28 - 34   2010年9月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Immunology Letters  

    Few common carbohydrate epitopes consisting of terminal β-(1,2)-xylose and/or α-(1,3)-fucose residues are shared by a variety of glycoproteins from plants, insects and parasitic worms, termed cross-reactive carbohydrate determinant (CCD), and frequently recognized by IgE antibodies of patients with food and/or respiratory allergy, though clinical relevancy of such CCD-specific IgE is still controversial. Attention has also been focused on CCDs from the undesired post-translational modification of recombinant therapeutic proteins produced by transgenic plants and insects. In the present study, to clarify immunogenic potentials of CCD-bearing glycoproteins, the antibody response to a model plant glycoprotein, horseradish peroxidase (HRP) was investigated in a mouse model. C3H/He mice were immunized with HRP plus Al(OH)3 or Freund's adjuvant, and IgG and IgE responses to CCDs in addition to HRP were analyzed by ELISA using some distinct glycoproteins with known N-glycan structures. IgE response to HRP was induced remarkably, whereas that to CCD was weaker and delayed. Moreover, apparent ratio of the CCD-specific antibodies to HRP-specific ones tended to be higher in IgG2a and IgG2b isotypes than IgG1, IgG3 and IgE. In contrast to rabbit antibodies, the CCD-specific antibodies from the mice gave poor reactivity with bromelain and honeybee phospholipase A2, suggesting the critical role of both β-(1,2)-xylose and α-(1,3)-mannose in the CCD-recognition by the mouse antibodies. Moreover, the mouse antibodies showed weaker cross-reactivity to pollen- and insect-derived glycoproteins than the rabbit ones. Thus, in this mouse model, not only IgE but also IgG2 antibody responses to CCDs were induced by immunizing with a CCD-bearing glycoprotein, suggesting that CCDs affected not only Th2-type but also Th1-type antibody response at least in C3H/He mice. © 2010 Elsevier B.V.

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  45. Extensive enrichment of N-glycolylneuraminic acid in extracellular sialoglycoproteins abundantly synthesized and secreted by human cancer cells.

    Inoue S, Sato C, Kitajima K

    Glycobiology   20 巻 ( 6 ) 頁: 752 - 62   2010年6月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    N-Glycolylneuraminic acid (Neu5Gc) is the second most populous sialic acid (Sia). The only known biosynthetic pathway of Neu5Gc is the hydroxylation of cytidine-5′monophosphate-N-acetylneuraminic acid (CMP-Neu5Ac), catalyzed by CMP-Neu5Ac hydroxylase (CMAH). Neu5Gc is abundantly found in mammals except for human, in which CMAH is inactivated due to mutation in the CMAH gene. Evidence has accumulated to show occurrence of Neu5Gc-containing glycoconjugates in sera of cancer patients, human cancerous tissues and cultured human cell lines. Recently, occurrence of natural antibodies against Neu5Gc was shown in healthy humans and is a serious problem for clinical xenotransplantation and stem cell therapies. Studying human occurrence of Neu5Gc is of importance and interest in a broad area of medical sciences. In this study, using a fluorometric high performance liquid chromatography method, we performed quantitative analyses of Sias both inside and in the external environment of the cell and found that (i) incorporation of Neu5Gc was most prominent in soluble glycoproteins found both in the extracellular space and inside the cell as the major Sia compounds. (ii) Of the total Neu5Gc in the Sia compounds that the cells synthesized, 90% was found in the secreted sialoglycoproteins, whereas for Neu5Ac, 70% was found in the secreted sialoglycoproteins. (iii) The Neu5Gc ratio was higher in the secreted sialoglycoproteins (as high as 40% of total Sias) than in intracellular sialoglycoproteins. (iv) The majority of the secreted sialoglycoproteins was anchored on the culture dishes and solubilized by brief trypsin treatment. Based on these findings, a new idea on the mechanism of accumulation of Neu5Gc in cancer cells was proposed. © The Author 2010. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org.

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  46. 特集 糖鎖のかかわる病気:発症機構,診断,治療に向けて 糖鎖と統合失調症

    佐藤 ちひろ

    生体の科学   61 巻 ( 2 ) 頁: 160 - 166   2010年4月

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    掲載種別:研究論文(学術雑誌)   出版者・発行元:株式会社医学書院  

    DOI: 10.11477/mf.2425100979

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  47. Measurement of glycan-based interactions by frontal affinity chromatography and surface plasmon resonance.

    Sato C, Yamakawa N, Kitajima K

    Methods in enzymology   478 巻 ( C ) 頁: 219 - 32   2010年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Methods in Enzymology  

    Proteins and lipids are often modified with glycan chains, which due to their large hydration effect and structural heterogeneity, significantly alter the surface physicochemical properties of proteins and biomembranes. This "glyco-atmosphere" also serves as a field for interactions with various molecules, including other glycans, lipids, peptides, proteins, and small molecules such as neurotransmitters and drugs as well as lectins. Therefore, sensitive techniques for measuring these glycan-based interactions are becoming more and more necessary, with the appropriate method largely depending on the interacting molecules. In this chapter, we focus on frontal affinity chromatography (FAC) and surface plasmon resonance (SPR) for examining polysialic acid-involved interactions with neurotransmitters and neurotrophins. FAC is characterized by its applicability to analyze weak interactions that are difficult to measure using conventional methods, and by the ease of principle and experimental procedures. SPR is advantageous due to the availability of suitable surface materials and for real-time monitoring with nonlabeled analytes. © 2010 Elsevier Inc.

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  48. 糖鎖と統合失調症

    佐藤 ちひろ

    生体の科学 61     頁: 160 - 166   2010年

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    掲載種別:研究論文(学術雑誌)  

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  49. Complex formation of a brain-derived neurotrophic factor and glycosaminoglycans.

    Kanato Y, Ono S, Kitajima K, Sato C

    Bioscience, biotechnology, and biochemistry   73 巻 ( 12 ) 頁: 2735 - 41   2009年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Bioscience, Biotechnology and Biochemistry  

    Glycosaminoglycans (GAGs), large anionic glycopolymers, are the glycan portion of proteoglycans and are important components of the extracellular matrix. Recently we reported that polysialic acid, a polyanionic glycopolymer specific to the brain, binds neurotrophic factors to form a large complex. It is not clear whether GAGs also bind neurotrophic factors to form a large complex. In the present study, we demonstrate that a brain-derived neurotrophic factor (BDNF) dimer directly binds GAGs other than chondroitin and hyaluronic acid to form a large complex. Neurotrophin-3 showed similar GAG binding properties. Furthermore, BDNF, after forming a large complex with GAG, bound to the BDNF receptors tropomyosin-related kinase (Trk) B and p75 neurotrophin receptor (NTR). These findings suggest that GAGs function to produce a reservoir of BDNF and other neurotrophic factors, and may serve to regulate their local concentrations on the cell surface.

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  50. Developmental regulation of oligosialylation in zebrafish

    Chang Lan-Yi, Harduin-Lepers Anne, Kitajima Ken, Sato Chihiro, Huang Chang-Jen, Khoo Kay-Hooi, Guerardel Yann

    GLYCOCONJUGATE JOURNAL   26 巻 ( 3 ) 頁: 247 - 261   2009年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycoconjugate Journal  

    Zebrafish appears as a relevant model for the functional study of glycoconjugates along vertebrate's development. Indeed, as a prelude to such studies, we have previously identified a vast array of potentially stage-specific glycoconjugates, which structures are reminiscent of glycosylation pathways common to all vertebrates. In the present study, we have focused on the identification and regulation of major protein and lipids associated α2-8-linked oligosialic acids motifs in the early development of zebrafish. By a combination of partial hydrolysis, anion exchange HPLC-FD and mass spectrometry, we demonstrated that glycoproteins and glycolipids differed by the extent and the nature of their substituting oligosialylated sequences. Furthermore, relative quantifications showed that α2-8-linked sialylation was differentially regulated in both families of glycoconjugates along development. Accordingly, we established that α2,8-sialyltransferase mRNA levels was directly correlated with changes of α2,8-sialylation status of glycolipids, but independent of those observed on major glycoproteins that appear to originate from the mother. © 2008 Springer Science+Business Media, LLC.

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  51. Membrane microdomains from early gastrula embryos of medaka, Oryzias latipes, are a platform of E-cadherin- and carbohydrate-mediated cell-cell interactions during epiboly.

    Adachi T, Sato C, Kishi Y, Totani K, Murata T, Usui T, Kitajima K

    Glycoconjugate journal   26 巻 ( 3 ) 頁: 285 - 99   2009年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycoconjugate Journal  

    Formation of membrane microdomain is critical for cell migration (epiboly) during gastrulation of medaka fish [Adachi et al. (Biochem. Biophys. Res. Commun. 358:848-853, 2007)]. In this study, we characterized membrane microdomain from gastrula embryos to understand its roles in epiboly. A cell adhesion molecule (E-cadherin), its associated protein (β-catenin), transducer proteins (PLCγ, cSrc), and a cytoskeleton protein (β-actin) were enriched in the membrane microdomain. LeX- containing glycolipids and glycoproteins (LeX-gp) were exclusively enriched in the membrane microdomain. Interestingly, the isolated membrane microdomain had the ability to bind to each other in the presence of Ca 2+. This membrane microdomain binding was achieved through the E-cadherin homophilic and the LeX-glycan-mediated interactions. E-cadherin and LeX-gp were co-localized on the same membrane microdomain, suggesting that these two interactions are operative at the same time. Thus, the membrane microdomain functions as a platform of the E-cadherin- and LeX-glycan-mediated cell adhesion and signal transduction. © 2008 Springer Science+Business Media, LLC.

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  52. 3P-066 シアル酸結合免疫グロブリン様レクチン(シグレック)-7によるシアロ糖鎖認識の生化学的および分子ドッキング解析(蛋白質-機能(反応機構,生物活性など),第47回日本生物物理学会年会)

    生物物理   49 巻 ( supplement ) 頁: S162   2009年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:一般社団法人 日本生物物理学会  

    DOI: 10.2142/biophys.49.s162_2

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  53. Direct binding of polysialic acid to a brain-derived neurotrophic factor depends on the degree of polymerization.

    Kanato Y, Kitajima K, Sato C

    Glycobiology   18 巻 ( 12 ) 頁: 1044 - 53   2008年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    Polysialic acid (polySia) is the homopolymer of sialic acid and negatively regulates neuronal cell-cell and cell-extracellular matrix interactions through steric and repulsive hindrance due to its bulky polyanionic structure. Whether polySia also functions as a positive regulator in the nervous system through binding to specific ligands is not known. In the present study, we demonstrated that a brain-derived neurotrophic factor (BDNF) dimer binds directly to polySia to form a large complex with an Mr greater than 2000 kDa under physiologic conditions. Although somewhat affected by the linkage and type of sialic acid components in the polySia, the complex formation is highly dependent on the polySia chain length. The minimum degree of polymerization required for the complex formation is 12. This is the first study to demonstrate the biologic significance of the degree of polySia polymerization in eukaryotes. Similar large polySia complexes form with other neurotrophic factors such as nerve growth factor, neurotrophin-3, and neurotrophin-4. Furthermore, the BDNF, after making a complex with polySia, can bind to the BDNF receptors, TrkB and p75NTR. The complex formation of BDNF with polySia upregulates growth or/and survival of neuroblastoma cells. These findings suggest that polySia functions as a reservoir of BDNF and other neurotrophic factors and may serve to regulate their local concentrations on the cell surface. © The Author 2008. Published by Oxford University Press. All rights reserved.

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  54. ポリシアル酸構造による細胞シグナルの調節機構

    佐藤 ちひろ

    北島健蛋白質核酸酵素 53     頁: 1577 - 1583   2008年

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    掲載種別:研究論文(学術雑誌)  

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  55. ポドシアル酸構造による細胞シグナルの調節機構.

    佐藤 ちひろ

    蛋白質核酸酵素 53     頁: 1577 - 1583   2008年

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    掲載種別:研究論文(学術雑誌)  

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  56. Development of sensitive chemical and immunochemical methods for detecting sulfated sialic acids and their application to glycoconjugates from sea urchin sperm and eggs.

    Yamakawa N, Sato C, Miyata S, Maehashi E, Toriyama M, Sato N, Furuhata K, Kitajima K

    Biochimie   89 巻 ( 11 ) 頁: 1396 - 408   2007年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochimie  

    Sulfated sialic acid (SiaS) is a unique sialic acid (Sia) derivative in which an additional anionic group is attached to a carboxylated monosaccharide. Very little is known about the occurrence and biologic function of SiaS, due to the limitations of analytical methods to detect it in minute amounts. In this study, to develop methods and probes for detecting and pursuing the functions of SiaS, we developed sensitive chemical and immunochemical detection methods. First, we synthesized as model compounds 4-methylumbelliferyl glycosides of 8-O- and 9-O-sulfated Sia consisting of N-acetylneuraminic acid (Neu5Ac), N-glycolylneuraminic acid (Neu5Gc), and deaminoneuraminic acid (Kdn). Second, we applied fluorometric high performance liquid chromatography (HPLC) analysis to these synthetic glycosides. After acid hydrolysis of the samples, the liberated SiaS were labeled with a fluorescent reagent, 1,2-diamino-4,5-methylenedioxybenzene, and analyzed on fluorometric HPLC. We established an optimal elution condition for successful separation of 8-O- and 9-O-sulfated Neu5Ac, Neu5Gc, and Kdn on HPLC. Third, we generated a monoclonal antibody (mAb) 2C4 against SiaS using sea urchin egg components as the immunogen. mAb.2C4 recognizes both 8-O-sulfated Neu5Ac (Neu5Ac8S) and Neu5Gc8S, whereas the previously prepared mAb.3G9 only recognizes Neu5Ac8S. Finally, using the fluorometric HPLC and monoclonal antibodies, we demonstrated that glycoconjugates from sea urchin sperm exclusively contained Neu5Ac8S, whereas those from eggs contained Neu5Gc8S. Furthermore, we clarified the quantitative differences in the SiaS content in eggs and sperm from two different species of sea urchins. Immunostaining using mAb.2C4 showed that Neu5Gc8S is localized in the cortical granules in unfertilized eggs, whereas it is localized in the outer surface of the fertilization layer as well as in the inner surface of fertilized eggs. Thus, 8-O-sulfation is dependent on the species, gametic cell-type, site-localization of the eggs, and glycoconjugates. © 2007 Elsevier Masson SAS. All rights reserved.

    DOI: 10.1016/j.biochi.2007.04.010

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  57. The rainbow trout CMP-sialic acid synthetase utilises a nuclear localization signal different from that identified in the mouse enzyme

    Tiralongo Joe, Fujita Akiko, Sato Chihiro, Kitajima Ken, Lehmann Friederike, Oschlies Melanie, Gerardy-Schahn Rita, Muenster-Kuehnel Anja K.

    GLYCOBIOLOGY   17 巻 ( 9 ) 頁: 945 - 954   2007年9月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    The terminal sugar sialic acid (Sia) plays a pivotal role in cell-cell interaction and recognition. A prerequisite for the biosynthesis of sialoglycoconjugates is the activation of Sia to cytidine monophosphate-Sia (CMP-Sia), by CMP-Sia synthetases (CMP-Sia-syn). CMP-Sia-syn are conserved from bacteria to man, and have been found to reside in the nucleus of all vertebrate species analysed to date. We previously cloned the CMP-Sia-syn from rainbow trout (rt) and identified three clusters of basic amino acids (BC) that might act as nuclear localization signals (NLS). Here, we utilised chimeric proteins and rt CMP-Sia-syn mutants in which putative NLS sequences were deleted, to identify the nuclear transport signal. Divergent from the mouse enzyme, where the crucial NLS is part of the enzyme's active site, in the rt CMP-Sia-syn the NLS and active site are disparate. The crucial NLS in the fish enzyme is bipartite and the functionality depends on a free N-terminus. Comparative analysis of all putative rt NLS in mouse and fish cells identified a second inferior motif (rtBC5-6), which was functional only in fish cells suggesting some differences in transport mechanism or folding variabilities in fish. Moreover, based on computational analyses of putative CMP-Sia-syn from distant deuterostomian organisms it was concluded that CMP-Sia-syn nuclear localization is a relatively recent invention, originating in echinoderms. In summary, our data describing structural differences in the NLS of vertebrate CMP-Sia-syn, and the independence of Sia activation from the subcellular localization of the enzyme, provide supporting evidence that nuclear localization is linked to a second yet unknown function. © The Author 2007. Published by Oxford University Press. All rights reserved.

    DOI: 10.1093/glycob/cwm064

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  58. Membrane microdomain formation is crucial in epiboly during gastrulation of medaka.

    Adachi T, Sato C, Kitajima K

    Biochemical and biophysical research communications   358 巻 ( 3 ) 頁: 848 - 53   2007年7月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical and Biophysical Research Communications  

    Membrane microdomain (microdomain) was isolated from early gastrula embryos. The isolated microdomain was characterized by enrichment of cholesterol and sphingomyelin, and by the presence of huge glycoproteins containing Lewis X structure. Importance of the microdomain in the progress of epiboly was assessed using methyl β-cyclodextrin (MBCD) and C2-ceramide that disrupt microdomains through different mechanisms. Both reagents efficiently disrupted the microdomain structure and concomitantly impaired epiboly. Interestingly, when embryos pretreated with MBCD, a cholesterol-binding molecule, were exogenously supplemented with cholesterol, the embryos underwent not only reconstitution of the microdomain, but also complete restoration to the normal epiboly. Thus, normal or impaired development is reversibly controlled by the cholesterol-dependent formation or disruption of microdomains. The most typical phenotype of the microdomain-disrupted embryos is detachment of cells from the blastoderm, suggesting that a major contribution of microdomains to epiboly is cell adhesion of blastodermal cells. © 2007 Elsevier Inc. All rights reserved.

    DOI: 10.1016/j.bbrc.2007.04.197

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  59. Hypoxia-enhanced expression of free deaminoneuraminic acid in human cancer cells.

    Go S, Sato C, Yin J, Kannagi R, Kitajima K

    Biochemical and biophysical research communications   357 巻 ( 2 ) 頁: 537 - 42   2007年6月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical and Biophysical Research Communications  

    Hypoxia is a common characteristic of locally advanced tumors and cancer cells of high invasiveness and metastasis. We first demonstrate that hypoxic culture of human cancer HeLa, LS174T, and Caco-2 cells enhances the de novo synthesis of free sialic acids including deaminoneuraminic acid (Kdn), a unique sialic acid. Hypoxic cultures enhance expression of the N-acetylneuraminic acid (Neu5Ac) 9-phosphate synthetase (NPS) and phosphomannoisomerase (PMI) mRNAs and their enzymatic activities. In addition, incorporation of mannose (Man) into the cells is also enhanced. The elevated NPS activity facilitates the synthesis of Kdn as well as Neu5Ac, a typical sialic acid in human. The increased PMI activity, together with the enhanced Man-incorporation ability, leads to the increase of mannose 6-phosphate, which is a substrate of NPS, and subsequently results in the increased expression of Kdn, but not Neu5Ac. Kdn may thus be a target for diagnosis of cancers. © 2007 Elsevier Inc. All rights reserved.

    DOI: 10.1016/j.bbrc.2007.03.181

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  60. Identification of the nuclear export signals that regulate the intracellular localization of the mouse CMP-sialic acid synthetase.

    Fujita A, Sato C, Kitajima K

    Biochemical and biophysical research communications   355 巻 ( 1 ) 頁: 174 - 80   2007年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical and Biophysical Research Communications  

    The CMP-sialic acid synthetase (CSS) catalyzes the activation of sialic acid (Sia) to CMP-Sia which is a donor substrate of sialyltransferases. The vertebrate CSSs are usually localized in nucleus due to the nuclear localization signal (NLS) on the molecule. In this study, we first point out that a small, but significant population of the mouse CMP-sialic acid synthetase (mCSS) is also present in cytoplasm, though mostly in nucleus. As a mechanism for the localization in cytoplasm, we first identified two nuclear export signals (NESs) in mCSS, based on the localization studies of the potential NES-deleted mCSS mutants as well as the potential NES-tagged eGFP proteins. These two NESs are conserved among mammalian and fish CSSs, but not present in the bacterial or insect CSS. These results suggest that the intracellular localization of vertebrate CSSs is regulated by not only the NLS, but also the NES sequences. © 2007 Elsevier Inc. All rights reserved.

    DOI: 10.1016/j.bbrc.2007.01.139

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  61. Identification of an Inflammation-inducible Serum Protein Recognized by Anti-disialic Acid Antibodies as Carbonic Anhydrase II

    YASUKAWA Zenta, SATO Chihiro, KITAJIMA Ken

    Journal of Biochemistry   141 巻 ( 3 ) 頁: 429 - 441   2007年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  62. Glycobiology of polysialic acids on sea urchin gametes

    Miyata S., Sato C., Kitajima K.

    Trends in Glycoscience and Glycotechnology   19 巻 ( 106 ) 頁: 85 - 98   2007年3月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Trends in Glycoscience and Glycotechnology  

    Naturally occurring polysialic acids (polySias), a unique homopolymer of sialic acid (Sia) residues, have a large structural diversity, primarily arising from the diversities in Sia components as well as in the intersialyl linkages. The α2,8-linked polySia on the neural cell adhesion molecules (NCAM) is the most extensively studied and recognized as a regulator of cell-cell interactions during development and differentiation in vertebrate brain. However, little is known about the occurrence and functions of polySia other than the α2,8-linked polySia on NCAM. Recently, it has been shown that polySia occurs in nature more frequently than previously recognized, as analytical methods to detect polySia structures have been greatly improved. Using these methods, two different types of polySia, α2,8- and α2,9-linked polySia, have been discovered on the sea urchin sperm, although the α2,5O glycolyl-linked polySia was already known in sea urchin egg. This is the first example of the co-localization of polySia with different intersialyl linkages in the same cell. The α2,9-linked polySia-containing glycoprotein of sea urchin sperm flagella was identified and named "flagellasialin". The α2,9-linked polySia on flagellasialin is suggested as a regulator of intracellular Ca 2+ and sperm motility. In addition, the α2,50 glycolyl-linked polySia has recently been shown to increase intracellular pH and potentiate acrosome reaction of sea urchin sperm. These results indicate that these polySia structures in sea urchin gametes have new functions other than the negative regulator for the NCAM-mediated cell adhesion. In this review, we summarize the recent advances in structural and functional studies of polySia in sea urchin gametes. © 2007 FCCA.

    DOI: 10.4052/tigg.19.85

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  63. Complex formation of 70-kDa heat shock protein with acidic glycolipids and phospholipids.

    Harada Y, Sato C, Kitajima K

    Biochemical and biophysical research communications   353 巻 ( 3 ) 頁: 655 - 60   2007年2月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical and Biophysical Research Communications  

    A new property of a heat-inducible heat shock protein (Hsp) 70.1 that it forms a complex with acidic lipids was first demonstrated. Based on the behaviors of the complexes on the native PAGE, the acidic lipid/Hsp70.1 complexes are categorized into two groups. The first group is the sulfatide-induced large-sized complex, which stays on the gel top on the native PAGE. Only the N-terminal ATPase domain is responsible for the complex formation. The second group is the ganglioside-induced complex, which is diffused in the resolution gel on the native PAGE. Both the N-terminal ATPase and the C-terminal peptide-binding domains are involved in the complex formation. No complex is formed by neutral glyco- and phospholipids. The complex formation with the acidic glyco- and phospholipids implicates the various functions of Hsp70 on the membrane surfaces. © 2006 Elsevier Inc. All rights reserved.

    DOI: 10.1016/j.bbrc.2006.12.068

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  64. Polysialic acid on flagellasialin is involved in sperm motility

    Miyata Shinji, Sato Chihiro, Kumita Hironobu, Toriyama Masaru, Kitajima Ken

    ZOOLOGICAL SCIENCE   23 巻 ( 12 ) 頁: 1171 - 1171   2006年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  65. Involvement of the α2,8-Polysialyltransferases II/STX and IV/PST in the Biosynthesis of Polysialic Acid Chains on the O-Linked Glycoproteins in Rainbow Trout Ovary

    Asahina Shinji, Sato Chihiro, Matsuno Midori

    The journal of biochemistry   140 巻 ( 5 ) 頁: 687 - 701   2006年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Japanese Biochemical Society  

    CiNii Research

  66. Involvement of the alpha2,8-polysialyltransferases II/STX and IV/PST in the biosynthesis of polysialic acid chains on the O-linked glycoproteins in rainbow trout ovary.

    Asahina S, Sato C, Matsuno M, Matsuda T, Colley K, Kitajima K

    Journal of biochemistry   140 巻 ( 5 ) 頁: 687 - 701   2006年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biochemistry  

    Polysialoglycoprotein (PSGP) in salmonid fish egg is a unique glycoprotein bearing α2,8-linked polysialic acid (polySia) on its O-linked glycans. Biosynthesis of the polySia chains is developmentally regulated and only occurs at later stage of oogenesis. Two α2,8-polysialyltransferases (α2,8-polySTs), PST (ST8Sia IV) and STX (ST8Sia II), responsible for the biosynthesis of polySia on N-glycans of glycoproteins, are known in mammals. However, nothing has been known about which α2,8-polySTs are involved in the biosynthesis of polySia on O-linked glycans in any glycoproteins. We thus sought to identify cDNA encoding the α2,8-polyST involved in polysialylation of PSGP. A clone for PST orthologue, rtPST, and two clones for the STX orthologue, rtSTX-ov and rtSTX-em, were identified in rainbow trout. The deduced amino acid sequence of rtPST shows a high identity (72-77%) to other vertebrate PSTs, while that of rtSTX-ov shows 92% identity with rtSTX-em and a significant identity (63-76%) to other vertebrate STXs. The rtPST exhibited the in vivo α2,8-polyST activity, although its in vitro activity was low. However, the rtSTXs showed no in vivo and very low in vitro activities. Interestingly, co-existence of rtPST and rSTX-ov in the reaction mixture synergistically enhanced the α2,8-polyST activity. During oogenesis, rtPST was constantly expressed, while the expression of rtSTX-ov was not increased until polySia chain is abundantly biosynthesized in the later stage. rtSTX-em was not expressed in ovary. These results suggest that the enhanced expression of rtSTX-ov under the co-expression with rtPST may be important for the biosynthesis of polySia on O-linked glycans of PSGP. © 2006 The Japanese Biochemical Society.

    DOI: 10.1093/jb/mvj200

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  67. Oral ingestion of mannose alters the expression level of deaminoneuraminic acid (KDN) in mouse organs.

    Go S, Sato C, Furuhata K, Kitajima K

    Glycoconjugate journal   23 巻 ( 5-6 ) 頁: 411 - 21   2006年7月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycoconjugate Journal  

    Deaminoneuraminic acid (KDN) is a unique member of the sialic acid family. We previously demonstrated that free KDN is synthesized de novo from mannose as its precursor sugar in trout testis, and that the amount of intracellular KDN increases in mouse B16 melanoma cells cultured in mannose-rich media [Angata et al. (1999) J. Biol. Chem. 274, 22949-56; Angata et al. (1999) Biochem. Biophys. Res. Commun. 261, 326-31]. In the present study, we first demonstrated a mannose-induced increase in intracellular KDN in various cultured mouse and human cell lines. These results led us to examine whether KDN expression in mouse organs is altered by exogenously administered mannose. Under normal feeding conditions, intracellular free KDN was present at very low levels (19-48 pmol/mg protein) in liver, spleen, and lung, and was not detected in kidney or brain. Oral ingestion of mannose, both short-term (90 min) and long-term (2 wk), resulted in an increase of intracellular KDN up to 60-81 pmol/mg protein in spleen and lung and 6.9-18 pmol/mg protein in kidney and brain; however, no change was observed in liver. The level of KDN in organs appears not to be determined only by the KDN 9-phosphate synthase activity, but might also be affected by other enzymes that utilize mannose 6-phosphate as a substrate as well as the enzymes that breakdown KDN, like KDN-pyruvate lyase. In blood, the detectable amount of free KDN did not change on oral ingestion of mannose. These findings indicate that mannose in the diet affects KDN metabolism in various organs, and provide clues to the mechanism of altered KDN expression in some tumor cells and aged organs. © Springer Science + Business Media, LLC 2006.

    DOI: 10.1007/s10719-006-6734-z

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  68. Weaning-induced expression of a milk-fat globule protein, MFG-E8, in mouse mammary glands, as demonstrated by the analyses of its mRNA, protein and phosphatidylserine-binding activity.

    Nakatani H, Aoki N, Nakagawa Y, Jin-No S, Aoyama K, Oshima K, Ohira S, Sato C, Nadano D, Matsuda T

    The Biochemical journal   395 巻 ( 1 ) 頁: 21 - 30   2006年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical Journal  

    A milk membrane glycoprotein, MFG-E8 [milk fat globule-EGF (epidermal growth factor) factor 8], is expressed abundantly in lactating mammary glands in stage- and tissue-specific manners, and has been believed to be secreted in association with milk fat globules. In the present paper, we describe further up-regulation of MFG-E8 in involuting mammary glands, where the glands undergo a substantial increase in the rate of epithelial cell apoptosis, and a possible role of MFG-E8 in mediating recognition and engulfment of apoptotic cells through its specific binding to PS (phosphatidylserine). Immunoblotting and RNA blotting analyses revealed that both MFG-E8 protein and MFG-E8 mRNA were markedly increased in mammary tissue within 3 days of either natural or forced weaning (pup withdrawal) of lactating mice. Using immunohistochemical analysis of the mammary tissue cryosections, the MFG-E8 signal was detected around the epithelium of such involuting mammary glands, but was almost undetectable at early- and mid-lactation stages, although strong signals were obtained for milk fat globules stored in the alveolar lumen. Some signals double positive to a macrophage differentiation marker, CD68, and MFG-E8 were detected in the post-weaning mammary tissue, although such double-positive signals were much smaller in number than the MFG-E8 single-positive ones. Total MFG-E8 i n milk was also increased in the post-weaning mammary glands and, furthermore, the free MFG-E8 content in the post-weaning milk, as measured by in vitro PS-binding and apoptotic HC11 cell-binding activities, was much higher than that of lactation. In addition, the post-weaning milk enhanced the binding of apoptotic HC11 cells to J774 macrophages. Sucrose density-gradient ultracentrifugation analyses revealed that such enhanced PS-binding activity of MFG-E8 was present in membrane vesicle fractions (density 1.05-1.13 g/ml), rather than milk fat globule fractions. The weaning-induced MFG-E8 might play an important role in the recognition and engulfment of apoptotic epithelial cells by the neighbouring phagocytic epithelial cells in involuting mammary glands. © 2006 Biochemical Society.

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  69. Hypoxic culture induces expression of sialin, a sialic acid transporter, and cancer-associated gangliosides containing non-human sialic acid on human cancer cells

    Yin J, Hashimoto A, Izawa M, Miyazaki K, Chen GY, Takematsu H, Kozutsumi Y, Suzuki A, Furuhata K, Cheng FL, Lin CH, Sato C, Kitajima K, Kannagi R

    CANCER RESEARCH   66 巻 ( 6 ) 頁: 2937 - 2945   2006年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Cancer Research  

    Tumor hypoxia figures heavily in malignant progression by altering the intracellular glucose metabolism and inducing angiogenic factor production, thus, selecting and expanding more aggressive cancer cell clones. Little is known, however, regarding hypoxia-induced antigenic changes in cancers. We investigated the expression of N-glycolyl sialic acid (NeuGc)-GM2, a cancer-associated ganglioside containing non-human sialic acid, NeuGc, in human cancers. Cancer tissues prepared from patients with colon cancers frequently expressed NeuGc-GM2, whereas it was virtually absent in nonmalignant colonic epithelia. Studies on cultured cancer cells indicated that the non-human sialic acid was incorporated from culture medium. Hypoxic culture markedly induced mRNA for a sialic acid transporter, sialin, and this accompanied enhanced incorporation of NeuGc as well as N-acetyl sialic acid. Transfection of cells with sialin gene conferred accelerated sialic acid transport and induced cell surface expression of NeuGc-GM2. We propose that the preferential expression of NeuGc-GM2 in cancers is closely associated with tumor hypoxia. Hypoxic culture of tumor cells induces expression of the sialic acid transporter, and enhances the incorporation of non-human sialic acid from the external milieu. A consequence of this is the acquisition of cancer-associated cell surface gangliosides, typically GM2, containing non-human sialic acid (NeuGc), which is not endogenously synthesized through CMP-N-acetyl sialic acid hydroxylase because humans lack the gene for the synthetic enzyme. As hypoxia is associated with diminished response to radiotherapy and chemotherapy, NeuGc-GM2 is a potential therapeutic target for hypoxic cancer cells. ©2006 American Association for Cancer Research.

    DOI: 10.1158/0008-5472.CAN-05-2615

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  70. AN N-TERMINAL 130 KDA FRAGMENT OF A FOURTH SEA URCHIN SPERM RECEPTOR FOR EGG JELLY MODULE PROTEIN, REJ4, IS SECRETED DURING ACROSOME REACTION(Developmental Biology,Abstracts of papers presented at the 76^<th> Annual Meeting of the Zoological Society of Japan) :

    MiyataShinji, SatoChihiro, ToriyamaMasaru, KitajamaKen

    Zoological science   22 巻 ( 12 ) 頁: 1456   2005年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Zoological Society of Japan  

    CiNii Research

  71. CAPACITATION-INDUCED CHANGES OF THE SURFACE DISTRIBUTION OF SIALOGLYCOTOPES ON PIG SPERM(Developmental Biology,Abstracts of papers presented at the 76^<th> Annual Meeting of the Zoological Society of Japan) :

    XueLian, MiyataShinji, SatoChihiro, KitajimaKen

    Zoological science   22 巻 ( 12 ) 頁: 1456   2005年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Zoological Society of Japan  

    CiNii Research

  72. An N-terminal 130 kDa fragment of a fourth sea urchin sperm receptor for egg jelly module protein, REJ4, is secreted during acrosome reaction

    Miyata Shinji, Sato Chihiro, Toriyama Masaru, Kitajama Ken

    ZOOLOGICAL SCIENCE   22 巻 ( 12 ) 頁: 1456 - 1456   2005年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  73. Capacitation-induced changes of the surface distribution of sialoglycotopes on pig sperm

    Xue Lian, Miyata Shinji, Sato Chihiro, Kitajima Ken

    ZOOLOGICAL SCIENCE   22 巻 ( 12 ) 頁: 1456 - 1456   2005年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  74. 5.糖鎖と発生、4)ポリシアル酸

    佐藤 ちひろ

    遺伝子医学(糖鎖と病気)MOOK 3     頁: 186 - 191   2005年

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    掲載種別:研究論文(学術雑誌)  

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  75. A MAJOR GANGLIOSIDE FROM HEMICENTROTUS PULCHERRIMUS SPERM SPECIFICALLY INTERACTS WITH PHOSPHOLIPIDS(Developmental Biology,Abstracts of papers presented at the 75^<th> Annual Meeting of the Zoological Society of Japan) :

    YamakawaNao, SatoChihiro, KitajimaKen

    Zoological science   21 巻 ( 12 ) 頁: 1292   2004年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Zoological Society of Japan  

    CiNii Research

  76. CELL GROWTH STIMULATING ACTIVITY OF THE PEPTIDES DERIVED FROM CORTICAL ALVEOLUS GLYCOPROTEINS OF FISH EGG (HYOSOPHORIN)(Developmental Biology,Abstracts of papers presented at the 75^<th> Annual Meeting of the Zoological Society of Japan) :

    MaedaEri, SatoChihiro, KitajimaKen

    Zoological science   21 巻 ( 12 ) 頁: 1292   2004年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Zoological Society of Japan  

    CiNii Research

  77. THE 130 KDA GLYCOPROTEIN IS SECRETED FROM SPERM DURING ACROSOME REACTION OF SEA URCHIN, HEMICENTROTUS PULCHERRIMUS(Developmental Biology,Abstracts of papers presented at the 75^<th> Annual Meeting of the Zoological Society of Japan) :

    MiyataShinji, SatoChihiro, ToriyamaMasaru, HirohashiNoritaka, VacquierVictor, KitajimaKen

    Zoological science   21 巻 ( 12 ) 頁: 1292   2004年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Zoological Society of Japan  

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  78. A major ganglioside from Hemicentrotus pulcherrimus sperm specifically interacts with phospholipids

    Yamakawa Nao, Sato Chihiro, Kitajima Ken

    ZOOLOGICAL SCIENCE   21 巻 ( 12 ) 頁: 1292 - 1292   2004年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  79. The 130 kDa glycoprotein is secreted from sperm during acrosome reaction of sea urchin, Hemicentrotus pulcherrimus

    Miyata Shinji, Sato Chihiro, Toriyama Masaru, Hirohashi Noritaka, Vacquier Victor, Kitajima Ken

    ZOOLOGICAL SCIENCE   21 巻 ( 12 ) 頁: 1292 - 1292   2004年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  80. A newly identified zona pellucida glycoprotein, ZPD, and dimeric ZP1 of chicken egg envelope are involved in sperm activation on sperm-egg interaction.

    Okumura H, Kohno Y, Iwata Y, Mori H, Aoki N, Sato C, Kitajima K, Nadano D, Matsuda T

    The Biochemical journal   384 巻 ( Pt 1 ) 頁: 191 - 9   2004年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical Journal  

    Fertilization begins with interaction between the sperm and the egg. The surface of the vertebrate oocyte is covered with the egg envelope, which is composed of ZP (zona pellucida) glycoproteins. We have identified two glycoproteins, ZP1/gp97 and ZPC/gp42, as the major components of the chicken egg envelope. In the present study, another 42 kDa protein, designated ZPD, has been found as a new major component of the chicken egg envelope. ZPD was specifically released from the egg envelope by ultrasonication treatment without urea. ZPD cDNA was cloned using a chicken granulosa cell cDNA pool. The deduced amino acid sequence showed that preproprotein of ZPD is composed of 418 amino acid residues with four potential N-glycosylation sites and includes a ZP domain, common in vertebrate ZP glycoproteins, and a transmembrane domain. ZPD belongs phylogenetically to a distinct group from known ZP glycoprotein subfamilies, ZPA, ZPB, and ZPC. In two-dimensional gel electrophoresis ZPD proteins were identified to be several isoforms with different pi values between 5 and 7. ZP1, ZPC and the newly identified ZPD were confirmed to be the major components of chicken egg envelope by MS of proteolytic digests of whole egg envelope. The in vitro incubation of chicken sperm with calcium ionophore A23187 induced sperm activation, resulting in the fragmentation and release of a 41 kDa PNA (peanut agglutinin)-positive glyco-protein and the decrease or loss of sperm PNA-stainability. The incubation with ZPD and dimeric ZP1, but not ZPC and monomeric ZPl, also induced the decrease or loss of sperm PNA-stainability, suggesting the in vitro sperm activation by these ZP components. Collectively, ZPD might bind loosely to egg envelope matrix and play a key role in the sperm activation on avian sperm-egg interaction.

    DOI: 10.1042/BJ20040299

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  81. Development of sensitive chemical and immunochemical methods for detecting sulfated sialic acids and their application to localization and quantitation studies of sea urchin sperm and eggs

    Yamakawa N, Maehashi E, Miyata S, Sato C, Furuhata K, Kitajima K

    GLYCOBIOLOGY   14 巻 ( 11 ) 頁: 1146 - 1146   2004年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  82. Effects of exogenously administered mannose and deaminoneuraminic acid (KDN) to mice or murine cultured cells on the metabolism of KDN

    Go S, Sato C, Kitajima K

    GLYCOBIOLOGY   14 巻 ( 11 ) 頁: 1166 - 1167   2004年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  83. Mouse heat shock protein 70 recognizes negatively charged glycolipids and phospholipids

    Harada Y, Sato C, Kitajima K

    GLYCOBIOLOGY   14 巻 ( 11 ) 頁: 1101 - 1102   2004年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  84. Occurrence and characterization of a novel sulfated alpha 2,9-linked polysialic acid-containing glycoprotein in sea urchin sperm flagellum

    Miyata S, Sato C, Kitajima K

    GLYCOBIOLOGY   14 巻 ( 11 ) 頁: 1146 - 1146   2004年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  85. Mouse T cell CD166 is a disialic acid-containing glycoprotein and involved in T cell activation

    Sato C, Nohara K, Matsuda T, Kitajima K

    GLYCOBIOLOGY   14 巻 ( 11 ) 頁: 1136 - 1136   2004年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  86. Specificity of human trans-sialidase as probed with gangliosides

    Nikonova EY, Tertov VV, Sato C, Kitajima K, Bovin NV

    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS   14 巻 ( 20 ) 頁: 5161 - 5164   2004年10月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Bioorganic and Medicinal Chemistry Letters  

    Human blood trans-sialidase able to form and split α2-8 disialic bond in gangliosides. © 2004 Elsevier Ltd. All rights reserved.

    DOI: 10.1016/j.bmcl.2004.07.058

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  87. 「シアル酸研究の新たな潮流」の特集にあたって

    SATO Chihiro

    Trends in glycoscience and glycotechnology   16 巻 ( 91 ) 頁: 291 - 292   2004年9月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

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  88. Preface for the special issue entitled "new waves in sialobioscience"

    Sato C.

    Trends in Glycoscience and Glycotechnology   16 巻 ( 91 ) 頁: 291 - 292   2004年9月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Trends in Glycoscience and Glycotechnology  

    DOI: 10.4052/tigg.16.291

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  89. Chain length diversity of sialic acids and its biological significance

    Sato C.

    Trends in Glycoscience and Glycotechnology   16 巻 ( 91 ) 頁: 331 - 344   2004年9月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Trends in Glycoscience and Glycotechnology  

    Sialic acids are commonly present as monosialyl residues at the non-reducing terminal end of glycoconjugates. In some cases, αc2→8 linked di/oligosialic acid chains with DP 2 or 3 sialic acid residues are common structural units of gangliosides, and involved in various biological processes, such as cell adhesion, cell differentiation, signal transduction, and surface expression of stage specific antigen. In contrast, little attention has been paid to the occurrence and functions of such short sialyl di/oligomers on glycoproteins, while polysialic acid (DP≥8) in embryonic NCAM has been extensively studied as a regulator of cell adhesion in neurogenesis. As analytical methods to detect di/oligosialic acid structures have been improved, several glycoproteins containing di/oligo/polysialic acid chains have been identified. It is thus hypothesized that these di/oligosialic acid residues on glycoproteins may have similar important functions in common with those proposed for the gangliosides or may have new functions. Currently, several studies showing the importance of di/oligosialic acid-containing glycoproteins have emerged. In this review, recent advances in such studies of di/ oligosialic acid residues on glycoproteins, including analytical methods, occurrence, biosynthetic pathways, and functions, are described.

    DOI: 10.4052/tigg.16.331

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  90. Developmental Expression of a Sialyltransferase Responsible for Sialylation of Cortical Alveolus Glycoprotein during Oogenesis in Rainbow Trout (Oncorhynchus mykiss)

    ASAHINA Shinji, SATO Chihiro, KITAJIMA Ken

    Journal of Biochemistry   136 巻 ( 2 ) 頁: 189 - 198   2004年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  91. Developmental expression of a sialyltransferase responsible for sialylation of cortical alveolus glycoprotein during oogenesis in rainbow trout (Oncorhynchus mykiss).

    Asahina S, Sato C, Kitajima K

    Journal of biochemistry   136 巻 ( 2 ) 頁: 189 - 98   2004年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biochemistry  

    Polysialoglycoprotein (PSGP) is a major cortical alveolus glycoprotein of rainbow trout eggs that is characterized by the attachment of a polysialic acid structure to its O-glycan chains. It has been demonstrated that the polysialic acid structure is synthesized by at least three sialyltransferases mostly localized in cortical alveoli. Here we have cloned a cDNA encoding the sialyltransferase, designated rtST6GalNAc, responsible for the transfer of the first sialic acid residue onto the O-glycan chain of PSGP. This enzyme belongs to the vertebrate ST6GalNAc II family, and is strongly expressed in ovaries. Of those O-glycoproteins tested as substrates, asialo-PSGP is the best substrate. These results indicate that rtST6GalNAc is the enzyme responsible for the sialylation of PSGP during oogenesis. Furthermore, the rtST6GalNAc mRNA is expressed throughout oogenesis, is down-regulated at the late yolk vesicle stage (May), and then up-regulated during vitellogenesis (until August). This developmental profile is highly similar to that of STL2, a cortical alveolus lectin, while it is quite different from that of PSGP, which is extensively expressed at the yolk vesicle stage and down-regulated at later stages. Thus, not all cortical alveolus components are transcribed concomitantly. This is the first description of a developmental change in the transcription of a glycosyltransferase during oogenesis.

    DOI: 10.1093/jb/mvh106

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  92. Alpha-C-mannosyltryptophan is not recognized by conventional mannose-binding lectins.

    Nishikawa T, Kajii S, Sato C, Yasukawa Z, Kitajima K, Isobe M

    Bioorganic & medicinal chemistry   12 巻 ( 9 ) 頁: 2343 - 8   2004年5月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Bioorganic and Medicinal Chemistry  

    α-C-Mannosyltryptophan (C-Man-Trp) is a novel, naturally occurring C-linked carbohydrate-protein linkage first found in 1994 from human ribonuclease 2. Since then, a number of C-Man-Trp residue have been found from several important proteins such as interleukin 12β, components of complement system, thrombospondin-1, and erythropoietin receptor, however, the biological functions have remained unknown even though its biosynthetic pathway has been revealed. In order to find a clue as to the biological functions, we examined the affinity of C-Man-Trp with conventional mannose lectin such as concanavarin A (Con A) and mannose-binding lectin (MBL). The affinity of C-Man-Trp with Con A, a typical mannose-binding lectin from plant was examined using a Con A-Sepharose column. Unlike p-nitrophenyl-α-O-Man, C-Man-Trp was not retained on the column. MBL-C, a major mannose-binding lectin purified from mouse serum, did not bind with N-biotinylated C-Man-Trp, judging from ELISA based assay. These results imply that C-Man-Trp may be recognized with the other specific proteins associated with its unknown biological functions. © 2004 Elsevier Ltd.

    DOI: 10.1016/j.bmc.2004.02.009

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  93. ジシアル酸・オリゴシアル酸・ポリシアル酸の生物学的機能

    佐藤 ちひろ

    Functional Glycomics 3     頁: 40 - 47   2004年

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    掲載種別:研究論文(学術雑誌)  

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  94. FORMATION OF MEMBRANE MICRODOMAINS IS SIGNIFICANT IN DEVELOPING EMBRYOS OF MEDAKA(Developmental Biology,Abstracts of papers presented at the 74^<th> Annual Meeting of the Zoological Society of Japan) :

    AdachiTomoko, SatoChihiro, KitajimaKen

    Zoological science   20 巻 ( 12 ) 頁: 1570   2003年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Zoological Society of Japan  

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  95. [Frequent occurrence and biological significance of degree of polymerization in sialic acid]. 査読有り

    Sato C

    Seikagaku. The Journal of Japanese Biochemical Society   75 巻 ( 12 ) 頁: 1526 - 30   2003年12月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

    PubMed

  96. FUNCTIONS OF THE COMMON GLYCOTOPES OF GLYCOLIPIDS AND GLYCOPROTEINS IN THE MEMBRANE MICRODOMAIN OF SEA URCHIN SPERM(Developmental Biology)(Proceedings of the Seventy-Third Annual Meeting of the Zoological Society of Japan) :

    MiyataShinji, MaehashiEri, OhtaKaoru, SatoChihiro, MatsudaTsukasa, KitajimaKen

    Zoological science   19 巻 ( 12 ) 頁: 1443   2002年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Zoological Society of Japan  

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  97. Neuronal differentiation-dependent expression of the disialic acid epitope on CD166 and its involvement in neurite formation in Neuro2A cells.

    Sato C, Matsuda T, Kitajima K

    The Journal of biological chemistry   277 巻 ( 47 ) 頁: 45299 - 305   2002年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    We previously demonstrated that α2,8-linked disialic acid (diSia) residues occur in several glycoproteins of mammalian brains (Sato, C., Fukuoka, H., Ohta, K., Matsuda, T., Koshino, R., Kobayashi, K., Troy, F. A., II, and Kitajima, K. (2000) J. Biol. Chem. 275, 15422-15431). The role of the diSia epitope on these glycoproteins is not known, whereas the importance of the diSia epitope on glycolipids is well documented in neurite formation. In this study, we demonstrated that the diSia epitope (Neu5Acα2 → 8Neu5Acα2 → 3Gal) on glycoproteins, but not on glycolipids, is involved in neurite formation in a mouse neuroblastoma cell line, Neuro2A, based on the following lines of evidence. First, the amount of diSia epitope on glycoproteins increased during retinoic acid-induced neurite formation. Second, retinoic acid treatment primarily increased the diSia epitope on a 100-kDa glycoprotein. We identified this protein as CD166 (SC1), an immunoglobulin superfamily cell adhesion molecule involved in neurite extension. Third, a monoclonal antibody against the diSia epitope specifically inhibited neurite formation. We also demonstrated that α2,8-sialyltransferase III mRNA expression increased 1.7-fold after the induction of neurite formation, suggesting that α2,8-sialyltransferase III is responsible for formation of the diSia epitope on CD166.

    DOI: 10.1074/jbc.M206046200

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  98. ジ・オリゴシアル酸構造の生物学的機能

    佐藤 ちひろ, 北島 健

      6 巻   頁: A4J   2002年6月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:生化学工業株式会社  

    DOI: 10.32285/glycoforum.06a4j

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  99. Function of Di/oligosialic Acid Structure

    Sato Chihiro, Kitajima Ken

    Glycoforum   6 巻   頁: A4   2002年6月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:SEIKAGAKU CORPORATION  

    DOI: 10.32285/glycoforum.06a4

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  100. Occurrence of Oligosialic Acids on Integrin α<inf>5</inf> Subunit and Their Involvement in Cell Adhesion to Fibronectin

    Nadanaka S., Sato C., Kitajima K., Katagiri K., Irie S., Yamagata T.

    Journal of Biological Chemistry   276 巻 ( 36 ) 頁: 33657 - 33664   2001年9月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    Integrin α5β1, a major fibronectin receptor, functions in a wide variety of biological phenomena. We have found that α2-8-linked oligosialic acids with 5 ≤ degree of polymerization (DP) ≤ 7 occur on integrin α5 subunit of the human melanoma cell line G361. The integrin α5 subunit immunoprecipitated with anti-integrin α5 antibody reacted with the monoclonal antibody 12E3, which recognizes oligo/polysialic acid with DP ≥ 5 but not with the polyclonal antibody H.46 recognizing oligo/polysialic acid with DP ≥ 8. The occurrence of oligosialic acids was further demonstrated by fluorometric C7/C9 analysis on the immunopurified integrin α5 subunit. Oligosialic acids were also found in the α5 subunit of several other human cells such as foreskin fibroblast and chronic erythroleukemia K562 cells. These results suggest the ubiquitous modification with unique oligosialic acids occurs on the α 5 subunit of integrin α5β1. The adhesion of human melanoma G361 cells to fibronectin was mainly mediated by integrin α5β1. Treatment of cells with sialidase from Arthrobacter ureafaciens cleaving α2-3-, α2-6-, and α2-8-linked sialic acids inhibited adhesion to fibronectin. On the other hand, N-acetylneuraminidase II, which cleaves α2-3 and α2-6 but not α2-8 linkages, showed no inhibitory activity. After the loss of oligosialic acids, integrin α5β1 failed to bind to fibronectin-conjugated Sepharose, indicating that the oligosialic acid on the α5 subunit of integrin α5β 1 plays important roles in cell adhesion to fibronectin.

    DOI: 10.1074/jbc.M011100200

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  101. Identification and Adipocyte Differentiation-dependent Expression of the Unique Disialic Acid Residue in an Adipose Tissue-specific Glycoprotein, Adipo Q

    Sato C., Yasukawa Z., Honda N., Matsuda T., Kitajima K.

    Journal of Biological Chemistry   276 巻 ( 31 ) 頁: 28849 - 28856   2001年8月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    Recently, we have shown that α2,8-linked disialic acid (diSia) residue occurs in glycoproteins more frequently than ever recognized (Sato, C., Fukuoka, H., Ohta, K., Matsuda, T., Koshino, R., Kobayashi K., Troy, F. A., II, and Kitajima, K. (2000) J. Biol. Chem. 275, 15422-15431). In the course of identification of the diSia-containing glycoproteins in mammals, the 30-kDa glycoprotein was found in bovine serum. The 30-kDa glycoprotein was shown to be the bovine adipo Q, an adipocyte-specific protein, based on the partial amino acid sequences and the immuno-cross-reactivity with the recombinant mouse adipo Q. The bovine adipo Q was shown to have no N-linked but O-linked glycan(s) containing the diSia epitope, Neu5Acα2→8Neu5Acα2→3Gal. Furthermore, the diSia epitope was also found in the mouse adipo Q in serum as well as in the 3T3-L1 cells that are fully differentiated into adipocytes. Notably, among the known α2,8-sialyltransferases, only the α2,8-sialyltransferase III mRNA was detected in the 3T3-L1 cells at any stages of differentiation, and the recombinant α2,8-sialyltransferase III could sialylate the purified bovine adipo Q. Thus, this study clearly provides the new findings that adipo Q is the diSia-containing glycoprotein and a physiological substrate of α2,8-sialyltransferase III, whose substrates have not been identified so far.

    DOI: 10.1074/jbc.M104148200

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  102. 昆虫におけるシアル酸,その存在と意義

    佐藤 ちひろ

    Trends in Glycoscience and Glycotechnology   13 巻 ( 73 ) 頁: 507 - 517   2001年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:FCCA(Forum: Carbohydrates Coming of Age)  

    数種の昆虫の発生途上にシアル酸、主に、<i>N</i>-アセチルノイラミン酸が見出されてきている。我々はレクチンや抗体、単糖の様々な精製および分析法を用いることによって、ショウジョウバエ (<i>Drosophila melanogaster</i>) の神経発達領域およびセミ(<i>Philaenus spumarius</i>) のマルピーギ管にポリシアル酸を検出した。これらの昆虫の成体にシアル酸は検出されなかった。シアル酸の発現は <i>in vivo</i> では明らかであるが、多くの昆虫培養細胞系ではその存在が明らかにされていない。また、バキュロウイルスの発現系を用いて哺乳動物型の組換え糖タンパク質 (複合型シアリル化<i>N</i>-型糖鎖をもつもの)を生産することは利点が多くあるため、培養細胞におけるシアル酸の生合成機構の解明が生物工学的な観点から重要視されてきている。それらの研究によって明らかになったことは、糖鎖の改変は昆虫細胞に糖転移酵素群を発現させることによってのみ可能であることである。すなわちシアル酸の生合成に関わる酵素をコードするいくつかの外来遺伝子を導入しなくてはならない。さらに、昆虫細胞に関する研究によって、シアル酸は動物界の新口動物に限られているのではなく、昆虫のような原口動物にも存在することが明らかになった。このことはシアル酸の進化に対して新しい見解を投ずるものである。

    DOI: 10.4052/tigg.13.507

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  103. Co-localization of receptor and transducer proteins in the glycosphingolipid-enriched, low density, detergent-insoluble membrane fraction of sea urchin sperm

    Ohta K., Sato C., Matsuda T., Toriyama M., Vacquier V., Lennarz W., Kitajima K.

    Glycoconjugate Journal   17 巻 ( 3-4 ) 頁: 205 - 214   2000年12月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycoconjugate Journal  

    The low density, detergent-insoluble membrane fraction (LD-DIM), where gangliosides are likely to be highly enriched, was prepared from sperm of two sea urchin species, Hemicentrotus pulcherrimus and Strongylocentrotus purpuratus. Immunoblotting showed the presence in the LD-DIM of two receptors for egg ligands, a glycosylphosphatidylinositol (GPI)-anchored protein, and four proteins which may be involved in signal transduction. Co-immunoprecipitation revealed that at least three proteins, the speract receptor, the 63kDa GPI-anchored protein and the α subunit of a heterotrimeric Gs protein, are localized in the LD-DIM. This suggests that the LD-DIM fraction may be a membrane microdomain for speract-speract receptor interaction, as well as the subsequent signal transduction pathway involved in induction of sperm respiration, motility and possibly the acrosome reaction.

    DOI: 10.1023/A:1026589223811

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  104. Frequent occurrence of pre-existing α2→8-linked disialic and oligosialic acids with chain lengths up to 7 Sia residues in mammalian brain glycoproteins. Prevalence revealed by highly sensitive chemical methods and anti-di-, oligo-, and poly-Sia antibodies specific for defined chain lengths

    Sato C., Fukuoka H., Ohta K., Matsuda T., Koshino R., Kobayashi K., Troy F.A., Kitajima K.

    Journal of Biological Chemistry   275 巻 ( 20 ) 頁: 15422 - 15431   2000年5月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    The pre-existence of α2→8-linked disialic acid (di-Sia) and oligosialic acid (oligo-Sia) structures with up to 7 Sia residues was shown to occur on a large number of brain glycoproteins, including neural cell adhesion molecules (N-CAMs), by two highly sensitive chemical methods (Sato, C., Inoue, S., Matsuda, T., and Kitajima, K. (1998) Anal. Biochem. 261, 191- 197; Sato, C., Inoue, S., Matsuda, T., and Kitajima, K. (1999) Anal Biochem. 266, 102-109). This unexpected finding was also confirmed using a newly developed antibody prepared using a copolymer of α2→8-linked N- acetylneuraminyl p-vinylbenzylamide and acrylamide as an immunogen and known antibodies whose immunospecificities were determined to be di- and oligo-Sia residues with defined chain lengths. The major significance of the new finding that di- and oligo-Sia chains exist on a large number of brain glycoproteins is 2-fold. First, it reveals a surprising diversity in the number and M(r) of proteins distinct from N-CAM that are covalently modified by these short sialyl glycotopes. Second, it suggests that synthesis of di- and/or oligo-Sia units may be catalyzed by α2→8-sialyltransferase(s) that are distinct from the known polysialyltransferases, STX and PST, which are partially responsible for polysialylation of N-CAM.

    DOI: 10.1074/jbc.275.20.15422

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  105. Lipid raft on gametic cells as a functional domain for sperm-egg interaction coupled with signal transduction

    Ohta K., Sato C., Matsuda T., Toriyama M., Vacquier V.D., Hirohashi N., Lennarz W.J., Kitajima K.

    Zygote   8 巻 ( SUPPL. ) 頁: .   2000年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Zygote  

    DOI: 10.1017/s0967199400130321

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  106. O‐アセチル化シアル酸  その検出,生物学的意義,および病気における変化

    佐藤 ちひろ

    Trends in Glycoscience and Glycotechnology   12 巻 ( 63 ) 頁: 17 - 33   2000年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:FCCA(Forum: Carbohydrates Coming of Age)  

    シアル酸はカルボン酸をもつ酸性9炭糖であり、一般に、細胞膜局在あるいは分泌性の複合糖質の糖鎖の最も外側に位置している。この配位は、多くの細胞間および分子間相互作用の制御に関与しやすい点で好都合である。シアル酸は構造多様性をもつが、中でも最も多く見出されるのはC-<sub>4、7、9</sub>位の<i>O</i>-アセチル化体である。<i>O</i>-アセチル化シアル酸 (<i>O</i>-AcSA) における構造多様性は、それを担っている糖鎖の結合様式、<i>O</i>-アセチル化される炭素の位置、および結合している複合糖質の性状に起因する。分析手法が改善されてきたことによって、いくつかの病気における<i>O</i>-AcSA誘導体の同定が可能になったことから、興味の中心はこの修飾反応の生物学的重要性の理解へと方向変換してきた。この総説では、様々な病理生理学的状態に伴って変化する<i>O</i>-アセチル化体の検出法やそれらの生物学的関連性に関する最新の情報を扱っている。特に、9-<i>O</i>-アセチル化シアル酸含有複合糖質 (9-<i>O</i>AcSA) がその病気の診断マーカーとして有用である二つの全く異なる病気である、急性リンパ球性白血病 (ALL) と内臓リーシュマニア症 (VL) に注目している。

    DOI: 10.4052/tigg.12.17

    CiNii Research

  107. Lipid raft on gametic cells as a functional domain for sperm-egg interaction coupled with signal transduction

    Ohta K, Sato C, Matsuda T, Toriyama M, Vacquier VD, Hirohashi N, Lennarz WJ, Kitajima K

    ZYGOTE   8 巻   頁: S63 - S63   2000年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  108. Lipid raft on gametic cells as a functional domain for sperm-egg interaction coupled with signal transduction.

    Ohta K, Sato C, Matsuda T, Toriyama M, Vacquier VD, Hirohashi N, Lennarz WJ, Kitajima K

    Zygote (Cambridge, England)   8 Suppl 1 巻   頁: S63   2000年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    PubMed

  109. Glycobiology of Di- and Oligosialyl Glycotopes

    Sato C., Kitajima K.

    Trends in Glycoscience and Glycotechnology   11 巻 ( 62 ) 頁: 371 - 390   1999年11月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Trends in Glycoscience and Glycotechnology  

    α2→8-Linked di- and oligosialic acid (diSia and oligoSia) chains with DP 2,3 Sia residues are known to be common structural units of gangliosides, and to be involved in various biological processes, such as cell adhesion, cell differentiation, signal transduction, and surface expression of stage specific antigen. In contrast, little attention has been paid to the occurrence and functions of such short sialyl oligomers on glycoproteins. However, it has recently been shown that glycoproteins containing di- and oligoSia groups occur in nature more frequently than was ever recognized, as analytical methods to detect di- and oligoSia structures have improved. It is thus hypothesized that these di- and oligoSia moieties on glycoproteins may have similar important functions in common with those proposed for the gangliosides. In this review, we describe the recent advances in the study of di- and oligoSia residues on glycoproteins, including analytical methods, occurrence, functions, and biosynthetic pathways.

    DOI: 10.4052/tigg.11.371

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  110. Cholesterol-dependent localization of NAP-22 on a neuronal membrane microdomain (Raft)

    Maekawa S., Sato C., Kitajima K., Funatsu N., Kumanogoh H., Sokawa Y.

    Journal of Biological Chemistry   274 巻 ( 30 ) 頁: 21369 - 21374   1999年7月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    A membrane microdomain called raft has been under extensive study since the assembly of various signal-transducing molecules into this region has been envisaged. This domain is isolated as a low buoyant membrane fraction after the extraction with a nonionic detergent such as Triton X-100. The characteristic low density of this fraction is ascribed to the enrichment of several lipids including cholesterol. To clear the molecular mechanism of raft formation, several extraction methods were applied to solubilize raft components. Cholesterol extraction using methyl-β-cyclodextrin was found to be effective to solubilize NAP-22, a neuron-enriched Ca2+-dependent calmodulin-binding protein as well as one of the main protein components of brain raft. Purified NAP-22 bound to the liposomes that were made from phosphatidylcholine and cholesterol. This binding was dependent on the amount of cholesterol in liposomes. Calmodulin inhibited this binding in a dose- dependent manner. These results suggest that the presence of a calcium- dependent regulatory mechanism works on the assembly of raft within the neuron.

    DOI: 10.1074/jbc.274.30.21369

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  111. Isolation and characterization of low density detergent-insoluble membrane (LD-DIM) fraction from sea urchin sperm

    Ohta K., Sato C., Matsuda T., Toriyama M., Lennarz W., Kitajima K.

    Biochemical and Biophysical Research Communications   258 巻 ( 3 ) 頁: 616 - 623   1999年5月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical and Biophysical Research Communications  

    The low density detergent-insoluble membrane (LD-DIM) fraction was obtained by a sucrose-density gradient centrifugation from sperm of three sea urchin species, Hemicentrotus pulcherrimus, Strongylocentrotus purpuratus, and Anthocidaris crassispina. These LD-DIM preparations were characterized by enriched glycosphingolipids (GSL) including gangliosides and sulfatide (SLF), having more than 50% of the total amount of GSL present in these sperm. Interestingly, a minor component of H. pulcherrimus sperm (HO3S→8Neu5Acα2→8Neu5Acα2→6Glcβ1→Cer) was shown to be even more enriched in the LD-DIM as revealed by using monoclonal antibody (mAb.3G9) specific to this ganglioside. In addition to the GSL, phosphatidylserine (PS) and diacylglycerol (DG) were enriched in the LD-DIM. On the other hand, cholesterol (CL) and sphingomyelin (SM) were not so enriched, which contrasted with the LD-DIM from Madin-Darby canine kidney (MDCK) cells, where CL and SM were reported to be abundant. Because mammalian somatic cell-derived DIMs have been proposed to be associated with functional signal transduction, it seems possible that the ganglioside-enriched LD-DIM in sea urchin sperm can participate in binding to eggs and the subsequent egg activation process. To our knowledge this is the first chemical characterization of the LD-DIM fraction of a gametic cell.

    DOI: 10.1006/bbrc.1999.0686

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  112. A 42-kDa glycoprotein from chicken egg-envelope, an avian homolog of the ZPC family glycoproteins in mammalian zona pellucida. Its first identification, cDNA cloning and granulosa cell-specific expression

    Takeuchi Y., Nishimura K., Aoki N., Adachi T., Sato C., Kitajima K., Matsuda T.

    European Journal of Biochemistry   260 巻 ( 3 ) 頁: 736 - 742   1999年3月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:European Journal of Biochemistry  

    A glycoprotein with molecular mass of 42 kDa was identified as the major component of the chicken egg-envelope, the filamentous, extracellular matrix known as the perivitelline layer. By using a DNA probe amplified with degenerative primers derived from the protein's partial amino acid sequences, a cDNA clone encoding the egg-envelope 42-kDa glycoprotein (gp42) was isolated from a hen's ovary cDNA library. The gp42 open reading frame encoded 435 amino acid residues, including a putative signal peptide of 20 amino acids. The deduced amino acid sequence of gp42 showed significant similarity to egg-envelope glycoproteins of the ZPC family of several other vertebrate species, including human ZP3, mouse ZP3, Xenopus laevis gp43 and medaka (Oryzias latipes) ZI3 (LS-F), which play important roles for sperm-egg interaction. A single N-glycosylation site present in chicken gp42 is conserved among all five of these proteins: carbohydrate analysis of gp42 revealed the presence of a complex type glycan chain at this site. N-terminal sequence analysis of the mature polypeptide suggests that C-terminal processing of the pro-protein occurs during synthesis and secretion. The 1.4- kb gp42 transcript was detected only in follicles, and was found to be accumulated in granulosa cells in a manner dependent on ovarian follicular development. Furthermore, a metabolically radio-labeled gp42 was immunoprecipitated from both cell lysate and culture supernatant of the granulosa cells with specific anti-gp42 antibody, suggesting granulosa cell- specific synthesis and secretion of the glycoprotein.

    DOI: 10.1046/j.1432-1327.1999.00203.x

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  113. Fluorescent-assisted detection of oligosialyl units in glycoconjugates

    Sato C., Inoue S., Matsuda T., Kitajima K.

    Analytical Biochemistry   266 巻 ( 1 ) 頁: 102 - 109   1999年1月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Analytical Biochemistry  

    A highly sensitive chemical method to detect various types of oligo/polysialic acid (oligo/polySia) units in glycoconjugates, i.e., α2 → 8-linked homooligo/polySia [N-acetylneuraminic acid (Neu5Ac), N- glcolylneuraminic acid (Neu5Gc), or 2-keto-3-deoxy-D-glycero-D-galacto- nononic acid], α2 → 8-linked heterodimers of Neu5Ac and Neu5Gc, α2 → 9- linked homooligo/polyNeu5Ac, and α2 → 5-O(glycolyl)-linked homooligo/polyNeu5Gc, was developed with an α-keto acid-reactive fluorescent labeling reagent, 1,2-diamino-4,5-methylenedioxybenzene (DMB). Fluorescent labeled di- or oligoSia was separated and quantitated by fluorometric anion- exchange high-performance liquid chromatography (HPLC). As little as 13 fmol of Neu5Acα2 → 8Neu5Ac was detectable by this method. When α2 → 8-linked oligo/polyNeu5Ac with on average eight Neu5Ac residues was labeled with DMB, DMB derivatives of oligomers with only lower degrees of polymerization of 2 to 7, were detected, due to concomitant partial depolymerization of oligo/polySia chain with the derivatization. For glycoproteins and glycolipids, mild acid hydrolysis was performed to release oligoSia prior to DMB derivatization. The mild acid hydrolysis/fluorometric HPLC method was also applicable to glycoprotein samples blotted on the membrane.

    DOI: 10.1006/abio.1998.2921

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  114. Development of a highly sensitive chemical method for detecting α2→8- linked oligo/polysialic acid residues in glycoproteins blotted on the membrane

    Sato C., Inoue S., Matsuda T., Kitajima K.

    Analytical Biochemistry   261 巻 ( 2 ) 頁: 191 - 197   1998年8月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Analytical Biochemistry  

    A highly sensitive chemical method for detecting α2→8-linked oligo/polysialic acid (oligo/polySia) chains was developed, including (i) periodate oxidation, reduction with sodium borohydride, and subsequent acid hydrolysis, giving rise to C7 analogues and intact C9 compounds from nonreducing terminal and internal sialic acid residues, respectively; (ii) fluorescent labeling of these C7 and C9 compounds with 1,2-diamino-4,5- methylenedioxybenzene (DMB); and (iii) quantitation of these DMB derivatives on fluorometric high-performance liquid chromatography. As little as 1 ng of internal sialic acid residues of oligo/polySia chains, the existence of which indicates the presence of oligo/polySia structure, was detectable by this method. This fluorometric C7/C9 analysis was successfully applied to glycoproteins blotted onto a slit of polyvinylidene fluoride membranes and suggested the presence of some novel oligoSia-containing glycoproteins in pig embryonic brains.

    DOI: 10.1006/abio.1998.2718

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  115. Identification of oligo-N-glycolylneuraminic acid residues in mammal- derived glycoproteins by a newly developed immunochemical reagent and biochemical methods

    Sato C., Kitajima K., Inoue S., Inoue Y.

    Journal of Biological Chemistry   273 巻 ( 5 ) 頁: 2575 - 2582   1998年1月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    The occurrence of the α2→8-linked oligomeric form of N- glycolylneuraminic acid (oligo-Neu5Gc) residues in mammalian glycoproteins was unequivocally demonstrated using a newly developed anti-oligo/poly- Neu5Gc monoclonal antibody as well as by chemical and biochemical methods. First, the antibody, designated mAb.2-4B, which specifically recognized oligo/poly-Neu5Gc with a degree of polymerization of >2, was developed by establishing a hybridoma cell line from P3U1 myeloma cells fused with splenocytes from an MRL autoimmune mouse immunized with dipalmitoylphosphatidylethanolamine-conjugated oligo/poly-Neu5Gc. Second, oligo-Neu5Gc was shown to occur in glycoproteins derived from pig spleen by Western blot analysis using mAb.2-4B, which was also confirmed by fluorometric high performance liquid chromatographic analysis of the product of periodate oxidation/reduction/acid hydrolysis of the purified glycopeptide fractions and by TLC and 600-MHz 1H NMR spectroscopic analysis of their mild acid hydrolysates. Finally, the ubiquitous occurrence of oligo-Neu5Gc chains as glycoproteinaceous components in Wistar rat tissue was immunochemically indicated. This is the first example demonstrating the diversity in oligo/poly-Sia structure in mammalian glycoproteins, where only poly-N- acetylneuraminic acid is known to occur. Such diversity in oligo/poly-Sia structure also implicates a diverged array of biological functions of this glycan unit in glycoproteins.

    DOI: 10.1074/jbc.273.5.2575

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  116. Occurrence of terminal α2 → 8-linked disialylated poly-N-acetyllactosamine chains with Le(X) and I antigenic glycotopes in tetraantennary arms of an N-linked glycoprotein isolated from rainbow trout ovarian fluid

    Funakoshi Y., Taguchi T., Sato C., Kitajima K., Inoue S., Morris H.R., Dell A., Inoue Y.

    Glycobiology   7 巻 ( 2 ) 頁: 195 - 205   1997年3月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    The Pronase digestion of a 54K glycoprotein present in ovarian fluid of rainbow trout yielded a major glycopeptide. Carbohydrate compositional analysis revealed that this glycopeptide was likely to possess a single large N-glycan chain having low molecular weight oligomers of N-acetylneuraminic acid (oligoNeu5Ac). Structural studies of this glycopeptide revealed novel α2 → 8-linked disialylated poly-N-acetyllactosamine chains with Le(X) and I antigenic determinants on the N-linked tetraantennary core glycan. In our recent studies (Kitazume, S., Kitajima, K., Inoue, S., Inoue, Y. and Troy, F.A. (1994) J. Biol. Chem. 269, 10330-10340) we presented evidence that synthesis of α2 → 8-linked polysialic acid (polySia) chains is a two-step process in which chain initiation is catalyzed by an α2 → 8-sialyltransferase (α2 → 8-ST; initiase) that catalyzes synthesis of the first Sia α2 → 8-linkage, forming the disialic acid (diSia) unit, Siaα2 → 8-Siaα2 → 6-Gal-.Chain polymerization is then postulated to be catalyzed by a second enzyme, an α2 → 8-polyST ('polymerase') that converts the diSia units to polySia chains. The present structural studies leading to the discovery of α2 → 8-linked disialylated units that terminate poly-N-acetyllactosamine chains in an N-linked glycoprotein is further evidence in support of our hypothesis that more than one sialyltransferase activity is required for polySia chain synthesis and polymerization.

    DOI: 10.1093/glycob/7.2.195

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  117. Implication of N-glycolylneuraminic acid in regulation of cell adhesiveness of C2C12 myoblast cells during differentiation into myotube cells. 国際誌

    Go S, Sato C, Hane M, Go S, Kitajima K

    Glycoconjugate journal   39 巻 ( 5 ) 頁: 619 - 631   2022年10月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycoconjugate Journal  

    A transition of sialic acid (Sia) species on GM3 ganglioside from N-acetylneuraminic acid (Neu5Ac) to N-glycolylneuraminic acid (Neu5Gc) takes place in mouse C2C12 myoblast cells during their differentiation into myotube cells. However, the meaning of this Sia transition remains unclear. This study thus aims to gain a functional insight into this phenomenon. The following lines of evidence show that the increased de novo synthesis of Neu5Gc residues in differentiating myoblast cells promotes adhesiveness of the cells, which is beneficial for promotion of differentiation. First, the Sia transition occurred even in the C2C12 cells cultured in serum-free medium, indicating that it happens through de novo synthesis of Neu5Gc. Second, GM3(Neu5Gc) was localized in myoblast cells, but not in myotube cells, and related to expression of the CMP-Neu5Ac hydroxylase (CMAH) gene. Notably, expression of CMAH precedes myotube formation not only in differentiating C2C12 cells, but also in mouse developing embryos. Since the myoblast cells were attached on the dish surface more strongly than the myotube cells, expression of GM3(Neu5Gc) may be related to the surface attachment of the myoblast cells. Third, exogenous Neu5Gc, but not Neu5Ac, promoted differentiation of C2C12 cells, thus increasing the number of cells committed to fuse with each other. Fourth, the CMAH-transfected C2C12 cells were attached on the gelatin-coated surface much more rapidly than the mock-cells, suggesting that the expression of CMAH promotes cell adhesiveness through the expression of Neu5Gc.

    DOI: 10.1007/s10719-022-10049-9

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  118. The α2,8-sialyltransferase 6 (St8sia6) localizes in the ER and enhances the anchorage-independent cell growth in cancer. 国際誌

    Hatanaka R, Araki E, Hane M, Go S, Wu D, Kitajima K, Sato C

    Biochemical and biophysical research communications   608 巻   頁: 52 - 58   2022年6月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical and Biophysical Research Communications  

    Sialylation, the final stage of post-translational modification of proteins, is achieved in the Golgi apparatus and is related to the malignant phenotype of cancer. Disialylation of ganglioside (GD3) by St8sia1 and polysialylation by St8sia2 and 4 have been shown to be related to malignant phenotypes; however, di/oligosialylation by St8sia6 is still unknown. In this study, we analyzed the malignant phenotype of St8sia6 and found that upregulation of St8sia6 in melanoma B16 cells increased anchorage-independent cell growth, which was not due to sialic acid cleavage by a sialidase. Moreover, unlike other sialyltransferases, St8sia6 localized to the endoplasmic reticulum (ER). We found that the localization to the Golgi apparatus could be regulated by swapping experiments using St8sia2; however, the malignant phenotype did not change. These data demonstrate that the enhancement of anchorage-independent cell growth by St8sia6 is not due to its localization of ER, but is due to the expression of the protein itself.

    DOI: 10.1016/j.bbrc.2022.03.146

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  119. Comprehensive Analysis of Oligo/Polysialylglycoconjugates in Cancer Cell Lines. 国際誌

    Hane M, Kitajima K, Sato C

    International journal of molecular sciences   23 巻 ( 10 )   2022年5月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:International Journal of Molecular Sciences  

    In cancer cells, cell-surface sialylation is altered, including a change in oligo/polysialic acid (oligo/polySia) structures. Since they are unique and rarely expressed in normal cells, oligo/polySia structures may serve as promising novel biomarkers and targets for therapies. For the diagnosis and treatment of the disease, a precise understanding of the oligo/polySia structures in cancer cells is necessary. In this study, flow cytometric analysis and gene expression datasets were obtained from sixteen different cancer cell lines. These datasets demonstrated the ability to predict glycan structures and their sialylation status. Our results also revealed that sialylation patterns are unique to each cancer cell line. Thus, we can suggest promising combinations of antibody and cancer cell for glycan prediction. However, the precise prediction of minor glycans need to be further explored.

    DOI: 10.3390/ijms23105569

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  120. Polysialylation in a DISC1 Mutant Mouse. 国際誌

    Takahashi Y, Abe C, Hane M, Wu D, Kitajima K, Sato C

    International journal of molecular sciences   23 巻 ( 9 )   2022年5月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:International Journal of Molecular Sciences  

    Schizophrenia is a serious psychiatric disorder that affects the social life of patients. Psychiatric disorders are caused by a complex combination of genetic (G) and environmental (E) factors. Polysialylation represents a unique posttranslational modification of a protein, and such changes in neural cell adhesion molecules (NCAMs) have been reported in postmortem brains from patients with psychiatric disorders. To understand the G × E effect on polysialylated NCAM expression, in this study, we performed precise measurements of polySia and NCAM using a disrupted-in-schizophrenia 1 (DISC1)-mutant mouse (G), a mouse model of schizophrenia, under acute stress conditions (E). This is the first study to reveal a lower number and smaller length of polySia in the suprachiasmatic nucleus of DISC1 mutants relative to those in wild-type (WT) mice. In addition, an analysis of polySia and NCAM responses to acute stress in five brain regions (olfactory bulb, prefrontal cortex, suprachiasmatic nucleus, amygdala, and hippocampus) revealed that the pattern of changes in these responses in WT mice and DISC1 mutants differed by region. These differences could indicate the vulnerability of DISC1 mutants to stress.

    DOI: 10.3390/ijms23095207

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  121. Polysialylation and disease. 査読有り 国際誌

    Sato C, Kitajima K

    Molecular aspects of medicine   79 巻   頁: 100892 - 100892   2021年6月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Molecular Aspects of Medicine  

    Polysialic acid (polySia, PSA) is a unique constituent of the glycocalyx on the surface of bacterial and vertebrate cells. In vertebrates, its biosynthesis is highly regulated, not only in quantity and quality, but also in time and location, which allows polySia to be involved in various important biological phenomena. Therefore, impairments in the expression and structure of polySia sometimes relate to diseases, such as schizophrenia, bipolar disorder, and cancer. Some bacteria express polySia as a tool for protecting themselves from the host immune system during invasion. PolySia is proven to be a biosafe material; polySia, as well as polySia-recognizing molecules, are key therapeutic agents. This review first comprehensive outlines the occurrence, features, biosynthesis, and functions of polySia and subsequently focuses on the related diseases.

    DOI: 10.1016/j.mam.2020.100892

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  122. Evolutionary conservation of human ketodeoxynonulosonic acid production is independent of sialoglycan biosynthesis. 査読有り 国際共著 国際誌

    Kawanishi K, Saha S, Diaz S, Vaill M, Sasmal A, Siddiqui SS, Choudhury B, Sharma K, Chen X, Schoenhofen IC, Sato C, Kitajima K, Freeze HH, Münster-Kühnel A, Varki A

    The Journal of clinical investigation   131 巻 ( 5 )   2021年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Clinical Investigation  

    Human metabolic incorporation of nonhuman sialic acid (Sia) N-glycolylneuraminic acid into endogenous glycans generates inflammation via preexisting antibodies, which likely contributes to red meat-induced atherosclerosis acceleration. Exploring whether this mechanism affects atherosclerosis in end-stage renal disease (ESRD), we instead found serum accumulation of 2-keto-3-deoxy-d-glycero-d-galacto-2-nonulosonic acid (Kdn), a Sia prominently expressed in cold-blooded vertebrates. In patients with ESRD, levels of the Kdn precursor mannose also increased, but within a normal range. Mannose ingestion by healthy volunteers raised the levels of urinary mannose and Kdn. Kdn production pathways remained conserved in mammals but were diminished by an M42T substitution in a key biosynthetic enzyme, N-acetylneuraminate synthase. Remarkably, reversion to the ancestral methionine then occurred independently in 2 lineages, including humans. However, mammalian glycan databases contain no Kdn-glycans. We hypothesize that the potential toxicity of excess mannose in mammals is partly buffered by conversion to free Kdn. Thus, mammals probably conserve Kdn biosynthesis and modulate it in a lineage-specific manner, not for glycosylation, but to control physiological mannose intermediates and metabolites. However, human cells can be forced to express Kdn-glycans via genetic mutations enhancing Kdn utilization, or by transfection with fish enzymes producing cytidine monophosphate-Kdn (CMP-Kdn). Antibodies against Kdn-glycans occur in pooled human immunoglobulins. Pathological conditions that elevate Kdn levels could therefore result in antibody-mediated inflammatory pathologies.

    DOI: 10.1172/JCI137681

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  123. Exploring the Impact of Ketodeoxynonulosonic Acid in Host-Pathogen Interactions Using Uptake and Surface Display by Nontypeable Haemophilus influenzae. 国際共著 国際誌

    Saha S, Coady A, Sasmal A, Kawanishi K, Choudhury B, Yu H, Sorensen RU, Inostroza J, Schoenhofen IC, Chen X, Münster-Kühnel A, Sato C, Kitajima K, Ram S, Nizet V, Varki A

    mBio   12 巻 ( 1 ) 頁: 1 - 24   2021年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:mBio  

    Surface expression of the common vertebrate sialic acid (Sia) N-acetyl-neuraminic acid (Neu5Ac) by commensal and pathogenic microbes appears structurally to represent “molecular mimicry” of host sialoglycans, facilitating multiple mechanisms of host immune evasion. In contrast, ketodeoxynonulosonic acid (Kdn) is a more ancestral Sia also present in prokaryotic glycoconjugates that are structurally quite dis-tinct from vertebrate sialoglycans. We detected human antibodies against Kdn-termi-nated glycans, and sialoglycan microarray studies found these anti-Kdn antibodies to be directed against Kdn-sialoglycans structurally similar to those on human cell surface Neu5Ac-sialoglycans. Anti-Kdn-glycan antibodies appear during infancy in a pattern similar to those generated following incorporation of the nonhuman Sia N-glycolyl-neuraminic acid (Neu5Gc) onto the surface of nontypeable Haemophilus influenzae (NTHi), a human commensal and opportunistic pathogen. NTHi grown in the presence of free Kdn took up and incorporated the Sia into its lipooligosaccharide (LOS). Surface display of the Kdn within NTHi LOS blunted several virulence attributes of the pathogen, including Neu5Ac-mediated resistance to complement and whole blood kill-ing, complement C3 deposition, IgM binding, and engagement of Siglec-9. Upper air-way administration of Kdn reduced NTHi infection in human-like Cmah null (Neu5Gc-deficient) mice that express a Neu5Ac-rich sialome. We propose a mechanism for the induction of anti-Kdn antibodies in humans, suggesting that Kdn could be a natural and/or therapeutic “Trojan horse” that impairs colonization and virulence phenotypes of free Neu5Ac-assimilating human pathogens. IMPORTANCE All cells in vertebrates are coated with a dense array of glycans often capped with sugars called sialic acids. Sialic acids have many functions, including serving as a signal for recognition of “self” cells by the immune system, thereby guiding an appropriate immune response against foreign “nonself” and/or damaged cells. Several pathogenic bacteria have evolved mechanisms to cloak themselves with sialic acids and evade immune responses. Here we explore a type of sialic acid called “Kdn” (ketodeoxy-nonulosonic acid) that has not received much attention in the past and compare and contrast how it interacts with the immune system. Our results show potential for the use of Kdn as a natural intervention against pathogenic bacteria that take up and coat themselves with external sialic acid from the environment.

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  124. The conserved arginine residue in all siglecs is essential for Siglec-7 binding to sialic acid. 査読有り 国際誌

    Yoshimura A, Hatanaka R, Tanaka H, Kitajima K, Sato C

    Biochemical and biophysical research communications   534 巻   頁: 1069 - 1075   2021年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical and Biophysical Research Communications  

    Siglecs are sialic acid (Sia)-binding immunoglobulin-like lectins; the majority of Siglecs functions as transmembrane receptors on the immune cells via Sia residues. Recently, a new Sia binding site in Siglec-7, termed site 2, where arginine (R) 67 was critical, was identified by computational modeling and biochemical analyses, relative to the primary Sia binding site, termed site 1, containing critical R124. Here, the presence of a new essential R94 residue, which is completely conserved among all identified Siglecs, was demonstrated. A mutation of R94 residue in Siglec-7 led to the disappearance of the Sia binding property, similar to a site 1 mutation (R124A). R94 is close to R67 in site 2, and site 2 mutations at either of them abolished the ligand-binding properties to both gangliosides and glycoproteins. These data suggest that, in addition to site 1, the conserved R residue among Siglecs in site 2 is another functional site.

    DOI: 10.1016/j.bbrc.2020.10.023

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  125. Comparative Studies of Polysialic Acids Derived from Five Different Vertebrate Brains. 査読有り 国際誌

    Yang Y, Murai R, Takahashi Y, Mori A, Hane M, Kitajima K, Sato C

    International journal of molecular sciences   21 巻 ( 22 ) 頁: 1 - 22   2020年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:International Journal of Molecular Sciences  

    Polysialic acid (polySia/PSA) is a linear homopolymer of sialic acid (Sia) that primarily modifies the neural cell adhesion molecule (NCAM) in mammalian brains. PolySia-NCAM not only displays an anti-adhesive function due to the hydration effect, but also possesses a molecule-retaining function via a direct binding to neurologically active molecules. The quality and quantity of polySia determine the function of polySia-NCAM and are considered to be profoundly related to the maintenance of normal brain functions. In this study, to compare the structures of polySia-NCAM in brains of five different vertebrates (mammals, birds, reptiles, amphibians, and fish), we adopted newly developed combinational methods for the analyses. The results revealed that the structural features of polySia considerably varied among different species. Interestingly, mice, as a mammal, possess eminently distinct types of polySia, in both quality and quantity, compared with those possessed by other animals. Thus, the mouse polySia is of larger quantities, of longer and more diverse chain lengths, and of a larger molecular size with higher negative charge, compared with polySia of other species. These properties might enable more advanced brain function. Additionally, it is suggested that the polySia/Sia ratio, which likely reflects the complexity of brain function, can be used as a new promising index to evaluate the intelligence of different vertebrate brains.

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  126. Combinational Analyses with Multiple Methods Reveal the Existence of Several Forms of Polysialylated Neural Cell Adhesion Molecule in Mouse Developing Brains. 査読有り 国際誌

    Mori A, Yang Y, Takahashi Y, Hane M, Kitajima K, Sato C

    International journal of molecular sciences   21 巻 ( 16 ) 頁: 1 - 20   2020年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:International Journal of Molecular Sciences  

    Polysialic acid (polySia/PSA) is an anionic glycan polymer of sialic acid, and it mostly modifies the neural cell adhesion molecule (NCAM) in mammalian brains. Quality and quantity of the polySia of the polySia–NCAM is spatio-temporally regulated in normal brain development and functions, and their impairments are reported to be related to diseases, such as psychiatric disorders and cancers. Therefore, precise understanding of the state of polySia–NCAM structure would lead to the diagnosis of diseases for which their suitable evaluation methods are necessary. In this study, to develop these evaluation methods, structures of polySia–NCAM from mouse brains at six different developmental stages were analyzed by several conventional and newly developed methods. Integrated results of these experiments clearly demonstrated the existence of different types of polySia–NCAMs in developing brains. In addition, combinational analyses were shown to be useful for precise understanding of the quantity and quality of polySia, which can provide criteria for the diagnosis of diseases.

    DOI: 10.3390/ijms21165892

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  127. Discovery of a new sialic acid binding region that regulates Siglec-7. 査読有り 国際共著 国際誌

    Yamakawa N, Yasuda Y, Yoshimura A, Goshima A, Crocker PR, Vergoten G, Nishiura Y, Takahashi T, Hanashima S, Matsumoto K, Yamaguchi Y, Tanaka H, Kitajima K, Sato C

    Scientific reports   10 巻 ( 1 ) 頁: 8647 - 8647   2020年5月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Scientific Reports  

    Siglec-7 is a human CD33-like siglec, and is localised predominantly on human natural killer (NK) cells and monocytes. Siglec-7 is considered to function as an immunoreceptor in a sialic acid-dependent manner. However, the underlying mechanisms linking sialic acid-binding and function remain unknown. Here, to gain new insights into the ligand-binding properties of Siglec-7, we carried out in silico analysis and site-directed mutagenesis, and found a new sialic acid-binding region (site 2 containing R67) in addition to the well-known primary ligand-binding region (site 1 containing R124). This was supported by equilibrium dialysis, STD-NMR experiments, and inhibition analysis of GD3-binding toward Siglec-7 using synthetic sialoglycoconjugates and a comprehensive set of ganglioside-based glycoconjugates. Our results suggest that the two ligand-binding sites are potentially controlled by each other due to the flexible conformation of the C-C′ loop of Siglec-7.

    DOI: 10.1038/s41598-020-64887-4

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  128. Effect of expression alteration in flanking genes on phenotypes of St8sia2-deficient mice. 査読有り 国際誌

    Ikegami K, Saigoh K, Fujioka A, Nagano M, Kitajima K, Sato C, Masubuchi S, Kusunoki S, Shigeyoshi Y

    Scientific reports   9 巻 ( 1 ) 頁: 13634 - 13634   2019年9月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Scientific Reports  

    ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 (ST8SIA2) synthesizes polysialic acid (PSA), which is essential for brain development. Although previous studies reported that St8sia2-deficient mice that have a mixed 129 and C57BL/6 (B6) genetic background showed mild and variable phenotypes, the reasons for this remain unknown. We hypothesized that this phenotypic difference is caused by diversity in the expression or function of flanking genes of St8sia2. A genomic polymorphism and gene expression analysis in the flanking region revealed reduced expression of insulin-like growth factor 1 receptor (Igf1r) on the B6 background than on that of the 129 strain. This observation, along with the finding that administration of an IGF1R agonist during pregnancy increased litter size, suggests that the decreased expression of Igf1r associated with ST8SIA2 deficiency caused lethality. This study demonstrates the importance of gene expression level in the flanking regions of a targeted null allele having an effect on phenotype.

    DOI: 10.1038/s41598-019-50006-5

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  129. Functional roles of ST8SIA3-mediated sialylation of striatal dopamine D(2) and adenosine A(2A) receptors. 査読有り 国際共著

    Lin CY, Lai HL, Chen HM, Siew JJ, Hsiao CT, Chang HC, Liao KS, Tsai SC, Wu CY, Kitajima K, Sato C, Khoo KH, Chern Y

    Translational psychiatry   9 巻 ( 1 ) 頁: 209   2019年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Translational Psychiatry  

    Sialic acids are typically added to the end of glycoconjugates by sialyltransferases. Among the six ST8 α-N-acetyl-neuraminide α-2,8-sialyltransferases (ST8SIA) existing in adult brains, ST8SIA2 is a schizophrenia-associated gene. However, the in vivo substrates and physiological functions of most sialyltransferases are currently unknown. The ST8SIA3 is enriched in the striatum. Here, we showed that ablation of St8sia3 in mice (St8sia3-KO) led to fewer disialylated and trisialylated terminal glycotopes in the striatum of St8sia3-KO mice. Moreover, the apparent sizes of several striatum-enriched G-protein-coupled receptors (GPCRs) (including the adenosine A2A receptor (A2AR) and dopamine D1/D2 receptors (D1R and D2R)) were smaller in St8sia3-KO mice than in WT mice. A sialidase treatment removed the differences in the sizes of these molecules between St8sia3-KO and WT mice, confirming the involvement of sialylation. Expression of ST8SIA3 in the striatum of St8sia3-KO mice using adeno-associated viruses normalized the sizes of these proteins, demonstrating a direct role of ST8SIA3. The lack of ST8SIA3-mediated sialylation altered the distribution of these proteins in lipid rafts and the interaction between D2R and A2AR. Locomotor activity assays revealed altered pharmacological responses of St8sia3-KO mice to drugs targeting these receptors and verified that a greater population of D2R formed heteromers with A2AR in the striatum of St8sia3-KO mice. Since the A2AR-D2R heteromer is an important drug target for several basal ganglia diseases (such as schizophrenia and Parkinson’s disease), the present study not only reveals a crucial role for ST8SIA3 in striatal functions but also provides a new drug target for basal ganglia-related diseases.

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  130. Acute stress-induced change in polysialic acid levels mediated by sialidase in mouse brain. 査読有り

    Abe C, Yi Y, Hane M, Kitajima K, Sato C

    Scientific reports   9 巻 ( 1 ) 頁: 9950   2019年7月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Scientific Reports  

    Stress is an important environmental factor influencing human behaviour and causing several mental disorders. Alterations in the structure of polysialic acid (polySia/PSA) due to genetic alterations in ST8SIA2, which encodes a polySia-synthesizing enzyme, are related to certain mental disorders. However, whether stress as an environmental factor leads to changes in polySia structure is unknown. Here we studied the effects of acute stress on polySia expression and found reductions in both the quantity and quality of polySia in the olfactory bulb and prefrontal cortex, even with short-term exposure to acute stress. The use of inhibitors for sialidase, microglia and astrocytes revealed that these declines were due to a transient action of sialidase from microglia and astrocytes in the olfactory bulb and prefrontal cortex, respectively. These data suggest that sialidase dynamically regulates polySia expression in a brain region-specific manner.

    DOI: 10.1038/s41598-019-46240-6

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  131. N-linked mannose glycoconjugates on shrimp thrombospondin, pmTSP-II, and their involvement in the sperm acrosome reaction. 査読有り 国際共著

    Timklay W, Magerd S, Sato C, Somrit M, Watthammawut A, Senarai T, Weerachatyanukul W, Kitajima K, Asuvapongpatana S

    Molecular reproduction and development   86 巻 ( 4 ) 頁: 440 - 449   2019年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Molecular Reproduction and Development  

    Glycoconjugates in egg extracellular matrices are known to serve several functions in reproductive processes. Here, the presence of N-linked mannose (Man) glycoconjugates on shrimp thrombospondin (pmTSP-II) and their physiological functions were investigated in the black tiger shrimp Penaeus monodon. A molecular analysis of pmTSP-II demonstrated anchorage sites for N-linked glycans in both the chitin-binding and TSP3 domains. The presence of Man residues was verified by concanavalin A lectin histochemistry on the purified fraction of pmTSP-II (250 kDa with protease inhibitor). The function of the Man glycoconjugates was evident by the Con A interference with the pmTSP-II-induced acrosome reaction (AR) as well as by the ability to recover the induction of the AR by the inclusion of Mans in the treatment mixture. In addition, the recombinant proteins of the three signature pmTSP-II domains expressed in E. coli (lacking glycosylation) and mannosidase-treated pmTSP-II showed a minimal ability to initiate the AR response. Together, these results provide evidence of the pivotal role that Man-linked pmTSP-II plays in modulating the shrimp sperm AR, a novel role for a TSP family protein in shrimp reproductive biology.

    DOI: 10.1002/mrd.23122

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  132. Sialic Acids in Neurology. 査読有り

    Sato C, Kitajima K

    Advances in carbohydrate chemistry and biochemistry   76 巻   頁: 1 - 64   2019年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Advances in Carbohydrate Chemistry and Biochemistry  

    Sialic acid (Sia) is involved in many biological activities and commonly occurs as a monosialyl residue at the nonreducing terminal end of glycoconjugates. The loss of activity of UDP-GlcNAc2-epimerase/ManNAc kinase, which is a key enzyme in Sia biosynthesis, is lethal to the embryo, which clearly indicates the importance of Sia in embryogenesis. Occasionally, oligo/polymeric Sia structures such as disialic acid (diSia), oligosialic acid (oligoSia), and polysialic acid (polySia) occur in glycoconjugates. In particular, polySia, a well-known epitope that commonly occurs in neuroinvasive bacteria and vertebrate brains, is one of the most well-known and biologically/neurologically important glycotopes in vertebrates. The biological effects of polySia, especially on neural cell-adhesion molecules, have been well studied, and in-depth knowledge regarding polySia has been accumulated. In addition, the importance of diSia and oligoSia epitopes has been reported. In this chapter, the recent advances in the study of diSia, oligoSia, and polySia residues in glycoproteins in neurology, and their history, definition, occurrence, analytical methods, biosynthesis, and biological functions evaluated by phenotypes of gene-targeted mice, biochemical features, and related diseases are described.

    DOI: 10.1016/bs.accb.2018.09.003

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  133. Structural Biology of Glycans 査読有り

    Sato C, Kato K, Yamaguchi Y, Kohda D, Kato R, Suzuki GN K, Kikuchi K, Hirai G, Kizuka Y, Tanaka K, Nakashima Y, Setou M

    Glycoscience: Basic Science to Applications     頁: 35 - 63   2019年

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    記述言語:英語   掲載種別:論文集(書籍)内論文  

    DOI: 10.1007/978-981-13-5856-2_2

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  134. Preparation and Properties of a Polycyclic p-Quinodimethane with Two Oxygen Bridges and its Radical Cation in Comparison with the Isomeric o-Quinodimethane.

    Sato C, Suzuki S, Okada K, Kozaki M

    Chemistry, an Asian journal   13 巻 ( 23 ) 頁: 3729 - 3736   2018年12月

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    掲載種別:研究論文(学術雑誌)  

    DOI: 10.1002/asia.201801269

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  135. Systems glycomics of adult zebrafish identifies organ-specific sialylation and glycosylation patterns. 査読有り 国際誌

    Yamakawa N, Vanbeselaere J, Chang LY, Yu SY, Ducrocq L, Harduin-Lepers A, Kurata J, Aoki-Kinoshita KF, Sato C, Khoo KH, Kitajima K, Guerardel Y

    Nature communications   9 巻 ( 1 ) 頁: 4647 - 4647   2018年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Nature Communications  

    The emergence of zebrafish Danio rerio as a versatile model organism provides the unique opportunity to monitor the functions of glycosylation throughout vertebrate embryogenesis, providing insights into human diseases caused by glycosylation defects. Using a combination of chemical modifications, enzymatic digestion and mass spectrometry analyses, we establish here the precise glycomic profiles of eight individual zebrafish organs and demonstrate that the protein glycosylation and glycosphingolipid expression patterns exhibits exquisite specificity. Concomitant expression screening of a wide array of enzymes involved in the synthesis and transfer of sialic acids shows that the presence of organ-specific sialylation motifs correlates with the localized activity of the corresponding glycan biosynthesis pathways. These findings provide a basis for the rational design of zebrafish lines expressing desired glycosylation profiles.

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  136. Mental disorders and an acidic glycan-from the perspective of polysialic acid (PSA/polySia) and the synthesizing enzyme, ST8SIA2. 査読有り

    Sato C, Hane M

    Glycoconjugate journal   35 巻 ( 4 ) 頁: 353 - 373   2018年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycoconjugate Journal  

    Mental disorders, such as schizophrenia, bipolar disorder, and autism spectrum disorder, are challenging to manage, worldwide. Understanding the molecular mechanisms underlying these disorders is essential and required. Studies investigating such molecular mechanisms are well performed and important findings are accumulating apace. Based on the fact that these disorders are due in part to the accumulation of genetic and environmental risk factors, consideration of multi-molecular and/or multi-system dependent phenomena might be important. Acidic glycans are an attractive family of molecules for understanding these disorders, because impairment of the fine-tuned glycan system affects a large number of molecules that are deeply involved in normal brain function. One of the candidates of this important family of glycan epitopes in the brain is polysialic acid (PSA/polySia). PSA is a well-known molecule because of its role as an oncodevelopmental antigen and is also widely used as a marker of adult neurogenesis. Recently, several reports have suggested that PSA and PSA-related genes are associated with multiple mental disorders. The relationships among PSA, PSA-related genes, and mental disorders are reviewed here.

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  137. 酸性糖鎖ポリシアル酸の新機能の発見とその応用展開 査読有り

    佐藤 ちひろ

    化学と生物   56 巻   頁: 422 - 431   2018年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  138. Positive selection on schizophrenia-associated ST8SIA2 gene in post-glacial Asia. 査読有り

    Fujito NT, Satta Y, Hane M, Matsui A, Yashima K, Kitajima K, Sato C, Takahata N, Hayakawa T

    PloS one   13 巻 ( 7 ) 頁: e0200278   2018年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:PLoS ONE  

    A number of loci are associated with highly heritable schizophrenia and the prevalence of this mental illness has had considerable negative fitness effects on human populations. Here we focused on one particular schizophrenia-associated gene that encodes a sialyltransferase (ST8SIA2) and is expressed preferentially in the brain with the level being largely determined by three SNPs in the promoter region. It is suggested that the expression level of the ST8SIA2 gene is a genetic determinant of schizophrenia risk, and we found that a geographically differentiated non-risk SNP type (CGC-type) has significantly reduced promoter activity. A newly developed method for detecting ongoing positive selection was applied to the ST8SIA2 genomic region with the identification of an unambiguous sweep signal in a rather restricted region of 18 kb length surrounding the promoter. We also found that while the CGC-type emerged in anatomically modern humans in Africa over 100 thousand years ago, it has increased its frequency in Asia only during the past 20–30 thousand years. These findings support that the positive selection is driven by psychosocial stress due to changing social environments since around the last glacial maximum, and raise a possibility that schizophrenia extensively emerged during the Upper Paleolithic and Neolithic era.

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  139. Different properties of polysialic acids synthesized by the polysialyltransferases ST8SIA2 and ST8SIA4.

    Mori A, Hane M, Niimi Y, Kitajima K, Sato C

    Glycobiology   27 巻 ( 9 ) 頁: 834 - 846   2017年9月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    Polysialic acid (polySia) is mainly found as a modification of neural cell adhesion molecule (NCAM) in whole embryonic brains, as well as restricted areas of adult vertebrate brains, including the hippocampus. PolySia shows not only repulsive effects on NCAM-involved cell–cell interactions due to its bulky and hydrated properties, but also attractive effects on the interaction with neurologically active molecules, which exerts a reservoir function. Two different polysialyltransferases, ST8SIA2 and ST8SIA4, are involved in the synthesis of polySia chains; however, to date, the differences of the properties between polySia chains synthesized by these two enzymes remain unknown. In this study, to clarify this point, we first prepared polySia-NCAMs from HEK293 cells stably expressing ST8SIA4 and ST8SIA2, or ST8SIA2 (SNP-7), a mutant ST8SIA2 derived from a schizophrenia patient. The conventional sensitive chemical and immunological characterizations showed that the quantity and quality (structural features) of polySia are not so much different between ST8SIA4- and ST8SIA2-synthesized ones, apart from those of ST8SIA2 (SNP-7). Then, we assessed the homophilic and heterophilic interactions mediated by polySia-NCAM by adopting a surface plasmon resonance measurement as an in vitro analytical method. Our novel findings are as follows: (i) the ST8SIA2- and ST8SIA4-synthesized polySia-NCAMs exhibited different attractive and repulsive effects than each other; (ii) both polySia- and oligoSia-NCAMs synthesized by ST8SIA2 were able to bind polySia-NCAMs; (iii) the polySia-NCAM synthesized by a ST8SIA2 (SNP-7) showed markedly altered attractive and repulsive properties. Collectively, polySia-NCAM is suggested to simultaneously possess both attractive and repulsive properties that are highly regulated by the two polysialyltransferases.

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  140. Chemical Synthesis and Evaluation of a Disialic Acid-Containing Dextran Polymer as an Inhibitor for the Interaction between Siglec 7 and Its Ligand.

    Yamaguchi S, Yoshimura A, Yasuda Y, Mori A, Tanaka H, Takahashi T, Kitajima K, Sato C

    Chembiochem : a European journal of chemical biology   18 巻 ( 13 ) 頁: 1194 - 1203   2017年7月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:ChemBioChem  

    A new sialic acid (Sia)-containing glycopolymer—a fluorescent probe with high-density disialic acid (diSia) on the surface of polysaccharide dextran (diSia-Dex)—was synthesized as a key molecule to regulate the Sia recognition lectins, Siglecs, that are involved in the immune system. According to our original methods, diSia was synthesized by α-selective sialylation, and a dextran template possessing terminal acetylenes and amino groups was prepared. A diSia and a fluorescent molecule were subsequently introduced to surface-modified dextran by Hüisgen reaction and amidation, respectively. The modulatory activity of Siglec7 was evaluated by using synthetic probes. DiSia-Dex showed high binding avidity toward Siglec7, with a KD value of 5.87×10−10 m, and a high inhibitory activity for the interaction between Siglec7 and a ligand (GD3), with a IC50 value of 1.0 nm. Notably, diSia-Dex was able to release Siglec7 from the pre-existing Siglec7–GD3 complex, possibly due to its unique properties of a slow dissociation rate and a high association rate. Together, these data show that diSia-Dex can be widely applicable as a modulator of Siglec7 functions.

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  141. Alpha-2 macroglobulin as a region-specific secretory protein in male reproductive tract, and its dynamics during sperm transit toward the female spermatheca in the blue crab.

    Senarai T, Vanichviriyakit R, Miyata S, Sato C, Sretarugsa P, Weerachatyanukul W, Kitajima K

    Molecular reproduction and development   84 巻 ( 7 ) 頁: 585 - 595   2017年7月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Molecular Reproduction and Development  

    A 250-kDa protein was isolated from fluid in the middle spermatic duct (MSD) of the blue crab (Portunus pelagicus). N-terminal and partial amino acid sequences revealed that this MSD-specific protein is highly similar to the plasma-enriched protein Alpha-2 macroglobulin (α2M). The P. pelagicus ortholog (Ppα2M) is a large glycoprotein possessing mannose and N-acetylglucosamine residues. Ppa2m mRNA was detected in the spermatic duct, androgenic gland, and hematopoietic tissue, whereas the protein was primarily observed in the apical cytoplasm of MSD epithelium and in the matrix of the acrosome of MSD sperm; distally within spermatic duct, Ppα2M was lost from the sperm membrane but remained in the sperm acrosome. These results suggest that Ppα2M is expressed and glycosylated in the epithelium of spermatic ducts, secreted into MSD fluid, taken up by sperm in the MSD, and removed from the surface of sperm during its transit towards the female spermatheca. Given that Ppα2M also exhibits protease inhibitor activity, we hypothesize that acrosome localized Ppα2M may suppress premature acrosome reaction during post-testicular sperm maturation in this crab.

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  142. Chlorpromazine Increases the Expression of Polysialic Acid (PolySia) in Human Neuroblastoma Cells and Mouse Prefrontal Cortex.

    Abe C, Nishimura S, Mori A, Niimi Y, Yang Y, Hane M, Kitajima K, Sato C

    International journal of molecular sciences   18 巻 ( 6 )   2017年5月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:International Journal of Molecular Sciences  

    The neural cell adhesion molecule (NCAM) is modified by polysialic acid (polySia or PSA) in embryonic brains. In adult brains, polySia modification of NCAM is only observed in restricted areas where neural plasticity, remodeling of neural connections, or neural generation is ongoing although the amount of NCAM remains unchanged. Impairments of the polySia-expression and several single nucleotide polymorphisms (SNPs) of the polysialyltransferase (polyST) ST8SIA2 gene are reported to be associated with schizophrenia and bipolar disorder. Chlorpromazine (CPZ) is well-known as an agent for treating schizophrenia, and our hypothesis is that CPZ may affect the polySia expression or the gene expression of polySTs or NCAM. To test this hypothesis, we analyzed the effects of CPZ on the expression of polySia-NCAM on human neuroblastoma cell line, IMR-32 cells, by immunochemical and chemical methods. Interestingly, the cell surface expression of polySia, especially those with lower chain lengths, was significantly increased on the CPZ-treated cells, while mRNAs for polySTs and NCAM, and the amounts of total polySia-NCAM remained unchanged. The addition of brefeldin A, an inhibitor of endocytosis, suppressed the CPZ-induced cell surface polySia expression. In addition, polySia-NCAM was also observed in the vesicle compartment inside the cell. All these data suggest that the level of cell surface expression of polySia in IMR-32 is highly regulated and that CPZ changes the rate of the recycling of polySia-NCAM, leading to the up-regulation of polySia-NCAM on the cell surface. We also analyzed the effect of CPZ on polySia-expression in various brain regions in adult mice and found that CPZ only influenced the total amounts of polySia-NCAM in prefrontal cortex. These results suggest a brain-region-specific effect of CPZ on the expression of total polySia in mouse brain. Collectively, anti-schizophrenia agent CPZ consistently up-regulates the expression polySia at both cellular and animal levels.

    DOI: 10.3390/ijms18061123

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  143. Altered expression of ganglioside GM3 molecular species and a potential regulatory role during myoblast differentiation.

    Go S, Go S, Veillon L, Ciampa MG, Mauri L, Sato C, Kitajima K, Prinetti A, Sonnino S, Inokuchi JI

    The Journal of biological chemistry   292 巻 ( 17 ) 頁: 7040 - 7051   2017年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    Gangliosides (sialic acid-containing glycosphingolipids) help regulate many important biological processes, including cell proliferation, signal transduction, and differentiation, via formation of functional microdomains in plasma membranes. The structural diversity of gangliosides arises from both the ceramide moiety and glycan portion. Recently, differing molecular species of a given ganglioside are suggested to have distinct biological properties and regulate specific and distinct biological events. Elucidation of the function of each molecular species is important and will provide new insights into ganglioside biology. Gangliosides are also suggested to be involved in skeletal muscle differentiation; however, the differential roles of ganglioside molecular species remain unclear. Here we describe striking changes in quantity and quality of gangliosides (particularly GM3)during differentiation of mouse C2C12 myoblast cells and key roles played by distinct GM3 molecular species at each step of the process.

    DOI: 10.1074/jbc.M116.771253

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  144. Diverse subcellular localizations of the insect CMP-sialic acid synthetases.

    Di W, Fujita A, Hamaguchi K, Delannoy P, Sato C, Kitajima K

    Glycobiology   27 巻 ( 4 ) 頁: 329 - 341   2017年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    The occurrence and biological importance of sialic acid (Sia) and its metabolic enzymes in insects have been studied using Drosophila melanogaster. The most prominent feature of D. melanogaster CMP-Sia synthetase (DmCSS) is its Golgi-localization, contrasted with nuclear localization of vertebrate CSSs. However, it remains unclear if the Golgi-localization is common to other insect CSSs and why it happens. To answer these questions, Aedes aegypti (mosquito) CSS (AaCSS) and Tribolium castaneum (beetle) CSS (TcCSS) were cloned and characterized for their activity and subcellular localization. Our new findings show: (1) AaCSS and TcCSS share a common overall structure with DmCSS in terms of evolutionarily conserved motifs and the absence of the C-terminal domain typical to vertebrate CSSs; (2) when expressed in mammalian and insect cells, AaCSS and TcCSS showed in vivo and in vitro CSS activities, similar to DmCSS. In contrast, when expressed in bacteria, they lacked CSS activity because the N-terminal hydrophobic region appeared to induce protein aggregation; (3) when expressed in Drosophila S2 cells, AaCSS and TcCSS were predominantly localized in the ER, but not in the Golgi. Surprisingly, DmCSS was mainly secreted into the culture medium, although partially detected in Golgi. Consistent with these results, the N-terminal hydrophobic regions of AaCSS and TcCSS functioned as a signal peptide to render them soluble in the ER, while the N-terminus of DmCSS functioned as a membrane-spanning region of type II transmembrane proteins whose cytosolic KLK sequence functioned as an ER export signal. Accordingly, the differential subcellular localization of insect CSSs are distinctively more diverse than previously recognized.

    DOI: 10.1093/glycob/cww128

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  145. Synthesis of end-functionalized glycopolymers containing α(2,8) disialic acids via π-allyl nickel catalyzed coordinating polymerization and their interaction with Siglec-7. 査読有り

    Ohira S, Yasuda Y, Tomita I, Kitajima K, Takahashi T, Sato C, Tanaka H

    Chemical communications (Cambridge, England)   53 巻 ( 3 ) 頁: 553 - 556   2017年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Chemical Communications  

    An allene monomer containing an α(2,8) disialic acid was polymerized by a π-allyl nickel complex with an azido group to produce end-functional glycopolymers with an excellent polydispersity index. The polymers allowed terminal modification with a fluorescent dye by click chemistry. The glycopolymers can dissociate Siglec-7-GD3 interactions at low concentrations.

    DOI: 10.1039/c6cc07115e

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  146. Synthesis of end-functionalized glycopolymers containing α(2,8) disialic acids via π-allyl nickel catalyzed coordinating polymerization and their interaction with Siglec-7. 査読有り

    Ohira S, Yasuda Y, Tomita I, Kitajima K, Takahashi T, Sato C, Tanaka H.

    Chem Commun (Camb).   53 巻 ( 3 ) 頁: 553-556.   2017年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  147. Releasing Mechanism of Neurotrophic Factors via Polysialic Acid.

    Sato C

    Vitamins and hormones   104 巻   頁: 89 - 112   2017年

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    記述言語:英語   掲載種別:論文集(書籍)内論文   出版者・発行元:Vitamins and Hormones  

    Neurotrophins are well-characterized neurologically active molecules in the central nervous system. The regulation of these signaling molecules, which are involved in cell growth, differentiation, and survival, is critical for normal brain function. Among the different types of neurotrophins, brain-derived neurotrophic factor (BDNF) is involved in various brain functions, including memory consolidation, synaptic plasticity, and adult neurogenesis, and is therefore a key molecule for understanding comprehensive brain function and neurodevelopmental and psychiatric diseases. The concentration of BDNF in body fluid is highly related to several neurodevelopmental and psychiatric diseases, including Alzheimer's diseases, depression, schizophrenia, and bipolar disorder. In the present review, the mechanisms by which BDNF is released from secretory vesicles are reviewed, with a particular focus on the recently described glycan-mediated release. In addition, the impact of glycan-mediated BDNF release on psychiatric disorders is also discussed.

    DOI: 10.1016/bs.vh.2016.11.004

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  148. ポリシアル酸転移酵素遺伝子ST8SIA2と精神疾患の関わり 査読有り

    羽根正弥, 北島 健, 佐藤 ちひろ

    生化学   89 巻   頁: 634 - 643   2017年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  149. Diverse subcellular localizations of the insect CMP-sialic acid synthetases. 査読有り

    Di W, Fujita A, Hamaguchi K, Delannoy P, Sato C, Kitajima K.

    Glycobiology.     2016年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: doi: 10.1093/glycob/cww128.

  150. Effects of intronic single nucleotide polymorphisms (iSNPs) of a polysialyltransferase, ST8SIA2 gene found in psychiatric disorders on its gene products. 査読有り

    Hane M, Kitajima K, Sato C

    Biochemical and biophysical research communications   478 巻 ( 3 ) 頁: 1123 - 9   2016年9月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical and Biophysical Research Communications  

    Polysialic acid (polySia) is a linear homopolymer of sialic acid and mainly modifies neural cell adhesion molecule. PolySia plays important roles in synapse formation, learning and memory, social behavior and is associated with several diseases. Gene analyses of one of the biosynthetic enzymes for polySia, ST8SIA2, have revealed that several SNPs and genetic variations in the ST8SIA2 gene are associated with several psychiatric disorders; however, the mechanisms underlying these associations remain unknown. Here, we analyzed the effects of two iSNPs of ST8SIA2, rs2168351 and rs3784730, which are associated with bipolar disorder and autism spectrum disorder, respectively, on the expression of mRNA, ST8SIA2 and its final product, polySia in mouse neuroblastoma and human adenocarcinoma cell lines. We found that both iSNPs affected the expression of pre-mRNA and mRNA of ST8SIA2, and altered the cellular levels of ST8SIA2 and polySia. Taken together, these results indicate that impairment of the regulated expression of ST8SIA2 and the resulting downstream effects on gene products by these two iSNPs contribute to the development of these psychiatric disorders.

    DOI: 10.1016/j.bbrc.2016.08.079

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  151. Effects of intronic single nucleotide polymorphisms (iSNPs) of a polysialyltransferase, ST8SIA2 gene found in psychiatric disorders on its gene products. 査読有り

    Hane M, Kitajima K, Sato C.

    Biochem Biophys Res Commun.   478 巻 ( 3 ) 頁: 1123-9.   2016年9月

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: doi: 10.1016/j.bbrc.2016.08.079.

  152. Relationship between ST8SIA2, polysialic acid and its binding molecules, and psychiatric disorders

    Sato C.

    Biochimica et Biophysica Acta - General Subjects   1860 巻 ( 8 ) 頁: 1739 - 1752   2016年8月

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    掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochimica et Biophysica Acta - General Subjects  

    DOI: 10.1016/j.bbagen.2016.04.015

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  153. Relationship between ST8SIA2, polysialic acid and its binding molecules, and psychiatric disorders. 招待有り 査読有り

    Sato C, Hane M, Kitajima K.

    Biochim Biophys Acta.   1860 巻 ( 8 ) 頁: 1739-52   2016年8月

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: doi: 10.1016/j.bbagen.2016.04.015.

  154. Relationship between ST8SIA2, polysialic acid and its binding molecules, and psychiatric disorders.

    Sato C, Hane M, Kitajima K

    Biochimica et biophysica acta   1860 巻 ( 8 ) 頁: 1739 - 52   2016年8月

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    掲載種別:研究論文(学術雑誌)  

    DOI: 10.1016/j.bbagen.2016.04.015

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  155. Relationship between ST8SIA2, polysialic acid and its binding molecules, and psychiatric disorders. 査読有り

    Sato C, Hane M, Kitajima K

    Biochimica et biophysica acta   1860 巻 ( 8 ) 頁: 1739 - 1752   2016年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1016/j.bbagen.2016.04.015

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  156. Relationship between ST8SIA2, polysialic acid and its binding molecules, and psychiatric disorders 査読有り

    Chihiro Sato, Masaya Hane, Ken Kitajima

    BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS   1860 巻 ( 8 ) 頁: 1739 - 1752   2016年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:ELSEVIER SCIENCE BV  

    Polysialic acid (polySia, PSA) is a unique and functionally important glycan, particularly in vertebrate brains. It is involved in higher brain functions such as learning, memory, and social behaviors. Recently, an association between several genetic variations and single nucleotide polymorphisms (SNPs) of ST8SIA2/STX, one of two polysialyltransferase genes in vertebrates, and psychiatric disorders, such as schizophrenia (SZ), bipolar disorder (BD), and autism spectrum disorder (ASD), was reported based on candidate gene approaches and genome-wide studies among normal and mental disorder patients. It is of critical importance to determine if the reported mutations and SNPs in ST8SIA2 lead to impairments of the structure and function of polySia, which is the final product of ST8SIA2. To date, however, only a few such forward-directed studies have been conducted. In addition, the molecular mechanisms underlying polySia-involved brain functions remain unknown, although polySia was shown to have an anti-adhesive effect. In this report, we review the relationships between psychiatric disorders and polySia and/or ST8SIA2, and describe a new function of polySia as a regulator of neurologically active molecules, such as brain-derived neurotrophic factor (BDNF) and dopamine, which are deeply involved in psychiatric disorders. This article is part of a Special Issue entitled "Glycans in personalised medicine" Guest Editor: Professor Gordan Lauc. (C) 2016 Elsevier B.V. All rights reserved.

    DOI: 10.1016/j.bbagen.2016.04.015

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  157. Relationship between ST8SIA2, polysialic acid and its binding molecules, and psychiatric disorders

    Sato Chihiro, Hane Masaya, Kitajima Ken

    BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS   1860 巻 ( 8 ) 頁: 1739 - 1752   2016年8月

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    掲載種別:研究論文(学術雑誌)  

    DOI: 10.1016/j.bbagen.2016.04.015

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  158. The AMOR Arabinogalactan Sugar Chain Induces Pollen-Tube Competency to Respond to Ovular Guidance. 査読有り 国際誌

    Mizukami AG, Inatsugi R, Jiao J, Kotake T, Kuwata K, Ootani K, Okuda S, Sankaranarayanan S, Sato Y, Maruyama D, Iwai H, Garénaux E, Sato C, Kitajima K, Tsumuraya Y, Mori H, Yamaguchi J, Itami K, Sasaki N, Higashiyama T

    Current biology : CB   26 巻 ( 8 ) 頁: 1091 - 7   2016年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Current Biology  

    Precise directional control of pollen-tube growth by pistil tissue is critical for successful fertilization of flowering plants [1-3]. Ovular attractant peptides, which are secreted from two synergid cells on the side of the egg cell, have been identified [4-6]. Emerging evidence suggests that the ovular directional cue is not sufficient for successful guidance but that competency control by the pistil is critical for the response of pollen tubes to the attraction signal [1, 3, 7]. However, the female molecule for this competency induction has not been reported. Here we report that ovular methyl-glucuronosyl arabinogalactan (AMOR) induces competency of the pollen tube to respond to ovular attractant LURE peptides in Torenia fournieri. We developed a method for assaying the response capability of a pollen tube by micromanipulating an ovule. Using this method, we showed that pollen tubes growing through a cut style acquired a response capability in the medium by receiving a sufficient amount of a factor derived from mature ovules of Torenia. This factor, named AMOR, was identified as an arabinogalactan polysaccharide, the terminal 4-O-methyl-glucuronosyl residue of which was necessary for its activity. Moreover, a chemically synthesized disaccharide, the β isomer of methyl-glucuronosyl galactose (4-Me-GlcA-β-(1→6)-Gal), showed AMOR activity. No specific sugar-chain structure of plant extracellular matrix has been identified as a bioactive molecule involved in intercellular communication. We suggest that the AMOR sugar chain in the ovary renders the pollen tube competent to the chemotropic response prior to final guidance by LURE peptides.

    DOI: 10.1016/j.cub.2016.02.040

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  159. .The AMOR Arabinogalactan Sugar Chain Induces Pollen-Tube Competency to Respond to Ovular Guidance. 査読有り

    Mizukami AG, Inatsugi R, Jiao J, Kotake T, Kuwata K, Ootani K, Okuda S, Sankaranarayanan S, Sato Y, Maruyama D, Iwai H, Garénaux E, Sato C, Kitajima K, Tsumuraya Y, Mori H, Yamaguchi J, Itami K, Sasaki N, Higashiyama T

    Curr Biol.   26 巻 ( 8 ) 頁: 1091-7   2016年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  160. 2,11-Dibromo-13,14-dimesityl-5,8-dioxapentaphene: A Stable and Twisted Polycyclic System Containing the o-Quinodimethane Skeleton.

    Sato C, Suzuki S, Kozaki M, Okada K

    Organic letters   18 巻 ( 5 ) 頁: 1052 - 5   2016年3月

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    掲載種別:研究論文(学術雑誌)  

    DOI: 10.1021/acs.orglett.6b00171

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  161. Flagellasialin: Highly Glycosylated Gpi-Anchored Protein Involved in Intracellular Ca<sup>2+</sup> Regulation in Sea Urchin Sperm 査読有り

    Kanazawa T., Suzuki E., Miyata S., Sato C., Kitajima K.

    Glycoscience: Biology and Medicine     頁: 883 - 890   2015年1月

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    記述言語:英語   掲載種別:論文集(書籍)内論文   出版者・発行元:Glycoscience: Biology and Medicine  

    Very little knowledge has been available on structure and function of heavily glycosylated proteins, whose glycan parts amount to more than 90 % of the whole molecules, mainly because of technical difficulties in detection and determination of structure. In 2004 flagellasialin was discovered as a major cell surface component in the lipid rafts of sea urchin sperm. The extremely high content of glycan chains completely prevented detecting this glycoprotein by conventional protein staining methods, such as Coomassie Brilliant Blue and silver staining. To make this glycoprotein visible, monoclonal antibodies 4F7 and 3G9 were developed as specific probes for detecting glycan chains of flagellasialin. The frequent occurrence of GPI-anchored proteins in lipid rafts is well recognized. Flagellasialin was actually demonstrated to contain a GPI-anchor, based on three lines of experiments. In addition to the computational predictions from the cDNA sequence and the phosphatidylinositolspecific phospholipase C treatment of the sperm membrane fraction, nitrous acid deamination of a flagellasialin-blotted membrane was newly introduced. The immunostaining of flagellasialin on the membrane disappeared after the nitrous acid treatment of the blotted membrane. This method was easy and effective for identifying flagellasialin as a GPI-anchored protein.

    DOI: 10.1007/978-4-431-54841-6_167

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  162. Polysialyltransferase assay 査読有り

    Hane M., Kitajima K., Sato C.

    Glycoscience: Biology and Medicine     頁: 529 - 534   2015年1月

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    記述言語:英語   掲載種別:論文集(書籍)内論文   出版者・発行元:Glycoscience: Biology and Medicine  

    It has been shown that polysialic acid (polySia) is an indispensable component for viability of mouse during development. Especially, it is deeply involved in normal brain function in mouse and human, affecting cell adhesion, cell migration, cell growth, neurogenesis, and synaptogenesis. PolySia is synthesized by two polysialyltransferases, ST8SIA2 and ST8SIA4. Mice deficient in both enzymes show lethality soon after birth. Mice deficient in either ST8SIA2 or ST8SIA4 show significant impairments in learning, memory, circadian rhythm, and social behavior. Interestingly, different phenotypes are often observed between ST8SIA2- and ST8SIA4-deficient mice. Therefore, characterization of these enzymes in vitro and in vivo and precise understanding of the structurefunction relationship of polySia become more and more important. In this chapter, assay procedures for in vitro activity of the polysialyltransferases are focused on to obtain clear results of their in vitro activities that are often said to be very weak compared with other sialyltransferases.

    DOI: 10.1007/978-4-431-54841-6_118

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  163. Polysialic acid 査読有り

    Sato C., Kitajima K.

    Glycoscience: Biology and Medicine     頁: 519 - 528   2015年1月

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    記述言語:英語   掲載種別:論文集(書籍)内論文   出版者・発行元:Glycoscience: Biology and Medicine  

    Polysialic acid (polySia), particularly α2,8-linked polyNeu5Ac (DP ¼ 8 ~ 400), is a unique polymer of sialic acid (Sia) and modifies neural cell adhesion molecule (NCAM) spatiotemporally in embryonic brains. PolySia is involved in cell migration, neural outgrowth, axonal guidance, synaptic plasticity, and the development of normal neural circuits and neurogenesis due to its anti- adhesive property and spatiotemporal expression. Recent improvements of polySia-detection methods have told us that polySia expression persists in certain areas of the adult brain, such as the olfactory bulb, hippocampus, subventricular zone, thalamus, prefrontal cortex, and amygdala, where neural plasticity, remodeling of neural connections, or neural generation is ongoing. Importantly, several lines of evidence have raised a new concept of polySia function that polySia works as an attractive field that associates with particular ion channels and neurologically active molecules, such as neurotrophic factor (BDNF), growth factor (FGF2), and neurotransmitter (dopamine), to regulate their involved signaling. It has been shown that polySia is involved in learning, memory, circadian rhythm, and social behaviors using polySia-impaired mice. In addition, SNPs and some deletions in genes encoding the polysialyltransferase and NCAM have been reported from patients of schizophrenia, mood disorder and autism. Such impairments of polySia structure derived from polysialyltransferase gene alterations might influence the polySia function not only as the repulsive field but also as the attractive field.

    DOI: 10.1007/978-4-431-54841-6_117

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  164. Discovery, primary, and crystal structures and capacitation-related properties of a prostate-derived heparin-binding protein WGA16 from boar sperm. 査読有り

    Garénaux E, Kanagawa M, Tsuchiyama T, Hori K, Kanazawa T, Goshima A, Chiba M, Yasue H, Ikeda A, Yamaguchi Y, Sato C, Kitajima K.

    J Biol Chem.   290 巻   頁: 5484-501   2015年

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  165. Protective effects of polysialic acid on proteolytic cleavage of FGF2 and proBDNF/BDNF. 査読有り

    Hane M, Matsuoka S, Ono S, Miyata S, Kitajima K, Sato C.

    Glycobiology   25 巻   頁: 1112-24   2015年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  166. Sulfatide-Hsp70 interaction promotes Hsp70 clustering and stabilizes binding to unfolded protein. 査読有り

    Harada Y, Sato C, Kitajima K.

    Biomolecules.   5 巻   頁: 958-73   2015年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  167. Ganglioside contained in the neuronal tissue-enriched acidic protein of 22 kDa (NAP-22) fraction prepared from the detergent-resistant membrane microdomain of rat brain inhibits the phosphatase activity of calcineurin. 査読有り

    Kobayashi Y, da Silva R, Kumanogoh H, Miyata S, Sato C, Kitajima K, Nakamura S, Morita M, Hayashi F, Maekawa S.

    J Neurosci Res.   93 巻   頁: 1462-70   2015年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  168. Rapid Trimming of Cell Surface Polysialic Acid (PolySia) by Exovesicular Sialidase Triggers Release of Preexisting Surface Neurotrophin. 査読有り

    Sumida M, Hane M, Yabe U, Shimoda Y, Pearce OM, Kiso M, Miyagi T, Sawada M, Varki A, Kitajima K, Sato C.

    J Biol Chem.   290 巻   頁: 13202-14   2015年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  169. Sulfatide-Hsp70 interaction promotes Hsp70 clustering and stabilizes binding to unfolded protein. 査読有り

    Harada Y, Sato C, Kitajima K

    Biomolecules.   5 巻   頁: 958-73   2015年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  170. Advanced Technologies in Sialic Acid and Sialoglycoconjugate Analysis. 査読有り

    Kitajima K, Varki N, Sato C

    Topics in current chemistry   367 巻   頁: 75 - 103   2015年

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    記述言語:英語   掲載種別:論文集(書籍)内論文   出版者・発行元:Topics in Current Chemistry  

    Although the structural diversity of sialic acid (Sia) is rapidly expanding, understanding of its biological significance has lagged behind. Advanced technologies to detect and probe diverse structures of Sia are absolutely necessary not only to understand further biological significance but also to pursue medicinal and industrial applications. Here we describe analytical methods for detection of Sia that have recently been developed or improved, with a special focus on 9-O-acetylated N-acetylneuraminic acid (Neu5,9Ac), N-glycolylneuraminic acid (Neu5Gc), deaminoneuraminic acid (Kdn),O-sulfated Sia (SiaS), and di-, oligo-, and polysialic acid (diSia/oligoSia/polySia) in glycoproteins and glycolipids. Much more attention has been paid to these Sia and sialoglycoconjugates during the last decade, in terms of regulation of the immune system, neural development and function, tumorigenesis, and aging.

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  171. Discovery, primary, and crystal structures and capacitation-related properties of a prostate-derived heparin-binding protein WGA16 from boar sperm. 査読有り

    Garénaux E, Kanagawa M, Tsuchiyama T, Hori K, Kanazawa T, Goshima A, Chiba M, Yasue H, Ikeda A, Yamaguchi Y, Sato C, Kitajima K

    J Biol Chem.   290 巻   頁: 5484-501   2015年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  172. Rapid Trimming of Cell Surface Polysialic Acid (PolySia) by Exovesicular Sialidase Triggers Release of Preexisting Surface Neurotrophin. 査読有り

    Sumida M, Hane M, Yabe U, Shimoda Y, Pearce OM, Kiso M, Miyagi T, Sawada M, Varki A, Kitajima K, Sato C

    J Biol Chem.   290 巻   頁: 13202-14   2015年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  173. Protective effects of polysialic acid on proteolytic cleavage of FGF2 and proBDNF/BDNF. 査読有り

    Hane M, Matsuoka S, Ono S, Miyata S, Kitajima K, Sato C

    Glycobiology   25 巻   頁: 1112-24   2015年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  174. Ganglioside contained in the neuronal tissue-enriched acidic protein of 22 kDa (NAP-22) fraction prepared from the detergent-resistant membrane microdomain of rat brain inhibits the phosphatase activity of calcineurin. 査読有り

    Kobayashi Y, da Silva R, Kumanogoh H, Miyata S, Sato C, Kitajima K, Nakamura S, Morita M, Hayashi F, Maekawa S

    J Neurosci Res.   93 巻   頁: 1462-70   2015年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  175. Tissue-specific posttranslational modification allows functional targeting of thyrotropin. 査読有り

    Ikegami K, Liao XH, Hoshino Y, Ono H, Ota W, Ito Y, Nishiwaki-Ohkawa T, Sato C, Kitajima K, Iigo M, Shigeyoshi Y, Yamada M, Murata Y, Refetoff S, Yoshimura T

    Cell reports   9 巻 ( 3 ) 頁: 801 - 10   2014年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Cell Reports  

    Thyroid-stimulating hormone (TSH; thyrotropin) is a glycoprotein secreted from the pituitary gland. Pars distalis-derived TSH (PD-TSH) stimulates the thyroid gland to produce thyroid hormones (THs), whereas pars tuberalis-derivedTSH(PT-TSH) actsonthe hypothalamus to regulate seasonal physiology and behavior. However, it had not been clear how these two TSHs avoid functional crosstalk. Here, we show that this regulation ismediated by tissue-specific glycosylation. AlthoughPT-TSHis releasedinto the circulation, it does not stimulate the thyroid gland. PD-TSH is known to have sulfated biantennary N-glycans, and sulfated TSH is rapidly metabolized in the liver. In contrast, PT-TSH has sialylated multibranched N-glycans; in the circulation, it forms the macro-TSH complex with immunoglobulin or albumin, resulting in the loss of its bioactivity. Glycosylation is fundamental to awide range of biological processes. This report demonstrates its involvement in preventing functional crosstalk of signaling molecules in the body.

    DOI: 10.1016/j.celrep.2014.10.006

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  176. Critical importance of the surface expression of alpha 2,6-sialosides during early development of medaka fish

    Kitajima Ken, Wu Di, Tajima Katsue, Maruyama Emi, Yasukawa Yuko, Chang Lan-Yi, Taniguchi Yoshihito, Kamei Yasuhiro, Adachi Tomoko, Hashimoto Hisashi, Hibi Masahiko, Fujita Akiko, Sato Chihiro

    GLYCOBIOLOGY   24 巻 ( 11 ) 頁: 1110-1110   2014年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  177. Interaction of 70-kDa heat shock protein with glycosaminoglycans and acidic glycopolymers. 査読有り

    Harada Y, Garenáux E, Nagatsuka T, Uzawa H, Nishida Y, Sato C, Kitajima K

    Biochemical and biophysical research communications   453 巻 ( 2 ) 頁: 229 - 34   2014年10月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical and Biophysical Research Communications  

    Interaction of Hsp70 with natural and artificial acidic glycans is demonstrated based on the native PAGE analysis. Hsp70 interacts with acidic glycopolymers that contain clustered sulfated and di-sialylated glycan moieties on a polyacrylamide backbone, but not with neutral or mono-sialylated glycopolymers. Hsp70 also interacts and forms a large complex with heparin, heparan sulfate, and dermatan sulfate that commonly contain 2-O-sulfated iduronic acid residues, but not with other types of glycosaminoglycans (GAGs). Hsp70 consists of the N-terminal ATPase domain and the C-terminal peptide-binding domain. The interaction analyses using the recombinant N- and C-terminal half domains show that the ATPase domain mediates the direct interaction with acidic glycans, while the peptide-binding domain stabilizes the large complexes with particular GAGs. To our knowledge, this is the first demonstration of direct binding of Hsp70 to the particular GAGs. This property may be involved in the physiological functions of Hsp70 at the plasma membrane and extracellular environments.

    DOI: 10.1016/j.bbrc.2014.05.137

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  178. ST8 alpha-N-acetyl-neuraminide alpha- 2,8-sialyltransferase 2 (ST8SIA2)

    Sato C.

    Handbook of Glycosyltransferases and Related Genes, Second Edition   2 巻   頁: 781-795   2014年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1007/978-4-431-54240-7_77

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  179. Polysialic acid: Biosynthesis, novel functions and applications. 査読有り

    Colley K., Kitajima K, Sato C.

    Critical Reviews in Biochemistry and Molecular Biology     頁: 1-35   2014年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  180. Tissue-specific post-translational modification allows functional targeting of thyrotropin. 査読有り

    Ikegami K, Liao X-H, Hoshino Y, Ono H, Ota W, Ito Y, Nishiwaki-Ohkawa T, Sato C, Kitajima K, Iigo M, Shigeyoshi Y, Yamada M, Murata Y, Refetoff S, Yoshimura T.

    Cell Reports   9 巻   頁: 1-9   2014年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  181. Comparison of analytical methods to detect polysialic acid. 査読有り

    Nishimura S, Hane M, Niimi Y, Miyata S, Kitajima K, and Sato C.

    Journal of Glycomics and Lipidomics   4 巻   頁: 113   2014年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  182. Interaction of 70-kDa heat shock protein with glycosaminoglycans and acidc glycopolymers. 査読有り

    Harada Y, Garenaux E, Nagatsuka T, Uzawa H, Nishida Y, Sato C, and Kitajima K.

    Biochem Biophys Res Commun.   453 巻   頁: 229-234   2014年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  183. Frontal affinity chromatography: practice of weak interaction analysis between lectins and fluorescently labeled oligosaccharides. 査読有り

    Sato C

    Methods in molecular biology (Clifton, N.J.)   1200 巻   頁: 257 - 64   2014年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Methods in Molecular Biology  

    Frontal affinity chromatography (FAC) is a simple and effective method that is applicable to the analysis of interactions between glycans and glycan-recognition proteins, including lectins, with weak affinity ranging from 10<sup>-4</sup> to 10<sup>-6</sup> (M) in terms of dissociation constant (K <inf>d</inf>). Using conventional instruments, such as a high-performance liquid chromatography (HPLC) system equipped with pump, injector, (fluorescent) detector, and data recorder, the dissociation constants for weak glycan-based interactions can be easily determined with high throughput and accuracy. Notably, if the glycans are labeled with fluorescent dyes, only a small amount of glycans is required for the analysis. Fluorescent labeling of glycans is a common technique, and an increasing number of fluorescent-labeled glycans are commercially available. In this chapter, an advanced FAC method using fluorescent-labeled glycans is described. © 2014 Springer Science+Business Media New York.

    DOI: 10.1007/978-1-4939-1292-6_22

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  184. Comparison of analytical methods to detect polysialic acid. 査読有り

    Nishimura S, Hane M, Niimi Y, Miyata S, Kitajima K, Sato C

    Journal of Glycomics and Lipidomics   4 巻   頁: 113   2014年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  185. Polysialic acid: Biosynthesis, novel functions and applications. 査読有り

    Colley K, Kitajima K, Sato C

    Critical Reviews in Biochemistry and Molecular Biology     頁: 1-35   2014年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  186. NMR study into the mechanism of recognition of the degree of polymerization by oligo/polysialic acid antibodies. 査読有り

    Hanashima S, Sato C, Tanaka H, Takahashi T, Kitajima K, Yamaguchi Y.

    Bioorg. Med. Chem.   21 巻   頁: 6069-76   2013年10月

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  187. NMR study into the mechanism of recognition of the degree of polymerization by oligo/polysialic acid antibodies 査読有り

    Hanashima Shinya, Sato Chihiro, Tanaka Hiroshi, Takahashi Takashi, Kitajima Ken, Yamaguchi Yoshiki

    BIOORGANIC & MEDICINAL CHEMISTRY   21 巻 ( 19 ) 頁: 6069 - 6076   2013年10月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Bioorganic and Medicinal Chemistry  

    Oligo/polysialic acids consisting of consecutive α(2,8)-linkages on gangliosides and glycoproteins play a role in cell adhesion and differentiation events in a manner that is dependent on the degree of polymerization (DP). Anti-oligo/polysialic acid antibodies often have DP-dependent antigenic specificity, and such unique antibodies are often used in biological studies for the detection and differentiation of oligo/polysialic acids. However, molecular mechanisms remain unclear. We here use NMR techniques to analyze the binding epitopes of the anti-oligo/polysialic acid monoclonal antibodies (mAb) A2B5 and 12E3. The mAb A2B5, which has a preference for trisialic acid, recognizes sialic acid residues at the non-reducing terminus and those in nascent units. On the other hand, mAb 12E3, which prefers oligo/polysialic acids of more than six sugar units, recognizes inner sialic acid residues. In both structural complexes, the interresidue transferred NOE correlations are significantly different from those arising from analogs of the free states, indicating that the bound and free sugar conformations are distinct. The ability of the two mAbs to distinguish the chain lengths comes from different binding epitopes and possibly from the conformational differences in the oligo/polysialic acids. Information on the recognition modes is needed for the structural design of immunoreactive antigens for the development of high-affinity anti-polysialic acid antibodies and of related vaccines against pathogenic, polysialic acid-coated bacteria. © 2013 Elsevier Ltd. All rights reserved.

    DOI: 10.1016/j.bmc.2013.07.023

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  188. Polysialic acid

    Sato C.

    Sialobiology: Structure, Biosynthesis and Function. Sialic Acid Glycoconjugates in Health and Disease     頁: 33-75   2013年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.2174/9781608053865113010005

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  189. Disialic, oligosialic and polysialic acids: distribution, functions and related disease. 査読有り

    Sato C, Kitajima K

    Journal of biochemistry   154 巻 ( 2 ) 頁: 115 - 36   2013年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biochemistry  

    Sialic acids (Sia) are involved in many biological activities and frequently exist as monosialyl residues at the non-reducing terminal end of glycoconjugates. Occasionally, polymerized structures in the form of disialic acid (diSia), oligosialic acid (oligoSia) and polysialic acid (polySia) are also found in glycoconjugates. In particular, polySia, which is an evolutionarily conserved epitope from sea urchin to humans, is one of the most biologically important glycotopes in vertebrates. The biological functions of polySia, especially on neural cell adhesion molecules, have been well studied and an in-depth body of knowledge concerning polySia has been accumulated. However, considerably less attention has been paid to glycoproteins containing di-and oligoSia groups. However, advances in analytical methods for detecting oligo/polymerized structures have allowed the identification and characterization of an increasing number of glycoproteins containing di/oligo/polySia chains in nature. In addition, sophisticated genetic techniques have also helped to elucidate the underlying mechanisms of polySia-mediated activities. In this review, recent advances in the study of the chemical properties, distribution and functions of di-, oligo-and polySia residues on glycoproteins are described. © 2013 The Authors.

    DOI: 10.1093/jb/mvt057

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  190. Occurrence of free deaminoneuraminic acid (KDN)-containing complex-type N-glycans in human prostate cancers. 査読有り

    Yabu M, Korekane H, Takahashi H, Ohigashi H, Ishikawa O, Hatano K, Nonomura N, Sato C, Kitajima K, Miyamoto Y.

    Glycobiology   23 巻   頁: 634-642   2013年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  191. ポリシアル酸による神経機能の調節. 招待有り 査読有り

    佐藤ちひろ、北島健

    実験医学   31 巻   頁: 26--33   2013年

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    担当区分:筆頭著者   記述言語:日本語   掲載種別:研究論文(学術雑誌)  

  192. Disialic, oligosialic, and polysialic acids: Distribution, biological functions, and related disease. 招待有り 査読有り

    Sato C., Kitajima K.

    J Biochem (Tokyo).   154 巻   頁: 115-136   2013年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  193. Impact of structural aberrancy of polysialic acid and its synthetic enzyme ST8SIA2 in schizophrenia. 査読有り

    Sato C, Kitajima K.

    Front. Cell. Neurosci.   7 巻 ( 61 ) 頁: 1-11   2013年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  194. Crystal structure of anti-polysialic acid antibody single chain Fv fragment complexed with octasialic acid: insight into the binding preference for polysialic acid. 査読有り

    Nagae M, Ikeda A, Hane M, Hanashima S, Kitajima K, Sato C, Yamaguchi Y.

    J Biol Chem.   288 巻   頁: 33784-96   2013年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  195. Polysialic Acid

    Sato Chihiro

    SIALOBIOLOGY: BIOSYNTHESIS, STRUCTURE AND FUNCTION: SIALIC ACID GLYCOCONJUGATES IN HEALTH AND DISEASE     頁: 33-75   2013年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  196. ポリシアル酸による神経機能の調節. 招待有り 査読有り

    佐藤ちひろ, 北島健

    実験医学   31 巻   頁: 26--33   2013年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

  197. Crystal structure of anti-polysialic acid antibody single chain Fv fragment complexed with octasialic acid: insight into the binding preference for polysialic acid. 査読有り

    Nagae M, Ikeda A, Hane M, Hanashima S, Kitajima K, Sato C, Yamaguchi Y

    J Biol Chem.   288 巻   頁: 33784-96   2013年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  198. Occurrence of free deaminoneuraminic acid (KDN)-containing complex-type N-glycans in human prostate cancers. 査読有り

    Yabu M, Korekane H, Takahashi H, Ohigashi H, Ishikawa O, Hatano K, Nonomura N, Sato C, Kitajima K, Miyamoto Y

    Glycobiology   23 巻   頁: 634-642   2013年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  199. Impact of structural aberrancy of polysialic acid and its synthetic enzyme ST8SIA2 in schizophrenia. 査読有り

    Sato C, Kitajima K

    Front. Cell. Neurosci.   7 巻 ( 61 ) 頁: 1-11   2013年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  200. Pig sperm membrane microdomains contain a highly glycosylated 15-25-kDa wheat germ agglutinin-binding protein. 査読有り

    Kasekarn W, Kanazawa T, Hori K, Tsuchiyama T, Lian X, Garénaux E, Kongmanas K, Tanphaichitr N, Yasue H, Sato C, Kitajima K

    Biochemical and biophysical research communications   426 巻 ( 3 ) 頁: 356 - 62   2012年9月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical and Biophysical Research Communications  

    A highly glycosylated protein, which has unique, novel features in localization, structure, and potential function, is found in pig sperm, and named WGA-gp due to its high binding property with wheat germ agglutinin (WGA). WGA-gp is localized mainly in flagella and enriched in membrane microdomains or lipid rafts. It is not detected by ordinary protein staining methods due to a high content of both N- and O-glycans consisting of neutral monosaccharides. Interestingly, WGA-gp may be involved in intracellular Ca2+ regulation. Treatment of sperm with anti-WGA-gp antibody enhances the amplitude of Ca2+ oscillation without changing the basal intracellular Ca2+ concentrations. All these features of WGA-gp, except for different carbohydrate structures occupying most part of the molecules, are similar to those of flagellasialin in sea urchin sperm, which regulates the intracellular Ca2+ concentration. Presence of carbohydrate-enriched flagellar proteins involved in intracellular Ca2+ regulation may be a common feature among animal sperm. © 2012 Elsevier Inc.

    DOI: 10.1016/j.bbrc.2012.08.090

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  201. 26 ガングリオ系列ガングリオシド糖鎖のコンビナトリアル合成とその機能評価(口頭発表の部)

    田中 浩士, 西浦 祐二, 安田 優, 佐藤 ちひろ, 北島 健, 高橋 孝志

    天然有機化合物討論会講演要旨集   54 巻 ( 54 ) 頁: 151 - 156   2012年9月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:天然有機化合物討論会  

    Gangliosides are a family of glycolipids, which possess sialic acids that play important roles in biological events on cell surfaces. Ganglio-series gangliosides are composed of the tetrasaccharide, (Galβ(1,3)GalNAcβ(1,4)Galβ(1,4)Glc), which bears α(2,8) oligosialic acid units. Glycolipids that vary in number of sialic acids are known as the a-, b-, and c-series of gangliosides. Chemical synthesis of these di-/oligo-sialo-containing glycolipids and their derivatives would facilitate identification of their biological roles. However, the α(2,8) oligosialic acid unit and the compact and rigid 3,4 dibranched galactoside unit are difficult to prepare. Therefore, an effective method for the synthesis of a-, b-, and c-series of gangliosides is still needed. In this report, we describe combinatorial synthesis of ganglio-series ganglioside epitopes varying at the number of the sialic acids. The α(2,3) and α(2,8) sialylations were accomplished by use of 5N,4O-carbonyl and 7,8-O-isopropyliden, and 5N,4O-carbonyl- and 7,8-di-O-chloroacetyl-protected sialyl donors in good yields with excellent a-selectivity, respectively. The two sialyl donors enable synthesis of the di- and tri-sialylgalactosides by simple glycosylation and deprotection. We successfully prepared the ganglioside epitopes via direct construction of a compact, rigid, branched structure. We also reported on a competitive inhibiting activity of the soluble glycolipid library to binding solid-supported GD3 with Siglec-7.

    DOI: 10.24496/tennenyuki.54.0_151

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  202. Metabolism of vertebrate amino sugars with N-glycolyl groups: resistance of α2-8-linked N-glycolylneuraminic acid to enzymatic cleavage. 査読有り

    Davies LR, Pearce OM, Tessier MB, Assar S, Smutova V, Pajunen M, Sumida M, Sato C, Kitajima K, Finne J, Gagneux P, Pshezhetsky A, Woods R, Varki A

    The Journal of biological chemistry   287 巻 ( 34 ) 頁: 28917 - 28931   2012年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    The sialic acid (Sia)N-acetylneuraminic acid (Neu5Ac) and its hydroxylated derivative N-glycolylneuraminic acid (Neu5Gc) differ by one oxygen atom. CMP-Neu5Gc is synthesized from CMP-Neu5Ac, with Neu5Gc representing a highly variable fraction of total Sias in various tissues and among different species. The exception may be the brain, where Neu5Ac is abundant and Neu5Gc is reported to be rare. Here, we confirm this unusual pattern and its evolutionary conservation in additional samples from various species, concluding that brain Neu5Gc expression has been maintained at extremely low levels over hundreds of millions of years of vertebrate evolution. Most explanations for this pattern do not require maintaining neural Neu5Gc at such low levels. We hypothesized that resistance of α2-8-linked Neu5Gc to vertebrate sialidases is the detrimental effect requiring the relative absence of Neu5Gc from brain. This linkage is prominent in polysialic acid (polySia), a molecule with critical roles in vertebrate neural development.Weshow that Neu5Gc is incorporated into neural polySia and does not cause in vitro toxicity. Synthetic polymers of Neu5Ac and Neu5Gc showed that mammalian and bacterial sialidases are much less able to hydrolyze α2-8-linked Neu5Gc at the nonreducing terminus. Notably, this difference was not seen with acid-catalyzed hydrolysis of polySias. Molecular dynamics modeling indicates that differences in the three-dimensional conformation of terminal saccharides may partly explain reduced enzymatic activity. In keeping with this, polymers of N-propionylneuraminic acid are sensitive to sialidases. Resistance of Neu5Gc-containing polySia to sialidases provides a potential explanation for the rarity of Neu5Gc in the vertebrate brain. © 2012 by The American Society for Biochemistry and Molecular Biology, Inc.

    DOI: 10.1074/jbc.M112.365056

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  203. Structural and functional impairments of polySia-NCAM synthesized by a mutated polysialyltransferase of a schizophrenic patient. 査読有り

    Hane M, Sumida M, Kitajima K, Sato C.

    Pure Appl Chem   84 巻   頁: 1895-1906   2012年6月

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  204. Structural and functional impairments of polySia-NCAM synthesized by a mutated polysialyltransferase of a schizophrenic patient. 査読有り

    Hane M, Sumida M, Kitajima K, Sato C

    Pure Appl Chem   84 巻   頁: 1895-1906   2012年6月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  205. Sialidase NEU4 Hydrolyzes Polysialic Acids of Neural Cell Adhesion Molecules and Negatively Regulates Neurite Formation by Hippocampal Neurons 査読有り

    Takahashi Kohta, Mitoma Junya, Hosono Masahiro, Shiozaki Kazuhiro, Sato Chihiro, Yamaguchi Kazunori, Kitajima Ken, Higashi Hideyoshi, Nitta Kazuo, Shima Hiroshi, Miyagi Taeko

    JOURNAL OF BIOLOGICAL CHEMISTRY   287 巻 ( 18 ) 頁: 14816 - 14826   2012年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    Modulation of levels of polysialic acid (polySia), a sialic acid polymer, predominantly associated with the neural cell adhesion molecule (NCAM), influences neural functions, including synaptic plasticity, neurite growth, and cell migration. Biosynthesis of polySia depends on two polysialyltransferases ST8SiaII and ST8SiaIV in vertebrate. However, the enzyme involved in degradation of polySia in its physiological turnover remains uncertain. In the present study, we identified and characterized a murine sialidase NEU4 that catalytically degrades polySia. Murine NEU4, dominantly expressed in the brain, was found to efficiently hydrolyze oligoSia and polySia chains as substrates in sialidase in vitro assays, and also NCAM-Fc chimera as well as endogenous NCAM in tissue homogenates of postnatal mouse brain as assessed by immunoblotting with anti-polySia antibodies. Degradation of polySia by NEU4 was also evident in neuroblastoma Neuro2a cells that were co-transfected with Neu4 and ST8SiaIV genes. Furthermore, in mouse embryonic hippocampal primary neurons, the endogenously expressed NEU4 was found to decrease during the neuronal differentiation. Interestingly, GFP- or FLAG-tagged NEU4 was partially co-localized with polySia in neurites and significantly suppressed their outgrowth, whereas silencing of NEU4 showed the acceleration together with an increase in polySia expression. These results suggest that NEU4 is involved in regulation of neuronal function by polySia degradation in mammals. © 2012 by The American Society for Biochemistry and Molecular Biology, Inc.

    DOI: 10.1074/jbc.M111.324186

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  206. Sialidase NEU4 hydrolyzes polysialic acids of neural cell adhesion molecules and negatively regulates neurite formation by hippocampal neurons. 査読有り

    Takahashi K, Mitoma J, Hosono M, Shiozaki K, Sato C, Yamaguchi K, Kitajima K, Higashi H, Nitta K, Shima H, Miyagi T.

    J Biol Chem.   287 巻   頁: 14816-14826   2012年3月

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  207. Novel regulation of fibroblast growth factor 2 (FGF2)-mediated cell growth by polysialic acid. 査読有り

    Ono S, Hane M, Kitajima K, Sato C

    The Journal of biological chemistry   287 巻 ( 6 ) 頁: 3710 - 22   2012年2月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    Polysialic acid (polySia) is a unique polysaccharide that modifies neural cell adhesion molecule (NCAM) spatiotemporally. Recently, we demonstrated that polySia functions as a reservoir for several neurotrophic factors and neurotransmitters. Here, we showed the direct interaction between polySia and fibroblast growth factor-2 (FGF2) by native-PAGE, gel filtration, and surface plasmon resonance. The minimum chain length of polySia required for the interaction with FGF2 was 17. Compared with heparan sulfate, a well known glycosaminoglycan capable of forming a complex with FGF2, polySia formed a larger complex with distinct properties in facilitating oligomerization of FGF2, as well as in binding to FGF receptors. In polySia-NCAM-expressing NIH-3T3 cells, which were established by transfecting cells with either of the plasmids for the expression of the polysialyltransferases ST8SiaII/STX and ST8SiaIV/PST that can polysialylate NCAM, FGF2-stimulated cell growth, but not cell survival, was inhibited. Taken together, these results suggest that polySia-NCAM might be involved in the regulation of FGF2-FGF receptor signaling through the direct binding of FGF2 in a manner distinct from heparan sulfate. © 2012 by The American Society for Biochemistry and Molecular Biology, Inc.

    DOI: 10.1074/jbc.M111.276618

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  208. Sialome analysis of the cephalochordate Branchiostoma belcheri, a key organism for vertebrate evolution. 査読有り

    Guérardel Y, Chang LY, Fujita A, Coddeville B, Maes E, Sato C, Harduin-Lepers A, Kubokawa K, Kitajima K.

    Glycobiolgy     頁: in press   2012年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  209. Novel regulation of FGF2-mediated cell growth by polysialic acid. 査読有り

    Ono S, Hane M, Kitajima K, Sato C.

    J Biol Chem.     頁: 3710-22.   2012年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  210. Sialome analysis of the cephalochordate Branchiostoma belcheri, a key organism for vertebrate evolution. 査読有り

    Guérardel Y, Chang LY, Fujita A, Coddeville B, Maes E, Sato C, Harduin-Lepers A, Kubokawa K, Kitajima K

    Glycobiolgy     頁: in press   2012年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  211. Co-expression of two distinct polysialic acids, α2,8- and α2,9-linked polymers of N-acetylneuraminic acid, in distinct glycoproteins and glycolipids in sea urchin sperm. 査読有り

      21 巻   頁: 1596-1605   2011年12月

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  212. New function of polysialic acid and its involvement in neural activities

    Sato C.

    Seikagaku   83 巻 ( 3 ) 頁: 189-196   2011年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  213. Co-expression of two distinct polysialic acids, α2,8- and α2,9-linked polymers of N-acetylneuraminic acid, in distinct glycoproteins and glycolipids in sea urchin sperm. 査読有り

    Miyata S, Yamakawa N, Toriyama M, Sato C, Kitajima K

    Glycobiology   21 巻   頁: 1596-1605   2011年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  214. The Roles of Carbohydrate Binding in Cell Adhesion and Inflammation 査読有り

    Kitajima K., Sato C.

    Carbohydrate Recognition: Biological Problems, Methods, and Applications     頁: 33 - 63   2011年7月

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    記述言語:英語   掲載種別:論文集(書籍)内論文   出版者・発行元:Carbohydrate Recognition: Biological Problems, Methods, and Applications  

    DOI: 10.1002/9781118017586.ch2

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  215. ポリシアル酸の新機能と神経形成維持機構

    佐藤 ちひろ, 北島 健

    生化學   83 巻 ( 3 ) 頁: 189-196   2011年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  216. ポリシアル酸の新機能と神経形成維持機構 査読有り

    佐藤ちひろ, 北島 健

    生化学   83 巻   頁: 189-196   2011年3月

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    担当区分:筆頭著者   記述言語:日本語   掲載種別:研究論文(学術雑誌)  

  217. [New function of polysialic acid and its involvement in neural activities].

    Sato C, Kitajima K

    Seikagaku. The Journal of Japanese Biochemical Society   83 巻 ( 3 ) 頁: 189-96   2011年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  218. Structural and functional impairments of polysialic acid by a mutated polysialyltransferase found in schizophrenia 査読有り

    Isomura, R., Kitajima, K., and Sato, C.

    J. Biol. Chem.   286 巻   頁: 21535-21545   2011年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  219. New functions of polysialic acid and its relationship to schizophrenia 査読有り

    Sato C and Kitajima K

      23 巻   頁: 221-238   2011年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  220. Human KDN (deaminated neuraminic acid) and its elevated expression in cancer cells: mechanism and significance. 査読有り

    Inoue S, Kitajima K, Sato C, Go S

    Advances in experimental medicine and biology   705 巻   頁: 669 - 78   2011年

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    記述言語:英語   掲載種別:研究論文(国際会議プロシーディングス)   出版者・発行元:Advances in Experimental Medicine and Biology  

    Sialic acids are a family of nine-carbon carboxylated sugars having a nonulosonate skeletal structure (Fig. 35.1). This structure is uniquely different from that of other sugar units of animal glycans. The most popular sialic acid is N-acetylneuraminic acid (Neu5Ac), which is universally found on cell surface glycocalyx and in secreted glycoproteins of vertebrates and some invertebrates. Sialic acids have low acid-base dissociation constants and give a negative charge on the cell surface under a wide range of physiological pH. In nature, more than 50 kinds of sialic acids are known. Nearly all of them are derived from Neu5Ac by a substitution on the hydroxyl groups (e.g., O-acetyl-Neu5Ac) and/or a hydroxylation of the N-acetyl group (e.g., N-glycolylneuraminic acid, Neu5Gc). Each modified sialic acid has properties different from those of Neu5Ac and is believed to contribute to specific physiological functions. In animal cells, sialic acids are most frequently the terminal sugars of cell surface glycolipids and glycoproteins, and any change that occurs on sialic acids can considerably influence the biological properties of a cell. © 2011 Springer Science+Business Media, LLC.

    DOI: 10.1007/978-1-4419-7877-6_35

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  221. Mechanism regulating Ca2+-dependent mechanosensory behaviour in sea urchin spermatozoa. 査読有り

    Kambara Y, Shiba K, Yoshida M, Sato C, Kitajima K, Shingyoji C

    Cell structure and function   36 巻 ( 1 ) 頁: 69 - 82   2011年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Cell Structure and Function  

    Flagellar movement of the sea urchin sperm is regulated by intracellular Ca2+. Flagellasialin, a polysialic acid-containing glycoprotein, as well as other membrane proteins seems responsible for the Ca2+ control. To elucidate the mechanism of Ca2+ dynamics underlying flagellar movement, we analysed the sperm's mechanosensory behavioural responses by using microtechniques. In sea water containing 10 mM Ca2+, the sperm swim in circular paths. When a mechanical stimulus was applied to the sperm head with a glass microstylus, the sperm showed a series of flagellar responses, consisting of a stoppage of beating (quiescence) and a recovery of swimming in a straight path, followed by swimming in a circular path again; as the result the sperm avoided the obstacle. Ca2+-imaging with Fluo-4 showed that the intracellular Ca2+ was high in the quiescence and gradually decreased after that. The effects of blockers and antibodies against candidate components revealed that the Ca2+ influx was induced by Ca2+ channels and the Ca2+ efflux was induced by a flagellasialin-related Ca2+- efflux system, plasma membrane Ca2+-ATPases and the K+-dependent Na+/Ca2+ exchanger. The results show that the Ca2+-dependent mechanosensory behaviour of the sea urchin sperm is regulated by organized functioning of the membrane environment including the plasma membrane proteins and flagellasialin. © 2011 by Japan Society for Cell Biology.

    DOI: 10.1247/csf.10020

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  222. Mechanism Regulating Ca2+-dependent Mechanosensory Behaviour in Sea Urchin Spermatozoa

    Kambara Yuka, Shiba Kogiku, Yoshida Manabu, Sato Chihiro, Kitajima Ken, Shingyoji Chikako

    CELL STRUCTURE AND FUNCTION   36 巻 ( 1 ) 頁: 69-82   2011年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  223. Structural and functional impairments of polysialic acid by a mutated polysialyltransferase found in schizophrenia 査読有り

    Isomura, R, Kitajima, K, Sato, C

    J. Biol. Chem.   286 巻   頁: 21535-21545   2011年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  224. New functions of polysialic acid and its relationship to schizophrenia 査読有り

    Sato C, Kitajima K

    TIGG   23 巻   頁: 221-238   2011年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  225. Developmental stage-dependent expression of an alpha2,8-trisialic acid unit on glycoproteins in mouse brain. 査読有り

    Inoko E, Nishiura Y, Tanaka H, Takahashi T, Furukawa K, Kitajima K, Sato C

    Glycobiology   20 巻 ( 7 ) 頁: 916 - 28   2010年7月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    The monoclonal antibody mAb.A2B5 is a marker for the detection of oligodendrocyte progenitor cells that differentiate into type-2 astrocytes and oligodendrocytes. It is also a useful antibody for separating these cells from other lineage populations. The epitope of this antibody is considered to be the gangliosides GT3 and GQ1c. In this study, we sought to define more precisely the structure of the epitope. Accordingly, we chemically synthesized defined oligosialic acid structures linked to phosphatidylethanolamine and bovine serum albumin and used these to determine the antigenic specificity. mAb.A2B5 recognized the Neu5Acα2→8-Neu5Acα2→8Neu5Acα → structure on both glycolipids and glycoproteins. We then examined whether the mAb. A2B5 epitope exists on glycoproteins in developing mouse brains. Western blot analyses revealed the expression of four glycoproteins reactive with the mAb.A2B5, and their expression was dependent on the stage of neural development. All the immunoreactivity in these glycoproteins with mAb.A2B5 disappeared after sialidase treatment and were resistant to chloroform/methanol extraction. These epitopes were also detected in brain homogenates from both GD3 synthetase-null and GD3/GD2 synthetase double null mice. These findings show that the α 2,8- trisialic acid (triSia) unit recognized by mAb.A2B5 resides not only on gangliosides but also on glycoproteins in developing mouse brain. We postulate that the triSia structure on glycoproteins may be involved in oligodendrocyte differentiation, similar to the case with the α 2,8-triSia structure on gangliosides. Real time polymerase chain reaction analysis of the developmental expression of all known ST8Sia genes, which are responsible for the biosynthesis of α 2,8- linked Sia residues, showed that ST8Sia III gene expression correlated with expression of the triSia epitope. We suggest that ST8Sia III is the principal sialyltransferase responsible for synthesis of the α 2,8-triSia units on glycoproteins. © The Author 2010. Published by Oxford University Press. All rights reserved.

    DOI: 10.1093/glycob/cwq049

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  226. 糖鎖と統合失調症 招待有り

    佐藤ちひろ

    生体の科学   61 巻   頁: 160-166   2010年

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    担当区分:筆頭著者   記述言語:日本語   掲載種別:研究論文(学術雑誌)  

  227. IgG2 dominancy and carbohydrate recognition specificity of C3H/He mouse antibodies directed to cross-reactive carbohydrate determinants (CCDs) bearing beta-(1,2)-xylose and alpha-(1,3)-fucose. 査読有り

    Hino S, Umeda F, Inumaru S, Aoki N, Sato, C., Okajima T, Nadano D, Matsuda T.

    Immunol Lett   133 巻   頁: 28-34   2010年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  228. Survival signals of hepatic stellate cells in liver regeneration are regulated by glycosylation changes in rat vitronectin, especially decreased sialylation. 査読有り

    Sano K, Miyamoto Y, Kawasaki N, Hashii N, Itoh S, Murase M, Date K, Yokoyama M, Sato, C., Kitajima K, Ogawa H.

    J Biol Chem   285 巻   頁: 17301-17309   2010年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  229. Extensive enrichment of N-glycolylneuraminic acid in extracellular sialoglycoproteins abundantly synthesized and secreted by human cancer cells. 査読有り

    Inoue, S., Sato, C. and Kitajima, K

    Glycobiology   20 巻   頁: 752-762   2010年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  230. Developmental stage-dependent expression of an α2,8-trisialic acid unit on glycoproteins in mouse brain. 査読有り

    Inoko, E., Nishiura, Y., Tanaka, H., Takahashi, T., Furukawa, K., Kitajima, K., and Sato, C.

    Glycobiology   20 巻   頁: 916-928   2010年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  231. Survival signals of hepatic stellate cells in liver regeneration are regulated by glycosylation changes in rat vitronectin, especially decreased sialylation. 査読有り

    Sano K, Miyamoto Y, Kawasaki N, Hashii N, Itoh S, Murase M, Date K, Yokoyama M, Sato, C, Kitajima K, Ogawa H

    J Biol Chem   285 巻   頁: 17301-17309   2010年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  232. 糖鎖と統合失調症 招待有り

    佐藤ちひろ

    生体の科学   61 巻   頁: 160-166   2010年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

  233. Extensive enrichment of N-glycolylneuraminic acid in extracellular sialoglycoproteins abundantly synthesized and secreted by human cancer cells. 査読有り

    Inoue, S, Sato, C, Kitajima, K

    Glycobiology   20 巻   頁: 752-762   2010年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  234. IgG2 dominancy and carbohydrate recognition specificity of C3H/He mouse antibodies directed to cross-reactive carbohydrate determinants (CCDs) bearing beta-(1,2)-xylose and alpha-(1,3)-fucose. 査読有り

    Hino S, Umeda F, Inumaru S, Aoki N, Sato, C, Okajima T, Nadano D, Matsuda T

    Immunol Lett   133 巻   頁: 28-34   2010年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  235. Periodate-resistant carbohydrate epitopes recognized by IgG and IgE antibodies from some of the immunized mice and patients with allergy. 査読有り

    Hino S, Matsubara T, Urisu A, Aoki N, Sato C, Okajima T, Nadano D, Matsuda T

    Biochemical and biophysical research communications   380 巻 ( 3 ) 頁: 632 - 7   2009年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biochemical and Biophysical Research Communications  

    The β(1,2)-xylose- and/or α(1,3)-fucose-containing cross-reactive carbohydrate determinants (CCDs) are present in various plant and insect N-glycans, and have been attracted as potential antigens in IgE-mediated allergies and immunologically undesired post-translational products on some recombinant therapeutic proteins. By using ELISA and immunoblotting, CCDs-specific IgG and IgE antibodies from some, but not all, of mice and humans were found to fully retain their binding activity after a typical periodate-treatment to CCDs, which did cause the CCDs' antigenic activity to those from the other mice and rabbits to disappear almost completely. Furthermore, the mouse IgE recognizing the periodate-resistant CCDs induced the CCDs/IgE-dependent degranulation of rat basophilic RBL-2H3 cells. These findings indicate that in some cases CCDs include those dependent of the core trisaccharide more strongly than the terminal xylose and fucose, which might have been screened out in the CCDs analyses based on the loss of antibody-binding by the periodate-treatment. © 2009 Elsevier Inc. All rights reserved.

    DOI: 10.1016/j.bbrc.2009.01.138

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  236. Membrane microdomains from early gastrula embryos of medaka, Oryzias latipes are a plat form of E-cadherin and carbohydrate-mediated cell-cell interactions during epiboly 査読有り

    Adachi T., Sato, C., Kishi, Y., Totani, K., Murata, T., Usui, T., and Kitajima, K

    Glycoconjugate J.   26 巻   頁: 285-299   2009年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  237. Complex formation of a brain-derived neurotrophic factor and glycosaminoglycans. 査読有り

    Kanato, Y., Kitajima, K. and Sato, C.

    Biosci. Biotech. Biosci.   12 巻   頁: 1044-1053   2009年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  238. Developmental regulation of oligosialylation in zebrafish. 査読有り

    Chang LY, Harduin-Lepers A, Kitajima K, Sato C, Huang CJ, Khoo KH, Guérardel Y.

    Glycoconjugate J.   26 巻   頁: 247-61   2009年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  239. Complex formation of a brain-derived neurotrophic factor and glycosaminoglycans. 査読有り

    Kanato, Y, Kitajima, K, Sato, C

    Biosci. Biotech. Biosci.   12 巻   頁: 1044-1053   2009年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  240. Membrane microdomains from early gastrula embryos of medaka, Oryzias latipes are a plat form of E-cadherin and carbohydrate-mediated cell-cell interactions during epiboly 査読有り

    Adachi T, Sato, C, Kishi, Y, Totani, K, Murata, T, Usui, T, Kitajima, K

    Glycoconjugate J.   26 巻   頁: 285-299   2009年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  241. Developmental regulation of oligosialylation in zebrafish. 査読有り

    Chang LY, Harduin-Lepers A, Kitajima K, Sato C, Huang CJ, Khoo KH, Guérardel Y

    Glycoconjugate J.   26 巻   頁: 247-61   2009年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  242. [Regulation of signal transduction by polysialic acid]. 査読有り

    Sato C, Kitajima K

    Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme   53 巻 ( 12 Suppl ) 頁: 1577 - 1583   2008年9月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

    PubMed

  243. Direct binding of polysialic acid to a brain-derived neurotrophic factor depends on the degree of polymerization 査読有り

    Kanato, Y, Kitajima, K., and Sato, C.

    Glycobiology   12 巻   頁: 1044-1053   2008年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  244. ポリシアル酸構造による細胞シグナルの調節機構 招待有り

    佐藤ちひろ、北島健

    蛋白質核酸酵素   53 巻 ( 1577-1583 )   2008年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

  245. Direct binding of polysialic acid to a brain-derived neurotrophic factor depends on the degree of polymerization 査読有り

    Kanato, Y, Kitajima, K, Sato, C

    Glycobiology   12 巻   頁: 1044-1053   2008年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  246. Glycobiology of polysialic acids on sea urchin gametes

    Miyata Shinji, Sato Chihiro, Kitajima Ken

    TRENDS IN GLYCOSCIENCE AND GLYCOTECHNOLOGY   19 巻 ( 106 ) 頁: 85-98   2007年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  247. Identification of an inflammation-inducible serum protein recognized by anti-disialic acid antibodies as carbonic anhydrase II. 査読有り

    Yasukawa Z, Sato C, Kitajima K

    Journal of biochemistry   141 巻 ( 3 ) 頁: 429 - 41   2007年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biochemistry  

    Acute-phase proteins are an important marker of inflammation and sometimes have a role in the general defense response towards tissue injury. In the present study, we identified a 32-kDa protein that was immunoreactive with monoclonal antibody 2-4B (mAb.2-4B), which is specific to di/oligoNeu5Gc structures, and that behaved as an acute-phase protein following stimulation with either turpentine oil or lipopolysaccharides. The 32-kDa protein was identified as carbonic anhydrase II (CA-II), based on matrix-assisted laser desorption/ionization time-of-flight mass spectrometry analyses of the purified protein. Mouse and human CA-II was immunoreactive and immunoprecipitated with mAb.2-4B, but contained no sialic acid. In addition to mAb.2-4B, the mAb. S2-566 an antibody specific for diNeu5Ac-containing glycans, recognized the CA-II, whereas an anti-oligo/polysialic acid antibody did not. These results indicate that a part of the CA-II protein structure mimics the disialic acid structure recognized by the monoclonal antibodies. This is the first report that CA-II circulates in the serum following inflammation. © 2007 The Japanese Biochemical Society.

    DOI: 10.1093/jb/mvm047

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  248. Heterocomplex formation and cell-surface accumulation of hen's serum zona pellucida B1 (ZPB1) with ZPC expressed by a mammalian cell line (COS-7): A possible initiating step of egg-envelope matrix construction

    Okumura Hiroki, Aoki Naohito, Sato Chihiro, Nadano Daita, Matsuda Tsukasa

    BIOLOGY OF REPRODUCTION   76 巻 ( 1 ) 頁: 9-18   2007年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  249. Heterocomplex formation and cell-surface accumulation of hen's serum zona pellucida B1 (ZPB1)with ZPC expressed by a mammalian cell line (COS-7): a possible initiating step of egg-envelope matrix construction. 査読有り

    Okumura H, Aoki N, Sato C, Nadano D, Matsuda T

    Biology of reproduction   76 巻 ( 1 ) 頁: 9 - 18   2007年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Biology of Reproduction  

    The egg envelope, referred to as zona pellucida (ZP) in mammalian eggs, is a fibrous and noncollagenous extracellular matrix surrounding vertebrate eggs, and composed of three to four homologous glycoproteins with a common ZP domain. In birds, a liver-derived ZP glycoprotein (ZP1/ZPB1) is transported through the bloodstream to ovarian follicles and joins the egg-envelope matrix construction together with the other ZP glycoproteins, such as ZPC and ZPD/ZPX2, both secreted from follicular granulosa cells. We report here that, through its ZP domain, ZPB1 specifically associates with ZPC, which might lead to the construction of egg-envelope matrix. The ZPB1 in laying hen's serum specifically bound to ZPC, but not to ZPX2, separated by SDS-PAGE and blotted on a membrane. Hemagglutinin (HA)-tagged ZPC expressed in a mammalian cell line (COS-7) cells was processed and secreted as a mature-form into the culture medium. From the culture supernatant of ZPC-expressing transfectants cultured in the presence of ZPB1, both ZPB1 and ZPC were recovered as heterocomplexes by immunoprecipitation using either anti-HA or anti-ZPB1 antibody. Interestingly, a monoclonal antibody, 8E1, which immunoprecipitated free ZPB1, did not immunoprecipitate the ZPB1-ZPC heterocomplexes. An 8E1 epitope was mapped on a C-terminal region of the ZP domain in a ZPB1 molecule by identifying an 8E1-positive peptide using mass spectroscopy. Furthermore, by laser scanning confocal microscopy, ZPB1 and ZPC were observed to colocalize on the surface of ZPC-expressing transfectants cultured in the presence of ZPB1, whereas almost no ZPC was detected on the surface of the transfectants cultured in the absence of ZPB1. Taken together, these results suggest that ZPB1 transported into ovarian follicles encounters and associates with ZPC secreted from granulosa cells, resulting in the formation of heterocomplexes around an oocyte. In addition, it appears that such ZPB1-ZPC complexes accumulated on the oocyte surface act as a scaffold for subsequent matrix construction events including ZPX2 association. © 2007 by the Society for the Study of Reproduction, Inc.

    DOI: 10.1095/biolreprod.106.056267

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    PubMed

  250. Complex formation of 70-kDa heat shock protein with acidic glycolipids and phospholipids. 査読有り

    Harada Y, Sato C, Kitajima K.

    Biochem Biophys Res Commun.   353 巻   頁: 655-660   2007年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  251. The rainbow trout CMP-sialic acid synthetase utilises a nuclear localization signal different from that identified in the mouse enzyme. 査読有り

    Tiralongo J, Fujita A, Sato C, Kitajima K, Lehmann F, Oschlies M, Gerardy-Schahn R, Munster-Kuhnel AK.

    Glycobiology   17 巻   頁: 945-954   2007年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  252. Identification of an inflammation-inducible serum protein recognized by anti-disialic acid antibodies as carbonic anhydrase II. 査読有り

    Yasukawa, Z., Sato, C., and Kitajima, K.

    J Biochem.   141 巻   頁: 429-441   2007年

     詳細を見る

    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Acute phase proteins are an important marker of inflammation and sometimes have a role in the general defense response towards tissue injury. In the present study, we identified a 32 kDa protein that was immunoreactive with monoclonal antibody 2-4B (mAb.2-4B), which is specific to di/oligoNeu5Gc structures, and that behaved as an acute phase protein following stimulation with either turpentine oil or lipopolysaccharides. The 32 kDa protein was identified as carbonic anhydrase II (CA-II), based on matrix-assisted laser desorption/ionization time-of-flight mass spectrometry analyses of the purified protein. Mouse and human CA-II was immunoreactive and immunoprecipitated with mAb.2-4B, but contained no sialic acid. In addition to mAb.2-4B, the mAb. S2-566 an antibody specific for diNeu5Ac-containing glycans, recognized the CA-II, whereas an anti-oligo/polysialic acid antibody did not. These results indicate that a part of the CA-II protein structure mimics the disialic acid structure recognized by the monoclonal antibodies. This is the first report that CA-II circulates in the serum following inflammation.

  253. シアル酸の構造多様性とその生物学的意義. 招待有り

    北島 健、郷 慎司、藤田 明子、佐藤ちひろ

    細胞工学   26 巻   頁: 629-634   2007年

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    記述言語:日本語  

  254. Membrane microdomain formation is crucial in epiboly during gastrulation of medaka. 査読有り

    Adachi, T., Sato, C., and Kitajima, K.

    Biochem. Biophys. Res. Commun.   355 巻   頁: 174-180   2007年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  255. Development of sensitive chemical and immunochemical methods for detecting sulfated sialic acids and their application to glycoconjugates from sea urchin sperm and eggs 査読有り

    Yamakawa, N., Sato C., Miyata, S., Maehashi, E., Toriyama, T., Sato, N., Furuhata, K., and Kitajima. K.

    Biochimie   89 巻   頁: 1396-1408   2007年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  256. Glycobiology of polysialic acids on sea urchin gametes. 招待有り 査読有り

    Miyata, S., Sato, C., and Kitajima, K.

    Trends Glycosci. Glycotech.   19 巻   頁: 83-95   2007年

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    記述言語:英語  

  257. Hypoxia-enhanced expression of free deaminoneuraminic acid in human cancer cells. 査読有り

    Go, S., Sato, C., Yin, J., Kannagi, R., and Kitajima, K.

    Biochem. Biophys. Res. Commun.   357 巻   頁: 537-542.   2007年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  258. Identification of the nuclear export signals that regulate the intracellular localization of the mouse CMP-sialic acid synthetase. 査読有り

    Fujita, A, Sato C, and Kitajima, K.

    Biochem. Biophys. Res. Commun.   355 巻   頁: 174-180   2007年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  259. The rainbow trout CMP-sialic acid synthetase utilises a nuclear localization signal different from that identified in the mouse enzyme. 査読有り

    Tiralongo J, Fujita A, Sato C, Kitajima K, Lehmann F, Oschlies M, Gerardy-Schahn R, Munster-Kuhnel AK

    Glycobiology   17 巻   頁: 945-954   2007年

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  260. シアル酸の構造多様性とその生物学的意義. 招待有り

    北島 健, 郷 慎司, 藤田 明子, 佐藤ちひろ

    細胞工学   26 巻   頁: 629-634   2007年

     詳細を見る

    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

  261. Complex formation of 70-kDa heat shock protein with acidic glycolipids and phospholipids. 査読有り

    Harada Y, Sato C, Kitajima K

    Biochem Biophys Res Commun.   353 巻   頁: 655-660   2007年

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  262. Membrane microdomain formation is crucial in epiboly during gastrulation of medaka. 査読有り

    Adachi, T, Sato, C, Kitajima, K

    Biochem. Biophys. Res. Commun.   355 巻   頁: 174-180   2007年

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  263. Identification of the nuclear export signals that regulate the intracellular localization of the mouse CMP-sialic acid synthetase. 査読有り

    Fujita, A, Sato C, Kitajima, K

    Biochem. Biophys. Res. Commun.   355 巻   頁: 174-180   2007年

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  264. Hypoxia-enhanced expression of free deaminoneuraminic acid in human cancer cells. 査読有り

    Go, S, Sato, C, Yin, J, Kannagi, R, Kitajima, K

    Biochem. Biophys. Res. Commun.   357 巻   頁: 537-542.   2007年

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  265. Glycobiology of polysialic acids on sea urchin gametes. 招待有り 査読有り

    Miyata, S, Sato, C, Kitajima, K

    Trends Glycosci. Glycotech.   19 巻   頁: 83-95   2007年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  266. Development of sensitive chemical and immunochemical methods for detecting sulfated sialic acids and their application to glycoconjugates from sea urchin sperm and eggs 査読有り

    Yamakawa, N, Sato C, Miyata, S, Maehashi, E, Toriyama, T, Sato, N, Furuhata, K, Kitajima. K

    Biochimie   89 巻   頁: 1396-1408   2007年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  267. AMPAR removal underlies Abeta-induced synaptic depression and dendritic spine loss.

    Hsieh H, Boehm J, Sato C, Iwatsubo T, Tomita T, Sisodia S, Malinow R

    Neuron   52 巻 ( 5 ) 頁: 831-43   2006年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1016/j.neuron.2006.10.035

    PubMed

  268. Expression and functional importance of the carbohydrate antigen 3D11 in early embryo of medaka, Oryzias latipes

    Kitajima Ken, Hara Hiroaki, Adachi Tomoko, Sato Chihiro

    ZOOLOGICAL SCIENCE   23 巻 ( 12 ) 頁: 1175-1175   2006年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  269. Flagellasialin: a novel sulfated alpha2,9-linked polysialic acid glycoprotein of sea urchin sperm flagella. 査読有り

    Miyata S, Sato C, Kumita H, Toriyama M, Vacquier VD, Kitajima K

    Glycobiology   16 巻 ( 12 ) 頁: 1229 - 41   2006年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    A novel α2,9-linked polysialic acid (polySia)-containing glycoprotein of sea urchin sperm flagella was identified and named "flagellasialin." Flagellasialin from Hemicentrotus pulcherrimus shows a diverse relative molecular mass on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) of 40-80 kDa. Flagellasialin is a 96-amino acid, threonine-rich, heavily O-glycosylated (80-90% by weight) glycoprotein with a single transmembrane segment at its C-terminus and no apparent cytosolic domain. Of 12 extracellular Thr residues, eight are O-glycosylated and three are nonglycosylated. Flagellasialin is highly expressed in the testis but cannot be detected in the ovary. The amino acid sequences of flagellasialin from three sea urchin species (H. pulcherrimus, Strongylocentrotus purpuratus, and Strongylocentrotus franciscanus) are identical, but some species differences exist in the three core glycan structures to which the sulfated α2,9-linked polyNeu5Ac chain is linked. Finally, the treatment of sperm with a specific antibody against the α2,9-linked polyNeu5Ac structure results in the elevation of intracellular Ca2+ and inhibition of sperm motility and fertilization, implicating flagellasialin as a regulator of these critical processes. © 2006 Oxford University Press.

    DOI: 10.1093/glycob/cwl036

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  270. Identification of disialic acid-containing glycoproteins in mouse serum: a novel modification of immunoglobulin light chains, vitronectin, and plasminogen. 査読有り

    Yasukawa Z, Sato C, Sano K, Ogawa H, Kitajima K

    Glycobiology   16 巻 ( 7 ) 頁: 651 - 65   2006年7月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    Serum glycoproteins are involved in various biologic activities, such as the removal of exogenous antigens, fibrinolysis, and metal transport. Some of them are also useful markers of inflammation and disease. Although the amount of sialic acid increases following inflammation, little attention has been paid to the presence of linkage-specific epitopes in serum, especially the α2,8-linkage. In a previous study, we demonstrated that four components in mouse serum contain α2,8-linked disialic acid (diSia), based on immunoreactivity with monoclonal antibody 2-4B, which is specific to N-glycolylneuraminic acid (Neu5Gc)α2→(8Neu5Gcα2→)n-1, n ≥ 2 [Yasukawa et al., (2005) Glycobiology, 15, 827-837]. In this study, we purified three components, 30-, 70-, and 120-kDa gp, and identified them as an immunoglobulin (Ig) light chain, vitronectin, and plasminogen, respectively, using matrix-assisted laser desorption/ionization time-of-flight mass spectroscopy analyses. Modifications of these proteins with α2,8-linked diSia were chemically confirmed by fluorometric C7/C9 analyses and mild acid hydrolysates-fluorometric anion-exchange chromatography analyses. We also demonstrated that the IgG, IgM, and IgE light chains are commonly modified with α2,8-linked diSia. In addition, both mouse and rat vitronectin contained diSia, and the amount of disialylation in vitronectin dramatically decreased after hepatectomy. These results indicate that a novel diSia modification of serum glycoproteins is biologically important for immunologic events and fibrinolysis. © 2006 Oxford University Press.

    DOI: 10.1093/glycob/cwj112

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  271. Hypoxic culture induces expression of Sialin, a sialic acid transporter, and cancer-associated gangliosides containing non-human sialic acid on human cancer cells. , 査読有り

    Yin, J., Hashimoto, A., Izawa, M., Miyazaki, K., Chen G-Y., Takematsu, H., Kozutsumi, Y., Suzuki, A., Furuhata, K., Cheng, F.-L. Lin, C.-H., Sato, C., Kitajima, K., and Kannagi, R.

    Cancer Res.   66 巻   頁: 2937-2945   2006年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  272. Flagellasialin: a novel sulfated alpha2,9-linked polysialic acid glycoprotein of sea urchin sperm flagella. 査読有り

    Miyata S, Sato C, Kumita H, Toriyama M, Vacquier VD, Kitajima K.

    Glycobiology   16 巻   頁: 1229-12241   2006年

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    A novel α2,9-linked polysialic acid-containing glycoprotein of sea urchin sperm flagella was previously identified and named “flagellasialin". Flagellasialin from Hemicentrotus pulcherrimus shows a diverse relative molecular mass on SDS-PAGE of 40-80 kDa. Its glycan structures were determined as HSO3→8Neu5Acα2→9(Neu5Acα2→9)n-2Neu5Acα2→6GalNAcα1→Thr (n, averaging 15) [Miyata et al. (2004) Glycobiology, 14, 827-840]. In this study, we purified flagellasialin, and cloned its cDNA. Flagellasialin is a 96-amino acid, threonine-rich, heavily O-glycosylated (80-90% by weight) glycoprotein with a single transmembrane segment at its C-terminus and no apparent cytosolic domain. Of 12 extracellular Thr residues, eight are O-glycosylated and three are non-glycosylated. Flagellasialin is highly expressed in testis, but cannot be detected in ovary. The amino acid sequences of flagellasialin from three sea urchin species (H. pulcherrimus, Strongylocentrotus purpuratus and S. franciscanus) are identical, but some species differences exist in the three core glycan structures to which the sulfated α2,9-linked polyNeu5Ac chain is linked. Finally, a specific antibody against the α2,9-linked polyNeu5Ac structure inhibits sperm motility and reduces fertilization, implicating flagellasialin as a regulator of these critical processes.

  273. *Identification of disialic acid-containing glycoproteins in mouse serum. 査読有り

    Yasukawa, Z., Sato, C., Sano, K., Ogawa, H. and Kitajima, K.

    Glycobiology   15 巻   頁: 827-837   2006年

     詳細を見る

    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Serum glycoproteins are involved in various biological activities such as removal of exogenous antigen, fibrinolysis, transport of metal. They are also useful markers of inflammation and diseases. Although it is known that the amount of sialic acid increases after inflammation, little attention has been paid to the presence of linkage specific epitope in serum,especially, the α2,8-linkage. In the previous study, we demonstrated that four components in mouse serum contain the α2,8-linked disialic acid, based on the immunoreactivity with mAb.2-4B that is specific to Neu5Gcα2→(8Neu5Gcα2→)n-1, n≥2 (Yasukawa, Z. et al. (2005) Glycobiology 15, 827-837). In this study, we purified three components, 30kDa-gp, 70kDa-gp, and 120kDa-gp and identified as the light chain of immunoglobulins, vitronectin, and plasminogen, respectively, using MALDI-TOF MS analyses. The modifications of these proteins with the α2,8-linked disialic acid was chemically confirmed by fluorometric C7/C9 analyses and acid hydrolysates-DMB methods. We also showed that the light chains of IgG, IgM and IgE are commonly modified with the α2,8-linked disialic acid. In addition, not only mouse vitronectin but also rat vitronectin was also modified with disialic acid and the amount of disialylation on vitronectin decreased after hepatectomy. These results indicate that disialic acid-modification on serum glycoprotein has some biological meanings in immunological events and fibrinolysis.

  274. Involvement of the alpha2,8-polysialyltransferases II/STX and IV/PST in the biosynthesis of polysialic acid chains on the O-linked glycoproteins in rainbow trout ovary. 査読有り

    Asahina S, Sato C, Matsuno M, Matsuda T, Colley K, Kitajima K. Asahina S, Sato C, Matsuno M, Matsuda T, Colley K, Kitajima K.

    J Biochem.   140 巻   頁: 687-701   2006年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  275. Oral ingestion of mannose alters the expression level of deaminoneuraminic acid (KDN) in mouse organs. 査読有り

    Go, S., Sato, C., and Kitajima, K.

    Glycoconjugate J.   23 巻   頁: 411-421   2006年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  276. Weaning-induced expression of a milk-fat globule protein, MFG-E8, in mouse mammary glands, as demonstrated by the analyses of its mRNA, protein and phosphatidylserine-binding activity. 査読有り

    Nakatani H, Aoki N, Nakagawa Y, Jin-No S, Aoyama K, Oshima K, Ohira S, Sato C, Nadano D, Matsuda T.

    Biochem J.   395 巻   頁: 21-30   2006年

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  277. Weaning-induced expression of a milk-fat globule protein, MFG-E8, in mouse mammary glands, as demonstrated by the analyses of its mRNA, protein and phosphatidylserine-binding activity. 査読有り

    Nakatani H, Aoki N, Nakagawa Y, Jin-No S, Aoyama K, Oshima K, Ohira S, Sato C, Nadano D, Matsuda T

    Biochem J.   395 巻   頁: 21-30   2006年

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  278. Hypoxic culture induces expression of Sialin, a sialic acid transporter, and cancer-associated gangliosides containing non-human sialic acid on human cancer cells. , 査読有り

    Yin, J, Hashimoto, A, Izawa, M, Miyazaki, K, Chen G-Y, Takematsu, H, Kozutsumi, Y, Suzuki, A, Furuhata, K, Cheng, F.-L. Lin, C.-H, Sato, C, Kitajima, K, Kannagi, R

    Cancer Res.   66 巻   頁: 2937-2945   2006年

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  279. Oral ingestion of mannose alters the expression level of deaminoneuraminic acid (KDN) in mouse organs. 査読有り

    Go, S, Sato, C, Kitajima, K

    Glycoconjugate J.   23 巻   頁: 411-421   2006年

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  280. Involvement of the alpha2,8-polysialyltransferases II/STX and IV/PST in the biosynthesis of polysialic acid chains on the O-linked glycoproteins in rainbow trout ovary. 査読有り

    Asahina S, Sato C, Matsuno M, Matsuda T, Colley K, Kitajima, K, Asahina S, Sato C, Matsuno M, Matsuda T, Colley K, Kitajima K

    J Biochem.   140 巻   頁: 687-701   2006年

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  281. Inflammation-dependent changes in alpha2,3-, alpha2,6-, and alpha2,8-sialic acid glycotopes on serum glycoproteins in mice. 査読有り

    Yasukawa Z, Sato C, Kitajima K

    Glycobiology   15 巻 ( 9 ) 頁: 827 - 37   2005年9月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    The expression of acute-phase serum proteins increases in response to inflammatory stimuli. Most of these proteins are glycoproteins that often contain sialic acids (Sia). It is unknown, however, how the expression of Sia in these glycoproteins changes during inflammation. This study demonstrates changes in the α2,3-, α2,6-, and α2,8-Sia glycotopes on serum glycoproteins in response to turpentine oil-induced inflammation, based on lectin- and immunoblot analyses by using sialyl linkage-specific lectins, Maackia amurensis for the α2,3-Sia glycotope and Sambucus sieboldiana for the α2,6-Sia glycotopes, and monoclonal antibody 2-4B (mAb.2-4B) recognizing the di- and oligomers of the α2,8-Neu5Gc residue. There was an increase in a limited number of sialoglycoproteins containing the α2,3-, α2,6-, or α2,8-Sia glycotopes. Reverse transcription-polymerase chain reaction (RT-PCR) analysis of the expression profiles of mRNAs for the known sialyltransferases in mouse liver during inflammation indicated the up-regulated expression of β-galactoside α2,3-sialyltransferases (ST3Gal I and ST3Gal III) and β-N-acetylgalactosaminide α2,6-sialyltransferase (ST6GalNAc VI) as well as β-galactoside α2,6-sialyltransferase (ST6Gal I) mRNAs. Notably, ST3Gal I and III and ST6GalNAc VI are involved in the synthesis of the α2,3- and α2,6-Sia glycotopes on O-glycan chains and possibly on gangliosides, whereas ST6Gal I is specific for N-glycan chains. These results provide evidence for the inflammation-induced expression of sialyl glycotopes in serum glycoproteins. We demonstrated that inflammation significantly increased the expression of an unknown 32-kDa glycoprotein containing the α2,8-Sia glycotope. The mechanism for the increase in glycoprotein in inflamed mouse serum remains to be examined, as mRNA expression for all of the α2,8-sialyltransferases (ST8Sia I-VI) was unchanged during inflammation. © The Author 2005. Published by Oxford University Press. All right reserved.

    DOI: 10.1093/glycob/cwi068

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  282. Crystallization and preliminary X-ray analysis of mitochondrial presequence receptor Tom20 in complexes with a presequence from aldehyde dehydrogenase

    Igura M, Ose T, Obita T, Sato C, Maenaka K, Endo T, Kohda D

    ACTA CRYSTALLOGRAPHICA SECTION F-STRUCTURAL BIOLOGY COMMUNICATIONS   61 巻 ( 5 ) 頁: 514-517   2005年5月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1107/S1744309105011577

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  283. Distal myopathy with rimmed vacuoles - Impaired O-glycan formation in muscular glycoproteins

    Tajima Y, Uyama E, Go S, Sato C, Tao N, Kotani M, Hino H, Suzuki A, Sanai Y, Kitajima K, Sakuraba H

    AMERICAN JOURNAL OF PATHOLOGY   166 巻 ( 4 ) 頁: 1121-1130   2005年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  284. Distal myopathy with rimmed vacuoles: impaired O-glycan formation in muscular glycoproteins. 査読有り

    Tajima Y, Uyama E, Go S, Sato C, Tao N, Kotani M, Hino H, Suzuki A, Sanai Y, Kitajima K, Sakuraba H

    The American journal of pathology   166 巻 ( 4 ) 頁: 1121 - 30   2005年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:American Journal of Pathology  

    Distal myopathy with rimmed vacuoles (DMRV), is an autosomal recessive disorder with early adult onset, displays distal dominant muscular involvement and is characterized by the presence of numerous rimmed vacuoles in the affected muscle fibers. The pathophysiology of DMRV has not been clarified yet, although the responsible gene was identified as that encoding UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase involved hi the biosynthesis of sialic acids. To identify defective carbohydrate moieties of muscular glycoproteins from DMRV patients, frozen skeletal muscle sections from seven patients with DMRV, as well as normal and pathological controls, were treated with or without sialidase or N-glycosidase F followed by lectin staining and lectin blotting analysis. The sialic acid contents of the O-glycans in the skeletal muscle specimens from the DMRV patients were also measured. We found that Arachis hypogaea agglutinin (PNA) lectin reacted strongly with sarcolemmal glycoproteins in the DMRV patients but not with those in control subjects. α-Dystroglycan from the DMRV patients strongly associated with PNA lectin, although that from controls did not. The sialic acid level of the O-glycans in the DMRV muscular glycoproteins with molecular weights of 30 to 200 kd was reduced to 60 to 80% of the control level. The results show that impaired sialyl O-glycan formation in muscular glycoproteins, including α-dystroglycan, occurs in DMRV.

    DOI: 10.1016/S0002-9440(10)62332-2

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  285. Differentiation of noncancerous tissue and cancer lesions by apparent diffusion coefficient values in transition and peripheral zones of the prostate

    Sato C, Naganawa S, Nakamura T, Kumada H, Miura S, Takizawa O, Ishigaki T

    JOURNAL OF MAGNETIC RESONANCE IMAGING   21 巻 ( 3 ) 頁: 258-262   2005年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    DOI: 10.1002/jmri.20251

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  286. Development of a simple and efficient method for assaying cytidine monophosphate sialic acid synthetase activity using an enzymatic reduced nicotinamide adenine dinucleotide/oxidized nicotinamide adenine dinucleotide converting system. 査読有り

    Fujita A, Sato C, Münster-Kühnel AK, Gerardy-Schahn R, Kitajima K

    Analytical biochemistry   337 巻 ( 1 ) 頁: 12 - 21   2005年2月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Analytical Biochemistry  

    A new reliable method to assay the activity of cytidine monophosphate sialic acid (CMP-Sia) synthetase (CSS) has been developed. The activation of sialic acids (Sia) to CMP-Sia is a prerequisite for the de novo synthesis of sialoglycoconjugates. In vertebrates, CSS has been cloned from human, mouse, and rainbow trout, and the crystal structure has been resolved for the mouse enzyme. The mouse and rainbow trout enzyme have been compared with respect to substrate specificity, demonstrating that the mouse enzyme exhibits a pronounced specificity for N-acetylneuraminic acid (Neu5Ac), while the rainbow trout CSS is equally active with either of three Sia species, Neu5Ac, N-glycolylneuraminic acid (Neu5Gc), and deaminoneuraminic acid (KDN). However, molecular details that explain the pronounced substrate specificities are unknown. Understanding the catalytic mechanisms of these enzymes is of major importance, since CSSs play crucial roles in cellular sialylation patterns and thus are potential drug targets in a number of pathophysiological situations. The availability of the cDNAs and the obtained structural data enable rational approaches; however, these efforts are limited by the lack of a reliable high-throughput assay system. Here we describe a new assay system that allows product quantification in a reduced nicotinamide adenine dinucleotide (NADH)-dependent color reaction. The activation reaction catalyzed by CSS, CTP + Sia → CMP-Sia + pyrophosphate, was evaluated by a consumption of Sia, which corresponds to that of NADH on the following two successive reactions: (i) Sia → pyruvate + ManNAc (or Man), catalyzed by a sialic acid lyase (SAL), and (ii) pyruvate + NADH → lactate + oxidized nicotinamide adenine dinucleotide (NAD +), catalyzed by a lactate dehydrogenase (LDH). Consumption of NADH can be photometrically monitored on a microtiter plate reader for a number of test samples at the same time. Furthermore, based on the quantification of CSS used in the SAL/LDH assay, relative activities toward Sia derivatives have been obtained. The preference of mouse CSS toward Neu5Ac and the ability of the rainbow trout enzyme to activate both KDN and Neu5Ac were confirmed. Thus, this simple and time-saving method is suitable for a systematic comparison of enzyme activity of structurally mutated enzymes based on the relative specific activity. © 2004 Elsevier Inc. All rights reserved.

    DOI: 10.1016/j.ab.2004.10.033

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  287. Distal Myopathy with Rimmed Vaculoes. 査読有り

    Tajima, Y., Uyama, E., Go, S., Sato, C., Tao, N., Kotani, M., Hino, H., Suzuki, A.,Sanai, Y., Kitajima, K., and Sakuraba, H.

    Am. J. Pathol.   166 巻   頁: 1121-1128   2005年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  288. Inflammation-dependent changes in α2,3-, α2,6-, and α2,8-sialic acid glycotopes on serum glycoproteins in mouse. 査読有り

    Yasukawa, Z., Sato, C., and Kitajima, K.

    Glycobiology   15 巻   頁: 827-837   2005年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  289. Cell growth stimulating activity of the peptides derived from cortical alveolus glycoproteins of fish egg (hyosophorin)

    Maeda Eri, Sato Chihiro, Kitajima Ken

    ZOOLOGICAL SCIENCE   21 巻 ( 12 ) 頁: 1292-1292   2004年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  290. Studies on chemical properties of cyclic sialic acid using their synthetic S- and O-glycosides as model compounds

    Iwata S, Sato C, Ando H, Kiso M, Kannagi R, Kitajima K

    GLYCOBIOLOGY   14 巻 ( 11 ) 頁: 1163-1163   2004年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  291. A major flagellum sialoglycoprotein in sea urchin sperm contains a novel polysialic acid, an alpha2,9-linked poly-N-acetylneuraminic acid chain, capped by an 8-O-sulfated sialic acid residue. 査読有り

    Miyata S, Sato C, Kitamura S, Toriyama M, Kitajima K

    Glycobiology   14 巻 ( 9 ) 頁: 827 - 40   2004年9月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Glycobiology  

    A new type of polysialic acid (polySia) structure was demonstrated to occur in a major unknown sialoglycoprotein with a diverse molecular mass of 40-80 kDa in sea urchin sperm. The polySia-containing glycan structure was determined to be HSO3→8Neu5Acα2→9(Neu5Acα2→9 n-2 Neu5Acα2→6GalNAcα1→Ser/Thr (n, on average 15), based on carbohydrate analysis of the sialoglycopeptide obtained by an exhaustive protease digestion of whole sperm, fluorometric anion-exchange high-performance liquid chromatography, and methylation analysis. The sulfate group was predominantly localized to the nonreducing terminus of the polySia chain. This is the first example of an α2,9-linked polySia structure in animal sperm. The polySia-containing sialoglycoprotein was present in sperm flagellum but not in the head. Furthermore, this sialoglycoprotein localized in the sperm lipid raft, which contains an enriched ganglioside (Neu5Acα 2→8Neu5Acα2→6GlcCer), a receptor for sperm-activating peptide (speract), and its associated guanylate cyclase. © Oxford University Press 2004; all rights reserved.

    DOI: 10.1093/glycob/cwh100

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  292. Chain length diversity of sialic acids and its biological significance

    Sato C

    TRENDS IN GLYCOSCIENCE AND GLYCOTECHNOLOGY   16 巻 ( 91 ) 頁: 331-344   2004年9月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  293. 母乳中に発見された新規ポリシアロ糖タンパク質 : CD36がユニークな糖鎖修飾を受けていることが明らかに

    佐藤 ちひろ

    化学と生物   42 巻 ( 1 ) 頁: 12-14   2004年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  294. alpha-C-Mannosyltryptophan is not recognized by conventional mannose-binding lectins 査読有り

    T.Nishikawa, S. Kajii, C. Sato, Z. Yasukawa, K. Kitajima, and M. Isobe

    Bioorg Med Chem.     頁: 2343-2348   2004年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  295. A major flagellum sialoglycoprotein in sea urchin sperm contains a novel polysialic acid, an α2,9-linked poly-N-acetylneuraminic acid chain, capped by an 8-O-sulfated sialic acid residue 査読有り

    S. Miyata, C. Sato, S. Kitamura, S. Toriyama, and K. Kitajima,

    Glycobiology   14 巻   頁: 827-840   2004年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    A new type of polysialic acid (polySia) structure was demonstrated to occur in a major unknown sialoglycoprotein with a diverse molecular mass of 40-80 kDa in sea urchin sperm. The polySia-containing glycan structure was determined to be HSO3→8Neu5Acα2→9(Neu5Acα2→9)n-2 Neu5Acα2 →6GalNAcα1→Ser/Thr (n, on average 15), based on carbohydrate analysis of the sialoglycopeptide obtained by an exhaustive protease digestion of whole sperm, fluorometric anion-exchange high performance liquid chromatography, and methylation analysis. role in sperm activation and migration in the extracellular coats at fertilization, like polySia on neural cell adhesion molecule acts as a regulator of neural cell functions.

  296. Specificity of human trans-sialidase as probed with gangliosides. 査読有り

    Nikonova, E. Y., Tertov, V. V., Sato, C., Kitajima, K., and Bovin, N. V.

    Bioorg. Med. Chem. Lett.   14 巻   頁: 5161-5164   2004年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  297. A newly identified zona pellucida glycoprotein, ZPD and dimeric ZP1 of chicken egg envelope are involved in sperm activation on sperm-egg interaction 査読有り

    H. Okumura, Y. Kohno, Y. Iwata, H. Mori, N. Aoki, C. Sato, K. Kitajima, D. Nadano, and T. Matsuda

    Biochem. J.   383 巻   頁: 1-9   2004年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  298. Development of a simple and efficient method for assaying the CMP-sialic acid synthetase activity using an enzymatic NADH/NAD+ converting system 査読有り

    A. Fujita, C. Sato, A.-K. Münster-Kühnel, R. Gerardy-Schahn, and K. Kitajima

    Anal. Biochem.   337 巻   頁: 12-21   2004年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  299. *Chain length diversity of sialic acids and its biological significance (Review) 招待有り 査読有り

    C. Sato

    Trends Glycosci. Glycotechnol   16 巻   頁: 331-344   2004年

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    担当区分:筆頭著者   記述言語:英語  

  300. Developmental Expression of a Sialyltransferase Responsible for Sialylation of Cortical Alveolus Glycoprotein During Oogenesis in Rainbow Trout (Oncorhynchus mykiss) 査読有り

    S. Asahina, C.Sato, and K. Kitajima

    J. Biochem.   136 巻   頁: 189-198   2004年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  301. ジシアル酸・オリゴシアル酸・ポリシアル酸の生物学的機能 招待有り

    佐藤ちひろ

      3 巻   頁: 40-47   2004年

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    担当区分:筆頭著者   記述言語:日本語  

  302. Specificity of human trans-sialidase as probed with gangliosides. 査読有り

    Nikonova, E. Y, Tertov, V. V, Sato, C, Kitajima, K, Bovin, N. V

    Bioorg. Med. Chem. Lett.   14 巻   頁: 5161-5164   2004年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  303. ジシアル酸・オリゴシアル酸・ポリシアル酸の生物学的機能 招待有り

    佐藤ちひろ

    Functional Glycomics   3 巻   頁: 40-47   2004年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

  304. alpha-C-Mannosyltryptophan is not recognized by conventional mannose-binding lectins 査読有り

    T.Nishikawa, S. Kajii, C. Sato, Z. Yasukawa, K. Kitajima, M. Isobe

    Bioorg Med Chem.     頁: 2343-2348   2004年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  305. A newly identified zona pellucida glycoprotein, ZPD and dimeric ZP1 of chicken egg envelope are involved in sperm activation on sperm-egg interaction 査読有り

    H. Okumura, Y. Kohno, Y. Iwata, H. Mori, N. Aoki, C. Sato, K. Kitajima, D. Nadano, T. Matsuda

    Biochem. J.   383 巻   頁: 1-9   2004年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  306. *Chain length diversity of sialic acids and its biological significance (Review) 招待有り 査読有り

    C. Sato

    Trends Glycosci. Glycotechnol   16 巻   頁: 331-344   2004年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  307. Developmental Expression of a Sialyltransferase Responsible for Sialylation of Cortical Alveolus Glycoprotein During Oogenesis in Rainbow Trout (Oncorhynchus mykiss) 査読有り

    S. Asahina, C.Sato, K. Kitajima

    J. Biochem.   136 巻   頁: 189-198   2004年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  308. ポリシアル酸の鎖長多様性とタンパク質機能

    佐藤 ちひろ

    生化學   75 巻 ( 12 ) 頁: 1526-1530   2003年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  309. Frequent occurrence and biological significance of degree of polymerization in sialic acid

    Sato C.

    Seikagaku. The Journal of Japanese Biochemical Society   75 巻 ( 12 ) 頁: 1526-1530   2003年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  310. Frequent occurrence and biological significance of degree of polymerization in sialic acid

    Sato C

    SEIKAGAKU   75 巻 ( 12 ) 頁: 1526-1530   2003年12月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  311. Discovery of two new polysialoglycoproteins in human and sea urchin. Linkage and length diversities of polysialic acid in animal glycoproteins

    Kitajima K, Yabe U, Miyata S, Sato CH

    GLYCOBIOLOGY   13 巻 ( 11 ) 頁: 844-844   2003年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

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  312. Identification of the sea urchin 350-kDa sperm-binding protein as a new sialic acid-binding lectin that belongs to the heat shock protein 110 family: implication of its binding to gangliosides in sperm lipid rafts in fertilization. 査読有り

    Maehashi E, Sato C, Ohta K, Harada Y, Matsuda T, Hirohashi N, Lennarz WJ, Kitajima K

    The Journal of biological chemistry   278 巻 ( 43 ) 頁: 42050 - 7   2003年10月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    The 350-kDa sperm-binding protein (SBP), a species-specific sperm-binding protein, is localized in the vitelline layer of sea urchin eggs. In this study, we have shown for the first time that sperm gangliosides are ligands for the intact glycosylated SBP. Using recombinant fragments of the SBP, the N-terminal heat shock protein 110-like domain was shown to be responsible for the binding. The intact SBP could bind various gangliosides, and the binding was sialidase-sensitive and inhibited by sialyllactose, thus indicating that it is the sialic acid-binding protein. Calcium and magnesium ions were not required but they did enhance the binding activity of SBP. The observation that bacterially expressed recombinant SBP and the sialidase-treated intact glycosylated SBP lost divalent cation-dependent enhancement of binding activity suggests that the sialylated carbohydrate moieties of the SBP may be involved in this property. Furthermore, the SBP was shown to bind sperm lipid rafts, in which gangliosides are enriched, and this binding was lost upon sialidase treatment of the lipid rafts. Finally, liposomes containing the ganglioside specifically inhibited fertilization. Taken together, these results allow us to identify SBP as a member of a new class of sialic acid-binding lectin belonging to the Hsp110 family, and indicate that SBP may be involved in interaction of sperm with the vitelline layer of the egg.

    DOI: 10.1074/jbc.M307493200

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  313. [Oligosialic acid: a common carbohydrate epitope in glycoproteins and glycolipids]. 査読有り

    Sato C, Kitajima K

    Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme   48 巻 ( 12 ) 頁: 1730 - 1736   2003年9月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

    PubMed

  314. Polysialic acid in human milk. CD36 is a new member of mammalian polysialic acid-containing glycoprotein. 査読有り

    Yabe U, Sato C, Matsuda T, Kitajima K

    The Journal of biological chemistry   278 巻 ( 16 ) 頁: 13875 - 80   2003年4月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:Journal of Biological Chemistry  

    The neural cell adhesion molecule and the voltage-sensitive sodium channel α-subunit are the only two molecules in mammals known to be modified by α-2,8-linked polysialic acid (polySia). We found a new polySia-containing glycoprotein in human milk and identified it as CD36, a member of the B class of the scavenger receptor superfamily. The polysia-containing glycan chain(s) were removed by alkaline treatment but not by peptide: N-glycanase F digestion, indicating that milk CD36 contained polysia on O-linked glycan chain(s). Polysialylation of CD36 occurs not only in human milk but also in mouse milk. However, CD36 in human platelets is not polysialylated. PolySia CD36 is secreted in milk at any lactation stage and reaches peak level at 1 month after parturition. Thus, it is suggested that polySia of milk CD36 is significant for neonatal development in terms of protection and nutrition.

    DOI: 10.1074/jbc.M300458200

    Web of Science

    Scopus

    PubMed

  315. Polysialic acid in human milk 査読有り

    U. Yabe, C. Sato, T. Matsuda, and K. Kitajima

    J. Biol. Chem.   278 巻   頁: 13875-13880   2003年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  316. ポリシアル酸の鎖長多様性とタンパク質機能 招待有り 査読有り

    佐藤ちひろ

    生化学   75 巻   頁: 1526-1530   2003年

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    担当区分:筆頭著者   記述言語:日本語  

  317. 糖タンパク質と糖脂質の共通糖鎖オリゴシアル酸の普遍的存在とその意義 招待有り

    佐藤ちひろ、北島 健

    蛋白質・核酸・酵素   48 巻   頁: 1730-1736   2003年

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    担当区分:筆頭著者   記述言語:日本語  

  318. Identification of the sea urchin 350 kDa sperm binding protein as a new sialic acid-binding lectin that belongs to the heat shock protein 110 family. 査読有り

    E. Maehashi, C. Sato, K. Ohta, Y. Harada, T., Matsuda, N. Hirohashi, W. J. Lennarz, and K. Kitajima

    J. Biol. Chem.   278 巻   頁: 42050-42057   2003年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  319. ポリシアル酸の鎖長多様性とタンパク質機能 招待有り 査読有り

    佐藤ちひろ

    生化学   75 巻   頁: 1526-1530   2003年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

  320. 糖タンパク質と糖脂質の共通糖鎖オリゴシアル酸の普遍的存在とその意義 招待有り

    佐藤ちひろ, 北島 健

    蛋白質・核酸・酵素   48 巻   頁: 1730-1736   2003年

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)  

  321. マウス炎症時における血清糖タンパク質上のシアル酸構造の変動

    安川 然太, 佐藤 ちひろ, 松田 幹, 北島 健

    生化学   74 巻 ( 11 ) 頁: 1389 - 1389   2002年11月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:(公社)日本生化学会  

  322. 炎症誘導マウスにおけるジ及びオリゴシアル酸含有血清糖タンパク質の解析

    安川 然太, 佐藤 ちひろ, 北島 健

    生化学   74 巻 ( 8 ) 頁: 726 - 726   2002年8月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:(公社)日本生化学会  

  323. *Neuronal differentiation-dependent expression of the disialic acid epitope on CD166 and its involvement in neurite formation in Neuro2A cells. 査読有り

    C. Sato, T. Matsuda, and K. Kitajima

    J. Biol. Chem.   277 巻   頁: 45299-45303   2002年

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  324. *Neuronal differentiation-dependent expression of the disialic acid epitope on CD166 and its involvement in neurite formation in Neuro2A cells. 査読有り

    C. Sato, T. Matsuda, K. Kitajima

    J. Biol. Chem.   277 巻   頁: 45299-45303   2002年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  325. Occurrence of oligosialic acids on integrin alpha(5) subunit and their involvement in cell adhesion to fibronectin

    Nadanaka S, Sato C, Kitajima K, Katagiri K, Irie S, Yamagata T

    JOURNAL OF BIOLOGICAL CHEMISTRY   276 巻 ( 36 ) 頁: 33657-33664   2001年9月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  326. Identification and adipocyte differentiation-dependent expression of the unique disialic acid residue in an adipose tissue-specific glycoprotein, adipo Q

    Sato C, Yasukawa Z, Honda N, Matsuda T, Kitajima K

    JOURNAL OF BIOLOGICAL CHEMISTRY   276 巻 ( 31 ) 頁: 28849-28856   2001年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  327. 脂肪細胞特異的血清タンパク質adipo Qのジ/オリゴシアル酸含有糖鎖の構造

    安川 然太, 佐藤 ちひろ, 本田 直輝, 松田 幹, 北島 健

    生化学   73 巻 ( 8 ) 頁: 695 - 695   2001年8月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:(公社)日本生化学会  

  328. Occurrence of oligosialic acids on integrin a5 subunit and their involvement in cell adhesion to fibronectin. 査読有り

    "S. Nadanaka, C. Sato, K. Kitajima, K. Katagiri, S. Irie, and T. Yamagata 276 (2001) in press"

    J. Biol. Chem.   276 巻   頁: 33657-33664   2001年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  329. Identification and adipocyte differentiation-dependent expression of the unique disialic acid residues in an adipose tissue specific glycoprotein, adipo Q 査読有り

    "C. Sato, Z. Yasukawa, N. Honda, T. Matsuda, and K. Kitajima"

    J. Biol. Chem.   276 巻   頁: 28849-28856   2001年1月

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  330. Identification and adipocyte differentiation-dependent expression of the unique disialic acid residues in an adipose tissue specific glycoprotein, adipo Q 査読有り

    C. Sato, Z. Yasukawa, N. Honda, T. Matsuda, K. Kitajima

    J. Biol. Chem.   276 巻   頁: 28849-28856   2001年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    0021-9258

  331. Occurrence of oligosialic acids on integrin a5 subunit and their involvement in cell adhesion to fibronectin. 査読有り

    S. Nadanaka, C. Sato, K. Kitajima, K. Katagiri, S. Irie, T. Yamagat, in press

    J. Biol. Chem.   276 巻   頁: 33657-33664   2001年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    0021-9258

  332. ウシ胎児血清糖タンパク質adipo Qの精製とそのジシアル酸含有糖鎖の同定

    安川 然太, 佐藤 ちひろ, 本田 直輝, 松田 幹, 北島 健

    生化学   72 巻 ( 8 ) 頁: 719 - 719   2000年8月

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    記述言語:日本語   掲載種別:研究論文(学術雑誌)   出版者・発行元:(公社)日本生化学会  

  333. Frequent occurrence of pre-existing alpha 2 -> 8-linked disialic and oligosialic acids with chain lengths up to 7 Sia residues in mammalian brain glycoproteins - Prevalence revealed by highly sensitive chemical methods and anti-di-, oligo-, and poly-Sia antibodies specific for defined chain lengths

    Sato C, Fukuoka H, Ohta K, Matsuda T, Koshino R, Kobayashi K, Troy FA, Kitajima K

    JOURNAL OF BIOLOGICAL CHEMISTRY   275 巻 ( 20 ) 頁: 15422-15431   2000年5月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  334. Co-localization of receptor and transducer proteins in the glycosphingolipid-enriched, low density, detergent-insoluble membrane fraction of sea urchin sperm. 査読有り

    "K. Ohta,, C. Sato, T. Matsuda, M. Toriyama, V. D. Vacquier, W. J.Lennarz, and K. Kitajima"

    Glycoconjugate J.   17 巻   頁: 205-214   2000年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  335. *Frequent occurrence of pre-existing alpha2,8-linked disialic and oligosialic acids with chain lengths up to 7 Sia residues in mammalian brain glycoproteins. 査読有り

    "C. Sato, H. Fukuoka, K. Ohta, T. Matsuda, R. Koshino, K. Kobayashi, F. A. Troy II, and K. Kitajima"

    J. Biol. Chem.   275 (20) 巻   頁: 15422-15431   2000年1月

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  336. *Frequent occurrence of pre-existing alpha2,8-linked disialic and oligosialic acids with chain lengths up to 7 Sia residues in mammalian brain glycoproteins. 査読有り

    C. Sato, H. Fukuoka, K. Ohta, T. Matsuda, R. Koshino, K. Kobayashi, F. A. Troy II, K. Kitajima

    J. Biol. Chem.   275 (20) 巻   頁: 15422-15431   2000年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    0021-9258

  337. Co-localization of receptor and transducer proteins in the glycosphingolipid-enriched, low density, detergent-insoluble membrane fraction of sea urchin sperm. 査読有り

    K. Ohta, C. Sato, T. Matsuda, M. Toriyama, V. D. Vacquier, W. J.Lennarz, K. Kitajima

    Glycoconjugate J.   17 巻   頁: 205-214   2000年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    0282-0080

  338. Co-localization of receptor and transducer proteins in the glycosphingolipid-enriched, low density, detergent-insoluble membrane fraction of sea urchin sperm

    Ohta K, Sato C, Matsuda T, Toriyama M, Vacquier VD, Lennarz WJ, Kitajima K

    GLYCOCONJUGATE JOURNAL   17 巻 ( 3-4 ) 頁: 205-214   2000年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  339. Lipid raft on gametic cells as a functional domain for sperm-egg interaction coupled with signal transduction 査読有り

    K Ohta, C Sato, T Matsuda, M Toriyama, VD Vacquier, N Hirohashi, WJ Lennarz, K Kitajima

    ZYGOTE   8 巻   頁: S63 - S63   2000年

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    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:CAMBRIDGE UNIV PRESS  

    Web of Science

  340. Glycobiology of di- and oligosialyl glycotopes

    Sato C, Kitajima K

    TRENDS IN GLYCOSCIENCE AND GLYCOTECHNOLOGY   11 巻 ( 62 ) 頁: 371-390   1999年11月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  341. Cholesterol-dependent localization of NAP-22 on a neuronal membrane microdomain (Raft)

    Maekawa S, Sato C, Kitajima K, Funatsu N, Kumanogoh H, Sokawa Y

    JOURNAL OF BIOLOGICAL CHEMISTRY   274 巻 ( 30 ) 頁: 21369-21374   1999年7月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  342. Isolation and characterization of low density detergent-insoluble membrane (LD-DIM) fraction from sea urchin sperm

    Ohta K, Sato C, Matsuda T, Toriyama M, Lennarz WJ, Kitajima K

    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS   258 巻 ( 3 ) 頁: 616-623   1999年5月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  343. A 42-kDa glycoprotein from chicken egg-envelope, an avian homolog of the ZPC family glycoproteins in mammalian zona pellucida - Its first identification, cDNA cloning and granulosa cell-specific expression

    Takeuchi Y, Nishimura K, Aoki N, Adachi T, Sato C, Kitajima K, Matsuda T

    EUROPEAN JOURNAL OF BIOCHEMISTRY   260 巻 ( 3 ) 頁: 736-742   1999年3月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  344. Fluorescent-assisted detection of oligosialyl units in glycoconjugates

    Sato C, Inoue S, Matsuda T, Kitajima K

    ANALYTICAL BIOCHEMISTRY   266 巻 ( 1 ) 頁: 102-109   1999年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  345. A 42-kDa glycoprotein from chicken egg-envelope, an avian homolog of the ZPC family glycoproteins in mammalian zona pellucida. Its first identification, cDNA cloning and granulosa cell-specific expression. 査読有り

    "T. Takeuchi, K. Nishimura, N. Aoki, T. Adachi, C. Sato, K. Kitajima, and T. Matsuda"

    Eur. J. Biochem.   273 巻   頁: 21526-21530   1999年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  346. Cholesterol-dependent localization of NAP-22 on a neuronal membrane microdomain (Raft). 査読有り

    "S. Maekawa, C. Sato, K. Kitajima, H. Kumanogoh, N. Funatsu, and Y. Sokawa"

    J. Biol. Chem.   274 巻   頁: 21369-21374   1999年1月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  347. Isolation and characterization of low density detergent-insoluble membrane (LD-DIM) fraction from sea urchin sperm. 査読有り

    "K. Ohta, C. Sato, T. Matsuda, M. Toriyama, W. J. Lennarz, and K. Kitajima"

    Biochem. Biophys. Res. Commun.   258 巻   頁: 616-623   1999年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  348. Fluorescent-assisted detection of oligosialyl units in glycoconjugates. 査読有り

    "C. Sato, S. Inoue, T. Matsuda, and K. Kitajima"

    Anal. Biochem.   267 巻   頁: 102-109   1999年1月

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  349. Glycobiology of di and oligosialyl glycotopes. 招待有り 査読有り

    "C. Sato, and K. Kitajima"

    Trends Glycosci. Glycotechnol.   11 巻   頁: 371-390   1999年1月

     詳細を見る

    担当区分:筆頭著者   記述言語:英語  

  350. A 42-kDa glycoprotein from chicken egg-envelope, an avian homolog of the ZPC family glycoproteins in mammalian zona pellucida. Its first identification, cDNA cloning and granulosa cell-specific expression. 査読有り

    T. Takeuchi, K. Nishimura, N. Aoki, T. Adachi, C. Sato, K. Kitajima, T. Matsuda

    Eur. J. Biochem.   273 巻   頁: 21526-21530   1999年1月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    0014-2956

  351. Cholesterol-dependent localization of NAP-22 on a neuronal membrane microdomain (Raft). 査読有り

    S. Maekawa, C. Sato, K. Kitajima, H. Kumanogoh, N. Funatsu, Y. Sokawa

    J. Biol. Chem.   274 巻   頁: 21369-21374   1999年1月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    0021-9258

  352. Fluorescent-assisted detection of oligosialyl units in glycoconjugates. 査読有り

    C. Sato, S. Inoue, T. Matsuda, K. Kitajima

    Anal. Biochem.   267 巻   頁: 102-109   1999年1月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    0003-2697

  353. Isolation and characterization of low density detergent-insoluble membrane (LD-DIM) fraction from sea urchin sperm. 査読有り

    K. Ohta, C. Sato, T. Matsuda, M. Toriyama, W. J. Lennarz, K. Kitajima

    Biochem. Biophys. Res. Commun.   258 巻   頁: 616-623   1999年1月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    0006-291X

  354. Glycobiology of di and oligosialyl glycotopes. 招待有り 査読有り

    C. Sato, K. Kitajima

    Trends Glycosci. Glycotechnol.   11 巻   頁: 371-390   1999年1月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  355. Development of a highly sensitive chemical method for detecting alpha 2 -> 8-linked oligo/polysialic acid residues in glycoproteins blotted on the membrane

    Sato C, Inoue S, Matsuda T, Kitajima K

    ANALYTICAL BIOCHEMISTRY   261 巻 ( 2 ) 頁: 191-197   1998年8月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  356. Identification of oligo-N-glycolylneuraminic acid residues in mammal-derived glycoproteins by a newly developed immunochemical reagent and biochemical methods

    Sato C, Kitajima K, Inoue S, Inoue Y

    JOURNAL OF BIOLOGICAL CHEMISTRY   273 巻 ( 5 ) 頁: 2575-2582   1998年1月

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    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    Web of Science

  357. Development of a highly sensitive chemical method to detect a2ョ8-linked oligo/polysialic acid residues in glycoproteins blotted on the membrane. 査読有り

    "C. Sato, S. Inoue, T. Matsuda, and K. Kitajima"

    Anal. Biochem.   261 巻   頁: 191-197   1998年1月

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    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  358. Identification of oligo-N-glycolylneuraminic acid residues in mammal-derived glycoproteins by a newly developed immunochemical reagent and biochemical methods. 査読有り

    "C. Sato, K. Kitajima, S. Inoue, and Y. Inoue"

    J. Biol. Chem.   273 巻   頁: 2575-2582   1998年1月

     詳細を見る

    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  359. Development of a highly sensitive chemical method to detect a2ョ8-linked oligo/polysialic acid residues in glycoproteins blotted on the membrane. 査読有り

    C. Sato, S. Inoue, T. Matsuda, K. Kitajima

    Anal. Biochem.   261 巻   頁: 191-197   1998年1月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  360. Identification of oligo-N-glycolylneuraminic acid residues in mammal-derived glycoproteins by a newly developed immunochemical reagent and biochemical methods. 査読有り

    C. Sato, K. Kitajima, S. Inoue, Y. Inoue

    J. Biol. Chem.   273 巻   頁: 2575-2582   1998年1月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

    0021-9258

  361. Occurrence of terminal alpha 2-&gt;8-linked disialylated poly-N-acetyllactosamine chains with Le(X) and I antigenic glycotopes in tetraantennary arms of an N-linked glycoprotein isolated from rainbow trout ovarian fluid 査読有り

    Y Funakoshi, T Taguchi, C Sato, K Kitajima, S Inoue, HR Morris, A Dell, Y Inoue

    GLYCOBIOLOGY   7 巻 ( 2 ) 頁: 195 - 205   1997年3月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)   出版者・発行元:OXFORD UNIV PRESS  

    The Pronase digestion of a 54K glycoprotein present in ovarian fluid of rainbow trout yielded a major glycopeptide, Carbohydrate compositional analysis revealed that this glycopeptide was likely to possess a single large N-glycan chain having low molecular weight oligomers of N-acetylneuraminic acid (oligoNeu5Ac), Structural studies of this glycopeptide revealed novel alpha 2 --&gt; 8-linked disialylated poly-N-acetyllactosamine chains with Le(X) and I antigenic determinants on the N-linked tetraantennary core glycan, In our recent studies (Kitazume,S., Kitajima,K., Inoue,S., Inoue,Y. and Troy,F.A. (1994) J., Biol, Chem, 269, 10330-10340) we presented evidence that synthesis of alpha 2 --&gt; 8-linked polysialic acid (polySia) chains is a two-step process in which chain initiation is catalyzed by an alpha 2 --&gt; 8-sialyltransferase (alpha 2 --&gt; 8-ST; initiase) that catalyzes synthesis of the first Sia alpha 2 --&gt; 8-linkage, forming the disialic acid (diSia) unit, Sia alpha 2 --&gt; 8-Sia alpha 2 --&gt; 6-Gal-.Chain polymerization is then postulated to be catalyzed by a second enzyme, an alpha 2 --&gt; 8-polyST (''polymerase'') that converts the diSia units to polySia chains, The present structural studies leading to the discovery of alpha 2 --&gt; 8-linked disialylated units that terminate poly-N-acetyllactosamine chains in an N-linked glycoprotein is further evidence in support of our hypothesis that more than one sialyltransferase activity is required for polySia chain synthesis and polymerization.

    Web of Science

  362. Occurrence of terminal alpha2,8-linked disialylated poly-N-acetyllactosamine chains with LeX and I antigenic glycotopes in tetraantennary arms of an N-linked glycoprotein isolated from rainbow trout ovarian fluid. 査読有り

    "Y. Funakoshi, T. Taguchi, C. Sato, K. Kitajima, S. Inoue, H. R. Morris, A. Dell, and Y. Inoue"

    Glycobiology   7 巻   頁: 195-205   1997年1月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  363. Characterization of the antigenic specificity of four different anti-(alpha2,8-linked polysialic acid) antibodies using lipid-conjugated oligo/polysialic acids. 査読有り

    "C. Sato, K. Kitajima, S. Inoue, T. Seki, F. A. Troy, II, and Y. Inoue"

    J. Biol. Chem.   270 巻   頁: 18923-18928   1995年1月

     詳細を見る

    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  364. Characterization of the antigenic specificity of four different anti-(alpha2,8-linked polysialic acid) antibodies using lipid-conjugated oligo/polysialic acids. 査読有り

    C. Sato, K. Kitajima, S. Inoue, T. Seki, F. A. Troy, II, Y. Inoue

    J. Biol. Chem.   270 巻   頁: 18923-18928   1995年1月

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

  365. Structural diversity in a2,8-linked polysialic acid chains in salmonid fish egg glycoproteins. 査読有り

    C. Sato, K. Kitajima, I. Tazawa, Y. Inoue, S. Inoue, and F. A. Troy, II

    J. Biol. Chem.   268 巻   頁: 23675-23684   1993年

     詳細を見る

    担当区分:筆頭著者   記述言語:英語   掲載種別:研究論文(学術雑誌)  

  366. Structural diversity in a2,8-linked polysialic acid chains in salmonid fish egg glycoproteins. 査読有り

    C. Sato, K. Kitajima, I. Tazawa, Y. Inoue, S. Inoue, F. A. Troy, II

    J. Biol. Chem.   268 巻   頁: 23675-23684   1993年

     詳細を見る

    記述言語:英語   掲載種別:研究論文(学術雑誌)  

▼全件表示

書籍等出版物 43

  1. Role of Polysialic Acid in Schizophrenia

    Sato C., Hane M., Kitajima K.

    Comprehensive Glycoscience: Second Edition  2021年6月  ( ISBN:9780128222447

     詳細を見る

    記述言語:日本語

    DOI: 10.1016/B978-0-12-819475-1.00026-2

    Scopus

  2. Polysialic acid as an integrative decoder in nervous and reproductive systems

    Sato C., Kitajima K.

    Glycome: The Hidden Code in Biology  2021年4月  ( ISBN:9781536194371

     詳細を見る

    記述言語:日本語

    In gametes, embryos, and neural cells, huge glycans with >10 kDa are often attached on glycoconjugates. Of those, the polysialic acid (polySia) modifies the neural cell adhesion molecules and other particular proteins, playing multiple roles in regulation of cell surface phenomena. Underlying mechanisms for the polySia-related functions are twofold. One is due to structural diversity of polySia arisen from differences in the Sia species, the inter-residue linkage, and the degree of polymerization (DP). Significance of the DP has been clarified, and not only lectins but also physiologically active molecules recognize the polymerized structures of Sia in a DP-dependent manner to trigger the different downstream signals. The other is based on the repulsive and attractive interactions of polySia with polySia itself and other binding counterpart molecules including BDNF and FGF2. Here we show that, as a code for cell surface event, the polymerized structures of Sia are expressed and interacted with various decoders, such as Siglecs, BDNF, FGF2, and dopamine, which specifically bind each of their diverse structures, diSia, triSia, oligoSia and polySia. Especially, polySia is shown to display repulsive and attractive fields at the same time to implement integrated functions of various related physiologically active molecules.

    Scopus

  3. 糖鎖生物学 : 生命現象と糖鎖情報

    北島 健, 佐藤 ちひろ, 門松 健治, 加藤 晃一 ( 担当: 共著)

    名古屋大学出版会  2020年  ( ISBN:9784815809812

     詳細を見る

    記述言語:日本語 著書種別:学術書

    CiNii Books

  4. ST8 alpha-N-acetyl-neuraminide alpha- 2,8-sialyltransferase 2 (ST8SIA2)

    Sato C.

    Handbook of Glycosyltransferases and Related Genes, Second Edition  2014年1月  ( ISBN:9784431542391

     詳細を見る

    記述言語:日本語

    ST8 α-N-acetyl-neuraminide α-2,8-sialyltransferase 2 (ST8SIA2) is a member of a family of α2,8-sialyltransferases that transfer sialic acid from CMP-sialic acid onto sialic acid residues of other sialoglycans to generate α2,8-linked sialoglycans. ST8SIA2 is characterized by the ability to synthesize polysialic acid (polySia) structure and can therefore be subclassified as a polysialyltransferase. Both ST8SIA2 and the related polysialyltransferase ST8SIA4 (refer to the Chap. ST8SIA4) are capable of synthesizing extraordinary long polySia chains with degrees of polymerization (DP) of up to 400. ST8SIA2 is a type II transmembrane protein, similar to many other glycosyltransferases, and is composed of 375 amino acids with six N-glycans. This enzyme contains sialyl-motif (SM) L, S, VS, and III domains.

    DOI: 10.1007/978-4-431-54240-7_77

    Scopus

  5. Polysialic acid

    Sato C.

    Sialobiology: Structure, Biosynthesis and Function. Sialic Acid Glycoconjugates in Health and Disease  2013年8月  ( ISBN:9781608050673

     詳細を見る

    記述言語:日本語

    Sialic acids (Sia) are involved in many biological activities and are commonly present as monosialyl residues at the non-reducing terminal end of glycoconjugates. Occasionally, polymerized structures in the form of disialic acid (diSia), oligosialic acid (oligoSia), and polysialic acid (polySia) appear in glycoconjugates. In particular, polySia is known to be a common epitope from bacteria to humans and is one of the most famous, biologically-important glycotopes in vertebrates. The biological functions of polySia, especially on neural cell adhesion molecules (NCAMs), have been well studied and an indepth body of knowledge concerning polySia has been accumulated. However, considerably less attention has been paid to glycoproteins containing di- and oligoSia groups. As the analytical methods used to detect oligo/polymerized structures have been improved, glycoproteins containing di/oligo/polySia chains have been identified with an increasing frequency in nature. In addition, more sophisticated genetic techniques have helped elucidate the underlying mechanisms of polySia-mediated activities. In this chapter, the recent advances in the study of di-, oligo- and polySia residues on glycoproteins, including their distribution, chemical properties, biosynthetic pathways, and functions are described. © 2013 Bentham Science Publishers. All rights reserved.

    DOI: 10.2174/9781608053865113010005

    Scopus

  6. Advanced Technologies in Sialic Acid and Sialoglycoconjugate Analysis in Top Curr Chem

    Kitajima K, Varki N, Sato C.( 担当: 共著)

    Springer  2015年 

     詳細を見る

    記述言語:英語

  7. Advanced Technologies in Sialic Acid and Sialoglycoconjugate Analysis in Top Curr Chem

    Kitajima K, Varki N, Sato C( 担当: 共著)

    Springer  2015年 

     詳細を見る

    担当ページ:75-103   記述言語:英語

  8. Frontal Affinity Chromatography in the Methods in Molecular Biology

    Sato, C. ( 担当: 単著)

    Springer  2014年 

     詳細を見る

    記述言語:英語

  9. Flagellasialin in the Glycoscience: Biology and Medicine

    Kanazawa, T., Suzuki, E., Miyata, S., Sato, C. and Kitajima, K. ( 担当: 共著)

    Springer  2014年 

     詳細を見る

    記述言語:英語

  10. Polysialyltransferase assay in the Glycoscience: Biology and Medicine

    Hane, M., Kitajima, K. and Sato, C. ( 担当: 共著)

    Springer  2014年 

     詳細を見る

    記述言語:英語

  11. Polysialic acid in the Glycoscience: Biology and Medicine

    Sato, C. and Kitajima, K. ( 担当: 共著)

    Springer,  2014年 

     詳細を見る

    記述言語:英語

  12. ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 (ST8SIA2)in Handbook of Glycosyltransferases and related genes

    Sato C( 担当: 単著)

    Springer  2014年 

     詳細を見る

    記述言語:英語

  13. ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2 (ST8SIA2)in Handbook of Glycosyltransferases and related genes

    Sato C( 担当: 単著)

    Springer  2014年 

     詳細を見る

    担当ページ:781-795   記述言語:英語

  14. Flagellasialin in the Glycoscience: Biology and Medicine

    Kanazawa, T, Suzuki, E, Miyata, S, Sato, C, Kitajima, K( 担当: 共著)

    Springer  2014年 

     詳細を見る

    担当ページ:1-6   記述言語:英語

  15. Polysialyltransferase assay in the Glycoscience: Biology and Medicine

    Hane, M, Kitajima, K, Sato, C( 担当: 共著)

    Springer  2014年 

     詳細を見る

    担当ページ:1-5   記述言語:英語

  16. Polysialic acid in the Glycoscience: Biology and Medicine

    Sato, C, Kitajima, K( 担当: 共著)

    Springer,  2014年 

     詳細を見る

    担当ページ:1-7   記述言語:英語

  17. Frontal Affinity Chromatography in the Methods in Molecular Biology

    Sato, C( 担当: 単著)

    Springer  2014年 

     詳細を見る

    担当ページ:257-264   記述言語:英語

  18. Sialobiology: Structure, Function and Biosynthesis

    Sato C( 担当: 共著)

    Bentham Science  2013年 

     詳細を見る

    記述言語:英語

  19. Sialobiology: Structure, Function and Biosynthesis

    Sato C( 担当: 共著)

    Bentham Science  2013年 

     詳細を見る

    担当ページ:33-75   記述言語:英語

  20. Methods in Enzymology・ Analysis of glycan-protein interaction by frontal affinity chromatography and Biacore.

    Sato, C., Yamakawa, N., and Kitajima, K.( 担当: 共著)

    Elsevir science  2010年 

     詳細を見る

    記述言語:英語

  21. Methods in Enzymology・ Analysis of glycan-protein interaction by frontal affinity chromatography and Biacore.

    Sato, C, Yamakawa, N, Kitajima, K( 担当: 共著)

    Elsevir science  2010年 

     詳細を見る

    担当ページ:219-232   記述言語:英語

  22. Carbohydrate Recognition: Biological problems, methods, and applications

    Ken Kitajima and Chihiro Sato (Editors: Binghe Wang, Geer-Jan Boons)( 担当: 共著)

    John Wiley and Sons  2009年 

     詳細を見る

    記述言語:英語

  23. Carbohydrate Recognition: Biological problems, methods, and applications

    Ken Kitajima, Chihiro Sato, Binghe Wang, Geer-Jan Boons( 担当: 共著)

    John Wiley and Sons  2009年 

     詳細を見る

    担当ページ:in press   記述言語:英語

  24. Membrane microdomain as a platform of carbohydrate-mediated interactions during early development of medaka fish.

    Adachi, T., Sato, C., and Kitajima, K.( 担当: 共著)

    KINPO-DO  2008年 

     詳細を見る

    記述言語:英語

  25. Glycoscience Lab Manual・Structure analysis of oligo/polysialic acid

    C. Sato and K. Kitajima( 担当: 共著)

    KINPO-DO  2008年 

     詳細を見る

    記述言語:英語

  26. Glycoscience Lab Manual・Labeling of oligosialic acid

    C. Sato( 担当: 共著)

    KINPO-DO  2008年 

     詳細を見る

    記述言語:英語

  27. Glycoscience Lab Manual・Labeling of oligosialic acid

    C. Sato( 担当: 共著)

    KINPO-DO  2008年 

     詳細を見る

    担当ページ:24-27   記述言語:英語

  28. Membrane microdomain as a platform of carbohydrate-mediated interactions during early development of medaka fish.

    Adachi, T, Sato, C, Kitajima, K( 担当: 共著)

    KINPO-DO  2008年 

     詳細を見る

    担当ページ:299-302   記述言語:英語

  29. Glycoscience Lab Manual・Structure analysis of oligo/polysialic acid

    C. Sato, K. Kitajima( 担当: 共著)

    KINPO-DO  2008年 

     詳細を見る

    担当ページ:77-81   記述言語:英語

  30. 遺伝子医学MOOK 糖鎖と病気・ポリシアル酸

    佐藤ちひろ、北島 健( 担当: 共著)

    メディカルデュー  2005年 

     詳細を見る

    記述言語:日本語

  31. 未来を拓く糖鎖科学・オリゴシアル酸の標識

    ( 担当: 共著)

    金芳堂  2005年 

     詳細を見る

    記述言語:日本語

    オリゴシアル酸の標識

  32. 未来を拓く糖鎖科学・オリゴシアル酸の標識

    ( 担当: 共著)

    金芳堂  2005年 

     詳細を見る

    担当ページ:12-13   記述言語:日本語

    オリゴシアル酸の標識

  33. 遺伝子医学MOOK 糖鎖と病気・ポリシアル酸

    佐藤ちひろ, 北島 健( 担当: 共著)

    メディカルデュー  2005年 

     詳細を見る

    担当ページ:186-191   記述言語:日本語

  34. Recent Research Developments in Analytical Biochemistry・Detection of di/oligo/polysialic acid units in glycoproteins

    "C. Sato, and K. Kitajima"( 担当: 共著)

    Transworld research network  2002年 

     詳細を見る

    記述言語:英語

  35. Recent Research Developments in Analytical Biochemistry・Detection of di/oligo/polysialic acid units in glycoproteins

    C. Sato, K. Kitajima( 担当: 共著)

    Transworld research network  2002年 

     詳細を見る

    担当ページ:201-215   記述言語:英語

  36. Leukocyte typing VII・Carbohydrate-recognizing monoclonal antibodies as revealed by ELISA using phosphatidylethanolamine-conjugated oligosaccharides as antigens

    C. Sato and K. Kitajima( 担当: 共著)

    OXFORD  2001年 

     詳細を見る

    記述言語:英語

  37. Leukocyte typing VII・Oligosialic acid as a differentiation-associated antigen in human haematopoietic cell line HL60.

    C. Sato and K. Kitajima( 担当: 共著)

    OXFORD  2001年 

     詳細を見る

    記述言語:英語

  38. Leukocyte typing VII・Carbohydrate-recognizing monoclonal antibodies as revealed by ELISA using phosphatidylethanolamine-conjugated oligosaccharides as antigens

    C. Sato, K. Kitajima( 担当: 共著)

    OXFORD  2001年 

     詳細を見る

    担当ページ:168-169   記述言語:英語

  39. Leukocyte typing VII・Oligosialic acid as a differentiation-associated antigen in human haematopoietic cell line HL60.

    C. Sato, K. Kitajima( 担当: 共著)

    OXFORD  2001年 

     詳細を見る

    担当ページ:208-211   記述言語:英語

  40. Sialobiology and Other Novel Form of Glycosylation・Occurrence of a2,8-linked oligosialic acid residues in mammalian glycoproteins.

    K. Kitajima, C. Sato, N. Honda, T. Matsuda, M.-H. Yokoyama, B. E. Close, and K. J. Colley( 担当: 共著)

    Gakushin  1999年 

     詳細を見る

    記述言語:英語

  41. Sialobiology and Other Novel Form of Glycosylation・Occurrence of a2,8-linked oligosialic acid residues in mammalian glycoproteins.

    K. Kitajima, C. Sato, N. Honda, T. Matsuda, M.-H. Yokoyama, B. E. Close, K. J. Colley( 担当: 共著)

    Gakushin  1999年 

     詳細を見る

    担当ページ:69-76   記述言語:英語

  42. KDN(=デアミノノイラミン酸)-転移酸素およびポリKDN-転移酵素の研究 : 各種KDN-転移酵素の利用による機能性KDN-複合糖質の造成と活用

    井上 康男( 担当: 単著)

    井上康男  1994年 

     詳細を見る

    記述言語:日本語

    CiNii Books

  43. KDN(=デアミノノイラミン酸)-転移酸素およびポリKDN-転移酵素の研究 : 各種KDN-転移酵素の利用による機能性KDN-複合糖質の造成と活用

    井上 康男( 担当: 単著)

    井上康男  1994年 

     詳細を見る

    担当ページ:.   記述言語:日本語

▼全件表示

MISC 24

  1. 胎仔期マウス大脳皮質形成におけるヒアルロン酸の発現変動と細胞外基質としての機能

    武智美奈, 大島健司, 灘野大太, 松田幹, 佐藤ちひろ, 北島健, 北川裕之, 宮田真路, 宮田真路  

    日本生化学会大会(Web)92nd 巻   2019年

     詳細を見る

  2. Hsp70の酸性複合糖質結合活性の発見 : 糖の意外な働き

    原田 陽一郎, 佐藤 ちひろ, 北島 健  

    化学と生物 : 日本農芸化学会会誌 : 生命・食・環境55 巻 ( 1 ) 頁: 22 - 26   2017年1月

     詳細を見る

    記述言語:日本語   出版者・発行元:日本農芸化学会 ; 1962-  

    CiNii Books

  3. The Out of Africa and mental disorders: Adaptation with reduction in STX promoter activity

    Naoko Fujito, Yoko Satta, Masaya Hane, Atsushi Matsui, Kenta Yashima, Ken Kitajima, Chihiro Sato, Naoyuki Takahata, Toshiyuki Hayakawa  

    GENES & GENETIC SYSTEMS91 巻 ( 6 ) 頁: 343 - 343   2016年12月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:GENETICS SOC JAPAN  

    Web of Science

  4. A Uniquely Human Evolutionary Change in ST8Sia-II Impacts Enzyme Stability and Polysialic Acid Function

    Michael Vaill, Masaya Hane, Yuko Naito-Matsui, Sandra Diaz, Leela Davies, Ken Kitajima, Chihiro Sato, Ajit Varki  

    GLYCOBIOLOGY26 巻 ( 12 ) 頁: 1423 - 1423   2016年12月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:OXFORD UNIV PRESS INC  

    Web of Science

  5. Spread of reduced activity of STX promoter throughout Great Journey

    Naoko Fujito, Yoko Satta, Masaya Hane, Atsushi Matsui, Ken Kitajima, Chihiro Sato, Toshiyuki Hayakawa  

    GENES & GENETIC SYSTEMS90 巻 ( 6 ) 頁: 379 - 379   2015年12月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:GENETICS SOC JAPAN  

    Web of Science

  6. Adaptive evolution of the promoter region of the Sialyltransferase 8B (STX) gene

    Naoko T. Fujito, Toshiyuki Hayakawa, Masaya Hane, Ken Kitajima, Chihiro Sato, Yoko Satta  

    GENES & GENETIC SYSTEMS89 巻 ( 6 ) 頁: 327 - 327   2014年12月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:GENETICS SOC JAPAN  

    Web of Science

  7. The Synthesis of Sialo-containing Glycopolymers by pi-Allyl Nickel Catalyzed Coordination Polymerization

    Shuichi Ohira, Yu Yasuda, Chihiro Sato, Ken KItajima, Ikuyoshi Tomita, Takashi Takahashi, Hiroshi Tanaka  

    GLYCOBIOLOGY24 巻 ( 11 ) 頁: 1119 - 1120   2014年11月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:OXFORD UNIV PRESS INC  

    Web of Science

  8. An anti-schizophrenic drug affects the surface expression of polySia-NCAM in IMR-32 human neuroblastoma cells

    Saki Nishimura, Masaya Hane, Yuki Niimi, Ken Kitajima, Chihiro Sato  

    GLYCOBIOLOGY24 巻 ( 11 ) 頁: 1193 - 1193   2014年11月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:OXFORD UNIV PRESS INC  

    Web of Science

  9. Insight into single nucleotide polymorphisms (SNPs) of the polysialyltransferase ST8SIA2/STX in psychiatric disorders

    Masaya Hane, Saki Nishimura, Toshiyuki Hayakawa, Ken Kitajima, Chihiro Sato  

    GLYCOBIOLOGY24 巻 ( 11 ) 頁: 1206 - 1206   2014年11月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:OXFORD UNIV PRESS INC  

    Web of Science

  10. Functional analysis of tissue-specific post-translational modification of springtime hormone TSH

    IKEGAMI Keisuke, LIAO Xiao‐Hui, HOSHINO Yuta, ONO Hiroko, OTA Wataru, ITO Yuka, NISHIWAKI‐OHKAWA Taeko, SATO Chihiro, KITAJIMA Ken, IIGO Masayuki, SHIGEYOSHI Yasufumi, YAMADA Masanobu, MURATA Yoshiharu, REFETOFF Samuel, YOSHIMURA Takashi  

    時間生物学20 巻 ( 2 ) 頁: 114   2014年10月

     詳細を見る

    記述言語:英語  

    J-GLOBAL

  11. ポリシアル酸転移酵素STX/ST8SIA2とPST/ST8SIA4のポリシアル酸生合成能の解析

    新美百希, 羽根正弥, 西村紗希, 宮田真路, 北島健, 佐藤ちひろ  

    日本糖質学会年会要旨集33rd 巻   頁: 144   2014年7月

     詳細を見る

    記述言語:日本語  

    J-GLOBAL

  12. 癌や精神疾患に関わるポリシアル酸構造に特異的な一本鎖抗体の作製と特異性評価

    羽根正弥, 羽根正弥, 羽根正弥, 長江雅倫, 池田明美, 山口芳樹, 北島健, 北島健, 北島健, 佐藤ちひろ, 佐藤ちひろ, 佐藤ちひろ  

    日本農芸化学会大会講演要旨集(Web)2014 巻   2014年

     詳細を見る

  13. Polysialic acid on flagellasialin is involved in sperm motility

    Shinji Miyata, Chihiro Sato, Hironobu Kumita, Masaru Toriyama, Ken Kitajima  

    ZOOLOGICAL SCIENCE23 巻 ( 12 ) 頁: 1171 - 1171   2006年12月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:ZOOLOGICAL SOC JAPAN  

    Web of Science

  14. An N-terminal 130 kDa fragment of a fourth sea urchin sperm receptor for egg jelly module protein, REJ4, is secreted during acrosome reaction

    Shinji Miyata, Chihiro Sato, Masaru Toriyama, Ken Kitajama  

    ZOOLOGICAL SCIENCE22 巻 ( 12 ) 頁: 1456 - 1456   2005年12月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:ZOOLOGICAL SOC JAPAN  

    Web of Science

  15. Capacitation-induced changes of the surface distribution of sialoglycotopes on pig sperm

    Lian Xue, Shinji Miyata, Chihiro Sato, Ken Kitajima  

    ZOOLOGICAL SCIENCE22 巻 ( 12 ) 頁: 1456 - 1456   2005年12月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:ZOOLOGICAL SOC JAPAN  

    Web of Science

  16. ブタ精子表面に新しく見出されたシアロ糖鎖エビトープの解析

    せつ蓮, 宮田真路, 佐藤ちひろ, 北島健  

    生化学77 巻 ( 6 ) 頁: 571   2005年6月

     詳細を見る

    記述言語:日本語  

    J-GLOBAL

  17. The 130 kDa glycoprotein is secreted from sperm during acrosome reaction of sea urchin, Hemicentrotus pulcherrimus

    Shinji Miyata, Chihiro Sato, Masaru Toriyama, Noritaka Hirohashi, Victor Vacquier, Ken Kitajima  

    ZOOLOGICAL SCIENCE21 巻 ( 12 ) 頁: 1292 - 1292   2004年12月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:ZOOLOGICAL SOC JAPAN  

    Web of Science

  18. A major ganglioside from Hemicentrotus pulcherrimus sperm specifically interacts with phospholipids

    Nao Yamakawa, Chihiro Sato, Ken Kitajima  

    ZOOLOGICAL SCIENCE21 巻 ( 12 ) 頁: 1292 - 1292   2004年12月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:ZOOLOGICAL SOC JAPAN  

    Web of Science

  19. Development of sensitive chemical and immunochemical methods for detecting sulfated sialic acids and their application to localization and quantitation studies of sea urchin sperm and eggs

    N Yamakawa, E Maehashi, S Miyata, C Sato, K Furuhata, K Kitajima  

    GLYCOBIOLOGY14 巻 ( 11 ) 頁: 1146 - 1146   2004年11月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:OXFORD UNIV PRESS INC  

    Web of Science

  20. Occurrence and characterization of a novel sulfated alpha 2,9-linked polysialic acid-containing glycoprotein in sea urchin sperm flagellum

    S Miyata, C Sato, K Kitajima  

    GLYCOBIOLOGY14 巻 ( 11 ) 頁: 1146 - 1146   2004年11月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:OXFORD UNIV PRESS INC  

    Web of Science

  21. Mouse T cell CD166 is a disialic acid-containing glycoprotein and involved in T cell activation

    C Sato, K Nohara, T Matsuda, K Kitajima  

    GLYCOBIOLOGY14 巻 ( 11 ) 頁: 1136 - 1136   2004年11月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:OXFORD UNIV PRESS INC  

    Web of Science

  22. Mouse heat shock protein 70 recognizes negatively charged glycolipids and phospholipids

    Y Harada, C Sato, K Kitajima  

    GLYCOBIOLOGY14 巻 ( 11 ) 頁: 1101 - 1102   2004年11月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:OXFORD UNIV PRESS INC  

    Web of Science

  23. Effects of exogenously administered mannose and deaminoneuraminic acid (KDN) to mice or murine cultured cells on the metabolism of KDN

    S Go, C Sato, K Kitajima  

    GLYCOBIOLOGY14 巻 ( 11 ) 頁: 1166 - 1167   2004年11月

     詳細を見る

    記述言語:英語   掲載種別:研究発表ペーパー・要旨(国際会議)   出版者・発行元:OXFORD UNIV PRESS INC  

    Web of Science

  24. ウニ受精におけるシアル酸を介する相互作用と脂質ラフトの重要性

    前橋絵梨, 宮田真路, 松本晴美, 松田幹, 佐藤ちひろ, 北島健  

    生化学74 巻 ( 8 ) 頁: 777   2002年8月

     詳細を見る

    記述言語:日本語  

    J-GLOBAL

▼全件表示

講演・口頭発表等 168

  1. 遺伝的及び環境要因による糖鎖発現制御から脳の健康を考える 招待有り

    佐藤ちひろ

    第11回グライコバイオロジクス研究会   2021年1月21日  第11回グライコバイオロジクス研究会

     詳細を見る

    開催年月日: 2021年1月

    記述言語:日本語   会議種別:口頭発表(基調)  

    開催地:名古屋   国名:日本国  

  2. オリゴシアル酸転移酵素ST8Sia6の発現はメラノーマを悪性化する

    畑中理菜、荒木映莉乃、羽根正弥、Wu Di、北島健、佐藤ちひろ

    第93回日本生化学会大会  2020年9月14日  日本生化学会

     詳細を見る

    開催年月日: 2020年9月

    記述言語:英語   会議種別:口頭発表(一般)  

    開催地:Web   国名:日本国  

  3. 環境要因としてのシアル酸投与と脳領域特異的ポリシアル酸発現の解析

    高橋佑佳、阿部智佳羅、羽根正弥、呉迪、北島 健、佐藤ちひろ

    第84回日本生化学会中部支部例会  2020年9月14日  日本生化学会中部支部

     詳細を見る

    開催年月日: 2020年9月

    記述言語:日本語   会議種別:ポスター発表  

    開催地:Web   国名:日本国  

  4. 各種脊椎動物ポリシアル酸転移酵素ST8Sia2がもたらす種特異的なpolySia-NCAM構造の解析

    村井良、羽根正弥、呉迪、北島健、佐藤ちひろ

    第93回日本生化学会大会  2020年9月14日  日本生化学会

     詳細を見る

    開催年月日: 2020年9月

    記述言語:日本語   会議種別:ポスター発表  

    開催地:Web   国名:日本国  

  5. ラクタム化シアル酸誘導体の合成とその分解反応に関する研究.

    大野ひろみ、安藤弘宗、川上信彦、岩田章子、佐藤ちひろ、北島健、石田秀治、木曽真

    日本農芸化学会2009年度大会 

     詳細を見る

    開催年月日: 2009年3月

    記述言語:日本語   会議種別:ポスター発表  

    国名:日本国  

  6. 魚類CMP-シアル酸合成酵素の構造と性質

    藤田明子、安川裕子、佐藤ちひろ、北島健

    日本農芸化学会2009年度大会 

     詳細を見る

    開催年月日: 2009年3月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  7. ポリシアル酸と脳由来神経栄養因子の相互作用の解析

    金戸幸弘、北島健、佐藤ちひろ

    日本農芸化学会2009年度大会 

     詳細を見る

    開催年月日: 2009年3月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  8. ポリシアル酸とFGF-2の相互作用の解析.

    小野明日香、金戸幸弘、北島 健、佐藤ちひろ

    日本農芸化学会2009年度大会 

     詳細を見る

    開催年月日: 2009年3月

    記述言語:日本語   会議種別:ポスター発表  

    国名:日本国  

  9. Polysialic acid is not a negative regulator any longer in neurogenesis and neuronal functions: A new finding of its binding to a particular group of neurotransmitters. 国際会議

    Ken Kitajima, Ryo Isomura, and Chihiro Sato

    Gordon Research Conference on Glycobiology,  

     詳細を見る

    開催年月日: 2009年1月

    記述言語:英語   会議種別:ポスター発表  

    国名:アメリカ合衆国  

  10. 昆虫細胞由来シアル酸9-リン酸合成酵素の構造と基質特異性の解析

    濱口香代、郷慎司、佐藤ちひろ、小林迪弘、池田素子、北島健

    第81回日本生化学会大会 

     詳細を見る

    開催年月日: 2008年12月

    記述言語:日本語   会議種別:ポスター発表  

    国名:日本国  

  11. 哺乳類シアロ糖タンパク質のデアミノノイラミン酸 (KDN) 修飾糖タンパク質への改変.

    中島優子、藤田明子、佐藤ちひろ、北島健

    第81回日本生化学会大会 

     詳細を見る

    開催年月日: 2008年12月

    記述言語:日本語   会議種別:ポスター発表  

    国名:日本国  

  12. 酸性多糖と神経栄養因子との相互作用解析. 国際会議

    金戸幸弘、北島健、佐藤ちひろ

    第81回日本生化学会大会 

     詳細を見る

    開催年月日: 2008年12月

    記述言語:英語   会議種別:口頭発表(一般)  

    国名:日本国  

  13. 抗ジシアル酸抗体が認識する急性期タンパク質の同定. 国際会議

    安川然太、北島健、佐藤ちひろ

    第81回日本生化学会大会 

     詳細を見る

    開催年月日: 2008年12月

    記述言語:英語   会議種別:ポスター発表  

    国名:日本国  

  14. 化学的検出法を用いた天然におけるサイクリックシアル酸の局在検索.

    岩田章子、佐藤ちひろ、安藤弘宗、石田秀治、木曽真、神奈木玲児、北島健

    第81回日本生化学会大会 

     詳細を見る

    開催年月日: 2008年12月

    記述言語:日本語   会議種別:ポスター発表  

    国名:日本国  

  15. ポリシアル酸は特定の神経伝達物質と相互作用する. 国際会議

    磯村遼、北島健、佐藤ちひろ

    第81回日本生化学会大会 

     詳細を見る

    開催年月日: 2008年12月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  16. mAb.A2B5の抗原特異性の決定とマウス脳発達段階におけるmAb.A2B5反応性オリゴシアル酸含有糖タンパク質の発現解析 国際会議

    猪子恵未、西浦祐二、田中浩士、高橋孝志、北島健、佐藤ちひろ

    第81回日本生化学会大会 

     詳細を見る

    開催年月日: 2008年12月

    記述言語:英語   会議種別:ポスター発表  

    国名:日本国  

  17. ポリシアル酸の新機能

    佐藤ちひろ

    第6回日本糖鎖科学コンソーシアムシンポジウム-糖鎖研究と他領域との統合- 

     詳細を見る

    開催年月日: 2008年12月

    記述言語:日本語   会議種別:シンポジウム・ワークショップ パネル(指名)  

    国名:日本国  

  18. ウニ配偶子生体膜マイクロドメイン間接着に関わるガングリオシド-中性糖脂質相互作用の発見.

    山川奈緒、佐藤ちひろ、北島健

    第81回日本生化学会大会 

     詳細を見る

    開催年月日: 2008年12月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  19. Novel insights into the novel binding sites of the sialic acid biding Ig-like lectin-7 (Siglec-7) gained by in silico docking studies. 国際会議

    A one-day symposium on Sialyltransferases, Functional Glycomics, and Genomics of Zebrafish, 

     詳細を見る

    開催年月日: 2008年11月

    記述言語:英語   会議種別:シンポジウム・ワークショップ パネル(指名)  

    国名:台湾  

  20. Membrane microdomains from early gastrula embryos of medaka are a platform of E-cadherin- and LeX-mediated cell-cell interactions during epiboly. 14th

    Japanese Medaka and Zebrafish Meeting 

     詳細を見る

    開催年月日: 2008年9月

    記述言語:英語   会議種別:口頭発表(一般)  

    国名:日本国  

  21. CMP-[14C]デアミノノイラミン酸(KDN)のワンポット酵素合成法の確立

    中島優子、藤田明子、佐藤ちひろ、北島健

    糖鎖科学名古屋拠点「若手の力」フォーラム第6回 

     詳細を見る

    開催年月日: 2008年9月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  22. 酸性多糖と神経栄養因子との相互作用解析

    金戸幸広、北島 健、佐藤ちひろ

    糖鎖科学名古屋拠点「若手の力」フォーラム第6回 

     詳細を見る

    開催年月日: 2008年9月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  23. 鱗翅目昆虫細胞におけるシアル酸9-リン酸合成酵素ホモログの同定.

    濱口香代、郷慎司、佐藤ちひろ、小林迪弘、池田素子、北島健

    糖鎖科学名古屋拠点「若手の力」フォーラム第6回 

     詳細を見る

    開催年月日: 2008年8月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  24. ポリシアル酸の神経伝達分子結合活性の発見と性質

    磯村遼、北島健、佐藤ちひろ

    FCCAグライコサイエンス若手フォーラム2008 

     詳細を見る

    開催年月日: 2008年8月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  25. CMP-シアル酸合成酵素の基質認識および細胞内局在の分子機構の解明

    藤田明子, 佐藤ちひろ, Tiralongo, Joe, Münster-Kühnel, Anja K., Gerardy-Schahn, Rita, 北島健

    第28回日本糖質学会年会 

     詳細を見る

    開催年月日: 2008年8月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  26. 抗ガングリオシド抗体A2B5が認識する糖タンパク質のマウス新生児脳における発現.

    猪子恵未、西浦祐二、田中浩士、高橋孝志、北島健、佐藤ちひろ

    FCCAグライコサイエンス若手フォーラム2008 

     詳細を見る

    開催年月日: 2008年8月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  27. ウニ卵膜マイクロドメインに対する単クローン抗体の認識エピトープ解析.

    中村奈央子、前橋絵梨、山川奈緒、佐藤ちひろ、鳥山優、北島健

     FCCAグライコサイエンス若手フォーラム2008 

     詳細を見る

    開催年月日: 2008年8月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  28. Complex formation between polysialic acid and brain derived neurotrophic factor (BDNF). 国際会議

    Chihiro Sato, Yukihiro Kanato, and Ken Kitajima:

    24th International Carbohydrate Symposium, 

     詳細を見る

    開催年月日: 2008年7月 - 2008年8月

    記述言語:英語   会議種別:ポスター発表  

  29. In vitro and in silico docking studies of heat shock protein (Hsp) 70 with sulfatide. 国際会議

    Nao Yamakawa, Yoichiro Harada, Chihiro Sato, Gerard Vergoten, Ken Kitajima

    24th International Carbohydrate Symposium, 

     詳細を見る

    開催年月日: 2008年7月 - 2008年8月

    記述言語:英語   会議種別:ポスター発表  

  30. Brain-derived neurotrophic factor binds to polysialic acid directly depending on degree of polymerization. 国際会議

    Yukihiro Kanato, Ken Kitajima, Chihiro Sato

    SialoGlyco Conference 2008 

     詳細を見る

    開催年月日: 2008年7月

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  31. New Findings on the Expression of Non-human Sialic Acid Neu5Gc, and KDN in Cultured Human Cells. 国際会議

    SialoGlyco Conference 2008 

     詳細を見る

    開催年月日: 2008年7月

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  32. Occurrence of the Cyclic Sialic Acid in Mammalian Cells and Tissues As Demonstrated by Chemical Methods. 国際会議

    K. Kitajima, S.Iwata, N. Kawakami, C. Sato, H. Ando, H. Ohno, H. Ishida, M. Kiso, O. Taguchi, R. Kannagi:

    SialoGlyco Conference 2008 

     詳細を見る

    開催年月日: 2008年7月

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  33. One-pot Enzymatic Synthesis of CMP-[14C]deaminoneuraminic Acid (KDN). 国際会議

    Yuko Nakajima, Akiko Fujita, Chihiro Sato, and Ken Kitajima

    SialoGlyco Conference 2008 

     詳細を見る

    開催年月日: 2008年7月

    記述言語:英語   会議種別:ポスター発表  

  34. In silico binding studies predict novel sialic acid binding sites on the sialic acid binding Ig-like lectin-7 (Siglec-7) 国際会議

    Nao Yamakawa, Chihiro Sato, Paul R. Crocker, Gérard Vergoten, and Ken Kitajima: I

    SialoGlyco Conference 2008 

     詳細を見る

    開催年月日: 2008年7月

    記述言語:英語   会議種別:ポスター発表  

  35. Identification of the nuclear export signals that regulate the intracellular localization of the mouse CMP-sialic acid synthetase. 国際会議

    Akiko Fujita, Chihiro Sato, and Ken Kitajima

    SialoGlyco Conference 2008 

     詳細を見る

    開催年月日: 2008年7月

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  36. CMP-デアミノノイラミン酸(CMP-KDN)のワンポット酵素合成法の確立

    日本農芸化学会2008年度大会 

     詳細を見る

    開催年月日: 2008年3月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  37. 抗ジシアル酸が認識するマウス血清タンパク質の同定

    安川然太、北島健、佐藤ちひろ

    日本農芸化学会2008年度大会 

     詳細を見る

    開催年月日: 2008年3月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  38. 分子モデリング法による熱ショック蛋白質の酸性糖脂質結合性の解析

    山川奈緒、原田陽一郎、佐藤ちひろ、Gerard Vergoten、北島健

    日本農芸化学会2008年度大会 

     詳細を見る

    開催年月日: 2008年3月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  39. マウスCMP-シアル酸合成酵素の核外移行シグナル (NES) の同定

    藤田明子、佐藤ちひろ、北島 健

     詳細を見る

    開催年月日: 2008年3月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  40. 脊椎動物CMP-シアル酸合成酵素の基質認識および細胞内局在の分子機構の解明.

    藤田明子, 佐藤ちひろ, Tiralongo, Joe, Münster-Kühnel, Anja K., Gerardy-Schahn, Rita, 北島健

    第28回日本糖質学会年会 

     詳細を見る

    開催年月日: 2007年3月

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  41. 分子シミュレーションによる熱ショックタンパク質の酸性糖脂質結合性の解析

    山川 奈緒、原田陽一郎、佐藤ちひろ、Gerard Vergoten, 北島 健

     詳細を見る

    開催年月日: 2007年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  42. Short-term regulation of polysialic acid expression in microglia

    Gordon Research Conference on Glycobiology 

     詳細を見る

    開催年月日: 2007年

    記述言語:日本語   会議種別:口頭発表(招待・特別)  

  43. A rapid clearance of polysialic acid on microglia by inflammatory stimulation 国際会議

    3rd International Meeting on polysialic acid 

     詳細を見る

    開催年月日: 2007年

    記述言語:英語   会議種別:ポスター発表  

  44. シアル酸重合体の生物学的意義の解明

    佐藤ちひろ、矢部宇一郎、安川然太1,2、宮田真路、澤田 誠、北島 健

    文科省特定領域研究 糖鎖によるタンパク質と分子複合体の機能調節 第5回公開シンポジウム 

     詳細を見る

    開催年月日: 2007年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  45. ジシアリル化修飾をうけた血清糖タンパク質の同定

    安川然太、佐野琴音、小川温子、北島 健、佐藤ちひろ

    日本農芸化学会2007年度大会 

     詳細を見る

    開催年月日: 2007年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  46. 脊椎動物由来CMP-シアル酸合成酵素によるデアミノノイラミン酸(KDN)の認識機構

    藤田 明子、佐藤ちひろ、北島 健

    日本農芸化学会2007年度大会 

     詳細を見る

    開催年月日: 2007年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  47. サイクリックシアル酸グリコシドの化学的性質の解析

    岩田章子、川上信彦、佐藤ちひろ、安藤弘宗、木曽 真、神奈木玲児、北島 健

    日本農芸化学会2007年度大会 

     詳細を見る

    開催年月日: 2007年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  48. 酸性糖脂質による70kDa熱ショックタンパク質の複合体形成

    原田陽一郎、佐藤ちひろ、北島 健

    日本農芸化学会2007年度大会 

     詳細を見る

    開催年月日: 2007年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  49. 70kDa-熱ショックタンパク質の酸性糖脂質誘導性の高分子複合体形成能の発見

    原田陽一郎、佐藤ちひろ、北島 健

    第27回 日本糖質学会年会 

     詳細を見る

    開催年月日: 2007年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  50. サイクリックシアル酸グリコシドの酸加水分解産物の同定

    川上信彦、岩田章子、佐藤ちひろ、安藤弘宗、木曽 真、神奈木玲児、北島健

    糖鎖科学名古屋拠点 若手の力フォーラム 第5回 

     詳細を見る

    開催年月日: 2007年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  51. O-型糖鎖上のポリシアル酸の生合成機構の解明

    朝比奈慎二、佐藤ちひろ、松野みどり、松田 幹、Karen, J. Colley, 北島 健

    糖鎖科学名古屋拠点 若手の力フォーラム 第4回 

     詳細を見る

    開催年月日: 2006年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  52. ポリシアル酸の探求と活用

    佐藤ちひろ

    第5回 糖鎖分科会 

     詳細を見る

    開催年月日: 2006年

    記述言語:日本語   会議種別:口頭発表(招待・特別)  

    国名:日本国  

  53. ミクログリア細胞におけるポリシアル酸構造の発現.

    佐藤ちひろ

    文科省特定領域研究 糖鎖によるタンパク質と分子複合体の機能調節 第四回公開シンポジウム 

     詳細を見る

    開催年月日: 2006年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  54. Hsp70のN型糖鎖結合活性の証明とそのシャペロン活性における役割.

    原田陽一郎、佐藤ちひろ、北島健:

    第7回関西グライコサイエンスフォーラム 

     詳細を見る

    開催年月日: 2006年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  55. 哺乳類細胞におけるデアミノノイラミン酸(KDN)代謝調節機構の解析

    郷 慎司、佐藤ちひろ、北島 健

    第26回 日本糖質学会年会 

     詳細を見る

    開催年月日: 2006年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  56. ウニ精子鞭毛局在flagellasialinのユニークな糖鎖修飾の精子運動性における重要性

    宮田真路, 佐藤ちひろ, 久美田紘信, 鳥山 優, 北島 健

    第77回日本動物学会大会 

     詳細を見る

    開催年月日: 2006年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  57. メダカ初期胚における糖鎖抗原3D11の発現と役割

    北島 健、原 弘明、足立朋子、佐藤ちひろ:

    第77回日本動物学会大会 

     詳細を見る

    開催年月日: 2006年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  58. Polysialic acid on microglia cell and its clearance after LPS-induced activation.

    Sialoglycoscience 2006 

     詳細を見る

    開催年月日: 2006年

    記述言語:英語   会議種別:口頭発表(招待・特別)  

    国名:日本国  

  59. Discovery of polysialic acid in microglia. Expression changes of α2,8-polysialyltransferses during activation of a mouse microglia cell line. 国際会議

    5th International Symposium on Glycosyltransferases 

     詳細を見る

    開催年月日: 2006年

    記述言語:英語   会議種別:ポスター発表  

    国名:日本国  

  60. ミクログリア細胞におけるポリシアル酸構造の存在.

    矢部宇一郎、北島 健、霜田 靖、渡邊 和忠 澤田 誠、佐藤ちひろ

    第78回日本生化学会大会 

     詳細を見る

    開催年月日: 2005年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  61. 新規ポリシアル酸含有糖タンパク質flagellasialinの発見、構造および機能.

    宮田真路, 佐藤ちひろ, 久美田紘信, 鳥山 優, Victor D. Vacquier, 北島 健

    第25回日本糖質学会 

     詳細を見る

    開催年月日: 2005年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  62. ジ・オリゴシアル酸を含有するマウス血清糖タンパク質の同定

    安川然太、佐藤ちひろ、北島 健

    第3回糖鎖科学名古屋拠点 若手の力 

     詳細を見る

    開催年月日: 2005年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  63. メダカ初期胚における細胞膜ラフト形成の重要性とその役割.

    足立朋子、佐藤ちひろ、北島 健

    第3回糖鎖科学名古屋拠点 若手の力 

     詳細を見る

    開催年月日: 2005年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  64. マウス乳糖タンパク質CD36上のポリシアル酸の乳腺発達段階における発現解析

    矢部宇一郎、佐藤ちひろ、北島 健

    日本農芸化学会2005年度大会 

     詳細を見る

    開催年月日: 2005年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  65. An essential role of carbohydrate-enriched membrane microdomains (rafts) in gastrulation of medaka fish, Oryzias latipes. 国際会議

    Gordon Research Conference on Glycobiology 

     詳細を見る

    開催年月日: 2005年

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  66. Milk CD36 Hannah Research Institute 国際会議

    Nagoya University Joint Workshop on Animal Biotechnology 

     詳細を見る

    開催年月日: 2005年

    記述言語:英語   会議種別:口頭発表(招待・特別)  

    国名:日本国  

  67. 糖タンパク質の多様なポリシアル酸修飾の意義を探る.

    佐藤ちひろ

    文科省特定領域研究 糖鎖によるタンパク質と分子複合体の機能調節 第三回夏期シンポジウム 

     詳細を見る

    開催年月日: 2005年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  68. Significance of membrane microdomains in the carbohydrate-dependent cell-cell interactions during early development of medaka fish.

    The 2nd Japan-The Netherlands Glycobiology Symposium. 

     詳細を見る

    開催年月日: 2005年

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  69. Biosynthesis and subcellular localiztion of deaminoneuraminic acid (KDN) in mammalian cells. 国際会議

    The 18th International Symposium on Glycoconjugates. 

     詳細を見る

    開催年月日: 2005年

    記述言語:英語   会議種別:ポスター発表  

  70. Demonstration of N-glycan-binding activity of HSP70 and its importance in the chaperoning activity.

    The 18th International Symposium on Glycoconjugates. 

     詳細を見る

    開催年月日: 2005年

    記述言語:英語   会議種別:ポスター発表  

  71. Development of a chemical method for detecting a unique sialic acid, cyclic neuraminic acid, in naturally-occurring sialyl glycoconjugates. 国際会議

    Pacifichem 

     詳細を見る

    開催年月日: 2005年

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  72. Chain length diversity of sialic acids and its biological significance

    Sato C.

    Trends in Glycoscience and Glycotechnology 

     詳細を見る

    開催年月日: 2004年9月

    記述言語:英語   会議種別:口頭発表(一般)  

    糖鎖末端には通常1残基のシアル酸が存在するが、そのシアル酸残基の上にさらに数残基のシアル酸が直鎖状に縮重合してシアル酸重合体を形成する場合がある。α2→8結合ジシアル酸 (重合度DP=2) 構造はガングリオシドの構成成分としてよく知られており、細胞接着、細胞分化、シグナル伝達、時期特異的発現など、多くの生物学的機能を果たしている。また重合度が8以上のポリシアル酸構造は神経細胞接着分子上に存在しており、発生や分化に関わることが知られている。しかし、重合度が2から7程度のジ・オリゴシアル酸構造をもつ糖タンパク質の存在や機能についてはこれまでほとんど注目されて来なかった。しかし近年、ジ・オリゴ・ポリシアル酸 (シアル酸重合体) 構造を微量検出する手法が改良され、天然にジ・オリゴ・ポリシアル酸含有糖タンパク質がこれまで知られている以上に数多く存在することが明らかにされてきている。そのため糖タンパク質上のシアル酸重合体構造が、既にガングリオシドにおいて明らかにされてきた機能の一端を担う可能性が、また従来考えられてきたこととは全く異なる新たな機能を担っていること、さらには新たなポリシアル酸の機能が明らかになってくるかもしれない。この総説ではシアル酸重合体の分析法、生合成、存在、機能における最近の知見を述べる。

    DOI: 10.4052/tigg.16.331

    Scopus

  73. Preface for the special issue entitled "new waves in sialobioscience"

    Sato C.

    Trends in Glycoscience and Glycotechnology 

     詳細を見る

    開催年月日: 2004年9月

    記述言語:英語   会議種別:口頭発表(一般)  

    DOI: 10.4052/tigg.16.291

    Scopus

  74. Occurrence of a novel 8-O-sulfated Neu5Ac-capped a2,8-linked polyNeu5Ac chains in the sea urchin sperm flagella glycoprotein

     詳細を見る

    開催年月日: 2004年

    記述言語:日本語   会議種別:ポスター発表  

    国名:日本国  

  75. Expression of the disialic acid structure on glycoproteins during T cell activation 国際会議

    Sialobiology 2004 

     詳細を見る

    開催年月日: 2004年

    記述言語:英語   会議種別:ポスター発表  

  76. Identification and characterization of a new heat shock protein-like lectin on the egg surface of sea urchin 国際会議

    21st International Lectin Meeting 

     詳細を見る

    開催年月日: 2004年

    記述言語:英語   会議種別:口頭発表(招待・特別)  

    国名:日本国  

  77. 動物細胞におけるシアル酸の取り込み、分解に関する研究

    郷慎司、佐藤ちひろ、北島健

    日本農芸化学会2004年度大会 

     詳細を見る

    開催年月日: 2004年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  78. ウニ卵局在精子結合タンパク質 (SBP)のレクチン活性

    原田陽一郎、佐藤ちひろ、北島健

    日本農芸化学会2004年度大会 

     詳細を見る

    開催年月日: 2004年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  79. 鳥類卵膜マトリクスの in vitro での再形成:糖タンパク質ZP1とZPCの特異的会合

    奥村裕紀、青木直人、佐藤ちひろ、灘野大太、松田幹

    日本農芸化学会2004年度大会 

     詳細を見る

    開催年月日: 2004年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  80. 食物抗原の腸管吸収:吸収された卵アルブミンの末梢血中での量的変動と質的変化

    松原 毅、青木直人、佐藤ちひろ、灘野大太、松田 幹

    日本農芸化学会2004年度大会 

     詳細を見る

    開催年月日: 2004年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  81. 膜リン脂質結合タンパク質MFG-E8の退縮期乳腺での発現変動

    中谷 肇、青山康二、青木直人、佐藤ちひろ、灘野大太、松田 幹

    日本農芸化学会2004年度大会 

     詳細を見る

    開催年月日: 2004年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  82. Study on the uptake of deaminoneuraminic acid (KDN) by mammalian cells

     詳細を見る

    開催年月日: 2004年

    記述言語:日本語   会議種別:ポスター発表  

    国名:日本国  

  83. Glycolipid- and phospholipid-binding activity of heat shock protein 70

     詳細を見る

    開催年月日: 2004年

    記述言語:日本語   会議種別:ポスター発表  

    国名:日本国  

  84. Roles of carbohydrate-mediated lipid raft-lipid raft interactions in early development of medaka, Oryzias latipes

     詳細を見る

    開催年月日: 2003年

    記述言語:日本語   会議種別:口頭発表(招待・特別)  

    国名:日本国  

  85. ジおよびオリゴシアル酸含有糖タンパク質の構造と機能

    佐藤ちひろ

    糖鎖科学名古屋拠点第1回「若手の力」フォーラム 

     詳細を見る

    開催年月日: 2003年

    記述言語:日本語   会議種別:口頭発表(招待・特別)  

    国名:日本国  

  86. シアル酸の重合度多様性の発見とその生物学的意義の解明

    佐藤ちひろ

    第24回日本糖質学会年会(奨励賞講演) 

     詳細を見る

    開催年月日: 2003年

    記述言語:日本語   会議種別:口頭発表(招待・特別)  

    国名:日本国  

  87. Discovery of two new polysialoglycoproteins in human and sea urchin. Linkage and length diversities of polysialic acid in animal glycoproteins. 国際会議

    Annual Conference of the Society for Glycobiology 

     詳細を見る

    開催年月日: 2003年

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  88. ヒトおよびマウスのミルクにオリゴ・ポリシアル酸構造が存在した

    矢部 宇一郎、佐藤ちひろ、松田 幹、北島 健

    日本農芸化学会2003年度大会 

     詳細を見る

    開催年月日: 2003年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  89. シアル酸合成能をもつ昆虫細胞の検索とその存在証明

    郷 慎司、佐藤ちひろ、池田素子、小林迪弘、松田 幹、北島 健

    日本農芸化学会2003年度大会; 

     詳細を見る

    開催年月日: 2003年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  90. ヒトミルクにおける新しいポリシアル酸含有糖タンパク質CD36の発見

    矢部宇一郎, 佐藤ちひろ, 松田 幹, 北島 健

    第24回日本糖質学会年会 

     詳細を見る

    開催年月日: 2003年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  91. 新規糖アミノ酸α-C-マンノシルトリプトファンの合成と生物機能解析

    西川俊夫、梶井重男、和田享子、石川 幸、磯部 稔、佐藤ちひろ、安川然太、北島 健

    第24回日本糖質学会年会; 

     詳細を見る

    開催年月日: 2003年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  92. ウニ精子鞭毛における新規ポリシアル酸含有糖タンパク質の発見とその糖鎖構造解析

    宮田真路, 佐藤ちひろ, 鳥山 優、北島 健

    第74回日本動物学会大会 

     詳細を見る

    開催年月日: 2003年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  93. メダカ初期胚発生における細胞膜マイクロドメイン形成の重要性の検討

    足立朋子、佐藤ちひろ、北島 健

     詳細を見る

    開催年月日: 2003年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  94. Characterization of a disialic acid-containing glycoprotein expressed on neural cells

     詳細を見る

    開催年月日: 2003年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  95. ジシアル酸含有糖タンパク質の神経細胞(Neuro2A)における発現

    佐藤ちひろ、松田 幹、北島 健

    第75回日本生化学会年会 

     詳細を見る

    開催年月日: 2002年

    記述言語:日本語   会議種別:ポスター発表  

    国名:日本国  

  96. ニジマスポリシアル酸転移酵素(PST)のcDNAクローニングと発現解析

    朝比奈慎二、佐藤ちひろ、松田 幹、北島 健

    日本農芸化学会2002年度大会 

     詳細を見る

    開催年月日: 2002年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  97. ニジマス卵巣におけるO-型糖鎖上のポリシアル酸構造の生合成に関与するシアル酸転移酵素のクローニング

    朝比奈慎二、松野みどり、佐藤ちひろ、北島 健

    第23回日本糖質学会年会 

     詳細を見る

    開催年月日: 2002年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  98. マンノース経口投与マウスの臓器におけるKDN合成

    郷 慎司、仲田大輔、佐藤ちひろ、松田 幹、北島 健

    日本農芸化学会2002年度大会 

     詳細を見る

    開催年月日: 2002年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  99. 精子膜マイクロドメインに局在する糖脂質と糖タンパク質に共通の糖鎖エピトープの機能

    宮田真路、前橋絵梨、太田薫、佐藤ちひろ、松田幹、北島 健

    第73回 日本動物学会年会 

     詳細を見る

    開催年月日: 2002年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  100. メダカ初期胚における細胞膜ドメイン(ラフト)の単離と細胞間相互作用における機能

    足立朋子、佐藤ちひろ、松田 幹、戸谷一英、村田健臣、碓氷泰一、北島 健

    第73回 日本動物学会年会 

     詳細を見る

    開催年月日: 2002年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  101. Sialic acid-mediated interactions at sea urchin 国際会議

    The Third Pan-Pacific Conference on Sialoglycoscience and Other Novel Forms of Glycosylation 

     詳細を見る

    開催年月日: 2002年

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  102. Sialic acid-dependent raft-raft interactions at fertilization 国際会議

    XVIth International Symposium on glycoconjugates 

     詳細を見る

    開催年月日: 2001年8月

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  103. Identification of a new diSia-containing glycoprotein (adipoQ) in bovine and mouse sera 国際会議

    XVIth International Symposium on Glycoconjugates 

     詳細を見る

    開催年月日: 2001年7月

    記述言語:英語   会議種別:ポスター発表  

    Congress Center The Hague Netherlands

  104. 哺乳動物に見いだされるオリゴ・ポリシアル酸含有糖タンパク質ファミリーの構造と機能

    佐藤ちひろ

    第43回FCCAセミナー 

     詳細を見る

    開催年月日: 2001年7月

    記述言語:日本語   会議種別:口頭発表(招待・特別)  

    "グランシップ, 静岡"

  105. "Identification of adipo Q, an adipocyte-specific glycoprotein, as a new oligosialic acid-containing glycoprotein and a possible substrate for the a2,8-sialyltransferase III (ST8SiaIII)." 国際会議

    "International Symposium on Protein Traffic, Glycosylation, and Human Health" 

     詳細を見る

    開催年月日: 2001年5月

    記述言語:英語   会議種別:ポスター発表  

  106. 精子ラフト-卵ラフト間相互作用の存在とその受精における重要性

    北島 健、前橋絵梨、太田 薫、佐藤ちひろ、松田 幹、鳥山 優

    日本動物学会第72回大会 

     詳細を見る

    開催年月日: 2001年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  107. ニジマス卵巣&#61537;2,6-シアル酸転移酵素のcDNAクローニングと組み換え体酵素の   性質

    朝比奈慎二、佐藤ちひろ、松田 幹、北島 健

    2001年度農芸化学大会 

     詳細を見る

    開催年月日: 2001年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  108. 血清糖タンパク質におけるジシアル酸およびオリゴシアル酸残基の 同定および生合成

    佐藤ちひろ、安川然太、本田直輝、松田 幹、北島 健

    第22回日本糖質学会年会 

     詳細を見る

    開催年月日: 2001年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  109. Roles of Membrane Microdomains (Rafts) in Sperm-Egg Interaction. 国際会議

    Second Canada-Japan Bilateral Workshop on Human Reproduction and Reproductive Biology 

     詳細を見る

    開催年月日: 2001年

    記述言語:英語   会議種別:口頭発表(招待・特別)  

    国名:日本国  

  110. 糖タンパク質糖鎖におけるジおよびオリゴシアル酸の構造と機能

    佐藤ちひろ

    糖鎖物質設計シンポジウム 

     詳細を見る

    開催年月日: 2000年8月

    記述言語:日本語   会議種別:口頭発表(招待・特別)  

    国名:日本国  

  111. "Expression and glycosylation of a major, carbohydrate-rich, cortical alveolus glycoprotein (hyosophorin) during oogenesis of medaka fish, Oryzias latipes" 国際会議

    3rd International Symposium of the Molecular and Cellular Biology of the Egg and Embryo 

     詳細を見る

    開催年月日: 2000年8月

    記述言語:英語   会議種別:ポスター発表  

  112. Di- and oligosialic acids as novel carbohydrate epitopes in leukocytes 国際会議

    7th Conference on human leukocyte differentiation antigens 

     詳細を見る

    開催年月日: 2000年6月

    記述言語:英語   会議種別:ポスター発表  

  113. Membrane microdomains are involved in carbohydrate-dependent sperm-egg interaction in sea urchin 国際会議

    3rd International Symposium of the Molecular and Cellular Biology of the Egg and Embryo 

     詳細を見る

    開催年月日: 2000年1月

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  114. 脂肪細胞の分化に伴うジおよびオリゴシアル酸含有糖タンパク質とα2,8-シアル酸 転移酵素の発現変化

    佐藤ちひろ、松田 幹、北島 健

    第73回日本生化学会大会 

     詳細を見る

    開催年月日: 2000年

    記述言語:日本語   会議種別:ポスター発表  

    国名:日本国  

  115. Lipid raft on gametic cells as a functional domain for sperm-egg interaction coupled with signal transduction 国際会議

    The International Symposium on Development and Fertilization of Sea Urchin and Marine Invertebrates 

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    開催年月日: 1999年12月

    記述言語:英語   会議種別:口頭発表(招待・特別)  

    国名:日本国  

  116. Egg receptor for sperm binds to gangliosides in the low density detergent-insoluble membrane (LD-DIM) domain of the sperm surface. Possible involvement of the LD-DIM in sperm-egg binding coupled with signal transduction during fertilization. 国際会議

    XVth International Symposium on Glycoconjugates 

     詳細を見る

    開催年月日: 1999年8月

    記述言語:英語   会議種別:ポスター発表  

    国名:日本国  

  117. Glycosphingolipid enriched microdomain on gametic cells as functional domain for sperm-egg interaction coupled with signal transduction 国際会議

    Gordon Research Conference on Fertilization and Activation of the Development 

     詳細を見る

    開催年月日: 1999年6月

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  118. 哺乳動物におけるオリゴシアル酸含有糖タンパク質の普遍的存在および分化に伴う発現変化

    佐藤ちひろ、松田 幹、北島 健

    第72回日本生化学会大会 

     詳細を見る

    開催年月日: 1999年

    記述言語:日本語   会議種別:ポスター発表  

    国名:日本国  

  119. オリゴシアル酸含有糖タンパク質の新しい化学的および免疫化学的解析法の開発と哺乳動物細胞における普遍的存在の証明

    "佐藤ちひろ,本田直輝,太田薫,福岡秀幸,井上貞子,松田幹,北島健"

    第71回日本生化学会大会 

     詳細を見る

    開催年月日: 1998年10月

    記述言語:日本語   会議種別:口頭発表(招待・特別)  

    国名:日本国  

  120. "Expression of a2,8-linked oligosialic acid-containing glycoproteins in mammalian cells, depending on development, cell differentiation, and overexpression of polysialyltransferase genes." 国際会議

    XIXth International Carbohydrate Symposium 

     詳細を見る

    開催年月日: 1998年8月

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  121. Frequent occurrence of oligosialyl units in vertebrate glycoproteins as evidenced by new chemical and immunochemical methods. 国際会議

    XIVth International Symposium on Glycoconjugates 

     詳細を見る

    開催年月日: 1997年9月

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  122. ブタ脳に存在するオリゴN-アセチルノイラミン酸含有糖タンパク質

    佐藤ちひろ、福岡秀幸、松田幹、井上貞子、井上康男、北島 健

    第70回日本生化学会大会 

     詳細を見る

    開催年月日: 1997年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  123. 哺乳動物細胞におけるオリゴ/ポリN-グリコリルノイラミン酸含有糖タンパク質の存在証明

    佐藤ちひろ、北島 健、古川清、井上貞子、井上康男

    第19回糖質シンポジウム 

     詳細を見る

    開催年月日: 1997年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  124. オリゴシアリル化は哺乳動物組織における糖タンパク質糖鎖の普遍的修飾反応である

    北島 健、佐藤ちひろ、福岡秀幸、松田幹、越野理香、小林一清、井上貞子、井上康男

    第19回糖質シンポジウム 

     詳細を見る

    開催年月日: 1997年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  125. 哺乳動物におけるKDN-およびpoly-α2,8-KDN含有複合糖質の免疫組織化学的および化学・生化学的同定とその生物学的意義

    井上貞子、北島 健、金森審子、佐藤ちひろ、Marti Ziak、Baoxi Qu、Xulei Zuo、Christian Zuber、Jurgen Roth、井上康男

    第18回糖質シンポジウム 

     詳細を見る

    開催年月日: 1996年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  126. α2→8-結合N-グリコリルノイラミン酸(Neu5Gc)オリゴマー構造を特異的に認識する単クローン抗体の調製と特異性の決定

    佐藤ちひろ、北島 健、井上康男、井上貞子

    第68回日本生化学会大会 

     詳細を見る

    開催年月日: 1995年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  127. Unique structures and structural chains of the cortical alveolar-derived glycopolyproteins in fish eggs upon fertilization and during early development. 国際会議

    3rd International Marine Biotechnology Conference 

     詳細を見る

    開催年月日: 1994年

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  128. 合成ポリシアロ糖脂質を用いたポリシアル酸微量検出法の開発

    佐藤ちひろ、北島 健、井上康男、井上貞子

    第66回日本生化学会大会 

     詳細を見る

    開催年月日: 1993年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  129. Diversity of polysialic acids structure in polysialoglycoproteins of Salmonidae fish eggs: Occurrence of α2→8-linked Poly(Neu5Ac), Poly(Neu5Gc), Poly(KDN), Poly(Neu5Ac,Neu5Gc), and their partially O-acetylated derivatives. 国際会議

    International Symposium on Polysialic Acid 

     詳細を見る

    開催年月日: 1992年8月

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  130. Polysialic acids in animals. 国際会議

    6th the Federation of Asian and Oceanian Biochemists Congress 

     詳細を見る

    開催年月日: 1992年

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  131. ポリシアロ糖タンパク質における α2→8 結合ポリシアル酸構造の多様性

    佐藤ちひろ、北島 健、田沢一朗、井上康男、井上貞子

    第65回日本生化学会大会 

     詳細を見る

    開催年月日: 1992年

    記述言語:日本語   会議種別:口頭発表(一般)  

    国名:日本国  

  132. Sialic acid-dependent raft-raft interactions at fertilization

    K. Ohta, E. Maehashi, C. Sato, S. Miyata, M. Toriyama, T. Matsuda, N. Hirohashi, K. Kitajiama

    XVIth International Symposium on glycoconjugates  2001年8月19日 

     詳細を見る

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  133. オリゴシアル酸含有糖タンパク質の新しい化学的および免疫化学的解析法の開発と哺乳動物細胞における普遍的存在の証明 国際会議

    佐藤ちひろ, 本田直輝, 太田薫, 福岡秀幸, 井上貞子, 松田幹, 北島健

    第71回日本生化学会大会  1998年10月16日 

     詳細を見る

    記述言語:日本語   会議種別:口頭発表(招待・特別)  

  134. Preface for the special issue entitled "new waves in sialobioscience" 国際会議

    Sato C

    Trends in Glycoscience and Glycotechnology  2004年9月  Trends in Glycoscience and Glycotechnology

     詳細を見る

    記述言語:英語   会議種別:口頭発表(一般)  

  135. Polysialic acid is not a negative regulator any longer in neurogenesis and neuronal functions: A new finding of its binding to a particular group of neurotransmitters.

    Ken Kitajima, Ryo Isomura, Chihiro Sato

    Gordon Research Conference on Glycobiology,  2009年1月18日 

     詳細を見る

    記述言語:英語   会議種別:ポスター発表  

  136. One-pot Enzymatic Synthesis of CMP-[14C]deaminoneuraminic Acid (KDN).

    Yuko Nakajima, Akiko Fujita, Chihiro Sato, Ken Kitajima

    SialoGlyco Conference 2008  2008年7月 

     詳細を見る

    記述言語:英語   会議種別:ポスター発表  

  137. Occurrence of the Cyclic Sialic Acid in Mammalian Cells and Tissues As Demonstrated by Chemical Methods.

    K. Kitajima, S.Iwata, N. Kawakami, C. Sato, H. Ando, H. Ohno, H. Ishida, M. Kiso, O. Taguchi, R. Kannagi

    SialoGlyco Conference 2008  2008年7月 

     詳細を見る

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  138. Novel insights into the novel binding sites of the sialic acid biding Ig-like lectin-7 (Siglec-7) gained by in silico docking studies.

    Nao Yamakawa, Chihiro Sato, Ken Kitajima

    A one-day symposium on Sialyltransferases, Functional Glycomics, and Genomics of Zebrafish,  2008年11月18日 

     詳細を見る

    記述言語:英語   会議種別:シンポジウム・ワークショップ パネル(指名)  

  139. Membrane microdomains are involved in carbohydrate-dependent sperm-egg interaction in sea urchin

    K. Ohta, C. Sato, E. Maehashi, T. Matsuda, M. Toriyama, N. Hirohashi, W.J. Lennarz, K. Kitajima

    3rd International Symposium of the Molecular and Cellular Biology of the Egg and Embryo  2000年1月1日 

     詳細を見る

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  140. mAb.A2B5の抗原特異性の決定とマウス脳発達段階におけるmAb.A2B5反応性オリゴシアル酸含有糖タンパク質の発現解析

    猪子恵未, 西浦祐二, 田中浩士, 高橋孝志, 北島健, 佐藤ちひろ

    第81回日本生化学会大会  2008年12月9日 

     詳細を見る

    記述言語:英語   会議種別:ポスター発表  

  141. Lipid raft on gametic cells as a functional domain for sperm-egg interaction coupled with signal transduction

    K. Ohta, C. Sato, T. Matsuda, M. Toriyama, V. D. Vacquier, N. Hirohashi, W. J. Lennarz, K. Kitajima

    The International Symposium on Development and Fertilization of Sea Urchin and Marine Invertebrates  1999年12月1日 

     詳細を見る

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  142. In vitro and in silico docking studies of heat shock protein (Hsp) 70 with sulfatide.

    Nao Yamakawa, Yoichiro Harada, Chihiro Sato, Gerard Vergoten, Ken Kitajima

    24th International Carbohydrate Symposium,  2008年7月27日 

     詳細を見る

    記述言語:英語   会議種別:ポスター発表  

  143. In silico binding studies predict novel sialic acid binding sites on the sialic acid binding Ig-like lectin-7 (Siglec-7)

    Nao Yamakawa, Chihiro Sato, Paul R. Crocker, Gérard Vergoten, Ken Kitajima: I

    SialoGlyco Conference 2008  2008年7月 

     詳細を見る

    記述言語:英語   会議種別:ポスター発表  

  144. Identification of the nuclear export signals that regulate the intracellular localization of the mouse CMP-sialic acid synthetase.

    Akiko Fujita, Chihiro Sato, Ken Kitajima

    SialoGlyco Conference 2008  2008年7月 

     詳細を見る

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  145. Identification of a new diSia-containing glycoprotein (adipoQ) in bovine and mouse sera

    C. Sato, Z. Yasukawa, N. Honda, T. Matsuda, K. Kitajima

    XVIth International Symposium on Glycoconjugates  2001年7月19日 

     詳細を見る

    記述言語:英語   会議種別:ポスター発表  

    Congress Center The Hague Netherlands

  146. Glycosphingolipid enriched microdomain on gametic cells as functional domain for sperm-egg interaction coupled with signal transduction

    K. Ohta, C. Sato, T. Matsuda, M. Toriyama, V. D. Vacquir, N. Hirohashi, W. J. Lennarz, K. Kitajima

    Gordon Research Conference on Fertilization and Activation of the Development  1999年6月1日 

     詳細を見る

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  147. Frequent occurrence of oligosialyl units in vertebrate glycoproteins as evidenced by new chemical and immunochemical methods.

    C. Sato, H. Fukuoka, N. Honda, T. Matsuda, R. Koshino, K. Kobayashi, S. Inoue, Y. Inoue, K. Kitajima

    XIVth International Symposium on Glycoconjugates  1997年9月27日 

     詳細を見る

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  148. Egg receptor for sperm binds to gangliosides in the low density detergent-insoluble membrane (LD-DIM) domain of the sperm surface. Possible involvement of the LD-DIM in sperm-egg binding coupled with signal transduction during fertilization.

    K. Ohta, C. Sato, T. Matsuda, N. Hirohashi, W. J. Lennarz, K. Kitajima

    XVth International Symposium on Glycoconjugates  1999年8月1日 

     詳細を見る

    記述言語:英語   会議種別:ポスター発表  

  149. Di- and oligosialic acids as novel carbohydrate epitopes in leukocytes

    K. Kitajima, C. Sato

    7th Conference on human leukocyte differentiation antigens  2000年6月1日 

     詳細を見る

    記述言語:英語   会議種別:ポスター発表  

  150. Complex formation between polysialic acid and brain derived neurotrophic factor (BDNF).

    Chihiro Sato, Yukihiro Kanato, Ken Kitajima

    24th International Carbohydrate Symposium,  2008年7月27日 

     詳細を見る

    記述言語:英語   会議種別:ポスター発表  

  151. Chain length diversity of sialic acids and its biological significance 国際会議

    Sato C

    Trends in Glycoscience and Glycotechnology  2004年9月  Trends in Glycoscience and Glycotechnology

     詳細を見る

    記述言語:英語   会議種別:口頭発表(一般)  

    糖鎖末端には通常1残基のシアル酸が存在するが、そのシアル酸残基の上にさらに数残基のシアル酸が直鎖状に縮重合してシアル酸重合体を形成する場合がある。α2→8結合ジシアル酸 (重合度DP=2) 構造はガングリオシドの構成成分としてよく知られており、細胞接着、細胞分化、シグナル伝達、時期特異的発現など、多くの生物学的機能を果たしている。また重合度が8以上のポリシアル酸構造は神経細胞接着分子上に存在しており、発生や分化に関わることが知られている。しかし、重合度が2から7程度のジ・オリゴシアル酸構造をもつ糖タンパク質の存在や機能についてはこれまでほとんど注目されて来なかった。しかし近年、ジ・オリゴ・ポリシアル酸 (シアル酸重合体) 構造を微量検出する手法が改良され、天然にジ・オリゴ・ポリシアル酸含有糖タンパク質がこれまで知られている以上に数多く存在することが明らかにされてきている。そのため糖タンパク質上のシアル酸重合体構造が、既にガングリオシドにおいて明らかにされてきた機能の一端を担う可能性が、また従来考えられてきたこととは全く異なる新たな機能を担っていること、さらには新たなポリシアル酸の機能が明らかになってくるかもしれない。この総説ではシアル酸重合体の分析法、生合成、存在、機能における最近の知見を述べる。

  152. Brain-derived neurotrophic factor binds to polysialic acid directly depending on degree of polymerization.

    Yukihiro Kanato, Ken Kitajima, Chihiro Sato

    SialoGlyco Conference 2008  2008年7月 

     詳細を見る

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  153. "Identification of adipo Q, an adipocyte-specific glycoprotein, as a new oligosialic acid-containing glycoprotein and a possible substrate for the a2,8-sialyltransferase III (ST8SiaIII)."

    C. Sato, Z. Yasukawa, N. Honda, T. Matsuda, K. Kitajima

    "International Symposium on Protein Traffic, Glycosylation, and Human Health"  2001年5月12日 

     詳細を見る

    記述言語:英語   会議種別:ポスター発表  

  154. "Expression of a2,8-linked oligosialic acid-containing glycoproteins in mammalian cells, depending on development, cell differentiation, and overexpression of polysialyltransferase genes."

    K. Kitajima, C. Sato, N. Honda, T. Matsuda, M. Hara-Yokoyama, B. Close, K. J. Colley

    XIXth International Carbohydrate Symposium  1998年8月1日 

     詳細を見る

    記述言語:英語   会議種別:口頭発表(招待・特別)  

  155. "Expression and glycosylation of a major, carbohydrate-rich, cortical alveolus glycoprotein (hyosophorin) during oogenesis of medaka fish, Oryzias latipes"

    K. Kitajima, J. Taniguchi, C. Sato, M. Kageyama, N. Aoki, T. Matsuda

    3rd International Symposium of the Molecular and Cellular Biology of the Egg and Embryo  2000年8月1日 

     詳細を見る

    記述言語:英語   会議種別:ポスター発表  

  156. 魚類CMP-シアル酸合成酵素の構造と性質 国際会議

    藤田明子, 安川裕子, 佐藤ちひろ, 北島健

    日本農芸化学会2009年度大会  2009年3月29日 

     詳細を見る

    記述言語:日本語   会議種別:口頭発表(一般)  

  157. 酸性多糖と神経栄養因子との相互作用解析.

    金戸幸弘, 北島健, 佐藤ちひろ

    第81回日本生化学会大会  2008年12月9日 

     詳細を見る

    記述言語:英語   会議種別:口頭発表(一般)  

  158. 糖タンパク質糖鎖におけるジおよびオリゴシアル酸の構造と機能 国際会議

    佐藤ちひろ

    糖鎖物質設計シンポジウム  2000年8月1日 

     詳細を見る

    記述言語:日本語   会議種別:口頭発表(招待・特別)  

  159. 昆虫細胞由来シアル酸9-リン酸合成酵素の構造と基質特異性の解析 国際会議

    濱口香代, 郷慎司, 佐藤ちひろ, 小林迪弘, 池田素子, 北島健

    第81回日本生化学会大会  2008年12月9日 

     詳細を見る

    記述言語:日本語   会議種別:ポスター発表  

  160. 抗ジシアル酸抗体が認識する急性期タンパク質の同定.

    安川然太, 北島健, 佐藤ちひろ

    第81回日本生化学会大会  2008年12月9日 

     詳細を見る

    記述言語:英語   会議種別:ポスター発表  

  161. 哺乳類シアロ糖タンパク質のデアミノノイラミン酸 (KDN) 修飾糖タンパク質への改変. 国際会議

    中島優子, 藤田明子, 佐藤ちひろ, 北島健

    第81回日本生化学会大会  2008年12月9日 

     詳細を見る

    記述言語:日本語   会議種別:ポスター発表  

  162. 哺乳動物に見いだされるオリゴ・ポリシアル酸含有糖タンパク質ファミリーの構造と機能 国際会議

    佐藤ちひろ

    第43回FCCAセミナー  2001年7月14日 

     詳細を見る

    記述言語:日本語   会議種別:口頭発表(招待・特別)  

    "グランシップ, 静岡"

  163. 化学的検出法を用いた天然におけるサイクリックシアル酸の局在検索. 国際会議

    岩田章子, 佐藤ちひろ, 安藤弘宗, 石田秀治, 木曽真, 神奈木玲児, 北島健

    第81回日本生化学会大会  2008年12月9日 

     詳細を見る

    記述言語:日本語   会議種別:ポスター発表  

  164. ラクタム化シアル酸誘導体の合成とその分解反応に関する研究. 国際会議

    大野ひろみ, 安藤弘宗, 川上信彦, 岩田章子, 佐藤ちひろ, 北島健, 石田秀治, 木曽真

    日本農芸化学会2009年度大会  2009年3月29日 

     詳細を見る

    記述言語:日本語   会議種別:ポスター発表  

  165. ポリシアル酸は特定の神経伝達物質と相互作用する.

    磯村遼, 北島健, 佐藤ちひろ

    第81回日本生化学会大会  2008年12月9日 

     詳細を見る

    記述言語:日本語   会議種別:口頭発表(一般)  

  166. ポリシアル酸の新機能 国際会議

    佐藤ちひろ

    第6回日本糖鎖科学コンソーシアムシンポジウム-糖鎖研究と他領域との統合-  2008年12月3日 

     詳細を見る

    記述言語:日本語   会議種別:シンポジウム・ワークショップ パネル(指名)  

  167. ポリシアル酸と脳由来神経栄養因子の相互作用の解析 国際会議

    金戸幸弘, 北島健, 佐藤ちひろ

    日本農芸化学会2009年度大会  2009年3月29日 

     詳細を見る

    記述言語:日本語   会議種別:口頭発表(一般)  

  168. ポリシアル酸とFGF-2の相互作用の解析. 国際会議

    小野明日香, 金戸幸弘, 北島 健, 佐藤ちひろ

    日本農芸化学会2009年度大会  2009年3月29日 

     詳細を見る

    記述言語:日本語   会議種別:ポスター発表  

▼全件表示

Works(作品等) 14

  1. Specific labeling and chemical analysis of sialic acid and sialyloligo/polymers

    2011年

     詳細を見る

    発表場所:Glycoscience protocol on line database (GlycoPOD)  

  2. Enzyme assay of polysialyltransferase (

    2011年

     詳細を見る

    発表場所:glycopod  

  3. Carbohydrate analysis by gas-liquid chromatography

    2011年

  4. Enzyme assay of polysialyltransferase (

    2011年

     詳細を見る

    発表場所:glycopod  

  5. Carbohydrate analysis by gas-liquid chromatography

    2011年

     詳細を見る

    発表場所:Glycopod  

  6. Specific labeling and chemical analysis of sialic acid and sialyloligo/polymers

    2011年

     詳細を見る

    発表場所:Glycoscience protocol on line database (GlycoPOD)  

  7. シアル酸と進化

    2006年

     詳細を見る

    発表場所:グライコワード:http://www.gak.co.jp/FCCA/glycoword/ESA03/ES-A03J.html  

  8. シアル酸と進化

    2006年

     詳細を見る

    発表場所:グライコワード:http://www.gak.co.jp/FCCA/glycoword/ESA03/ES-A03J.html  

  9. 神経系におけるポリシアル酸の役割

    2004年

     詳細を見る

    発表場所:グライコワード:http://www.gak.co.jp/FCCA/glycoword/NSA03/NS-A03J.html  

  10. 神経系におけるポリシアル酸の役割

    2004年

     詳細を見る

    発表場所:グライコワード:http://www.gak.co.jp/FCCA/glycoword/NSA03/NS-A03J.html  

  11. 糖鎖生物学

    2003年

     詳細を見る

    翻訳(一部)

  12. 糖鎖生物学

    2003年

     詳細を見る

    翻訳(一部)

  13. オリゴ・ポリシアル酸の生合成

    2002年

     詳細を見る

    発表場所:グライコワード:http://www.gak.co.jp/FCCA/glycoword/GPB04/GPB04J.html  

  14. オリゴ・ポリシアル酸の生合成

    2002年

     詳細を見る

    発表場所:グライコワード:http://www.gak.co.jp/FCCA/glycoword/GPB04/GPB04J.html  

▼全件表示

共同研究・競争的資金等の研究課題 4

  1. ポリシアル酸と相互作用する分子の解明

    2010年4月 - 2011年3月

    公益信託 林女性自然科学研究者研究助成基金 

      詳細を見る

    資金種別:競争的資金

  2. 脳機能に関わるシアル酸重合体と相互作用する分子の同定とその応用基盤の確立

    2007年4月

    加藤記念研究助成 

      詳細を見る

    資金種別:競争的資金

  3. ミクログリア細胞におけるポリシアル酸の存在とその機能解析

    2006年

  4. 神経形成を制御する新規糖鎖オリゴシアル酸の作用機構の解明

    2003年4月 - 2004年3月

    水谷科学振興財団2003年度研究助成 

      詳細を見る

    資金種別:競争的資金

科研費 29

  1. 免疫細胞レクチンシグレックの新規リガンド結合部位の証明と新しい免疫制御機構の解明

    研究課題/研究課題番号:21H02425  2021年4月 - 2025年3月

    文部科学省  科研費  B

      詳細を見る

    担当区分:研究代表者  資金種別:競争的資金

  2. 脊椎動物におけるシアル酸特異的硫酸転移酵素群の発見とその生物学的重要性の証明

    研究課題/研究課題番号:22H02256  2022年4月 - 2025年3月

    科学研究費助成事業  基盤研究(B)

    北島 健, 佐藤 ちひろ, 呉 迪, 羽根 正弥

      詳細を見る

    担当区分:研究分担者 

    糖鎖付加はタンパク質および脂質に対する主要な修飾反応である。その糖鎖の最末端は通常シアル酸が占めており、細胞認識や細胞接着を媒介・制御している。しかし、そのシアル酸が更に硫酸化やアセチル化修飾されている事実は殆ど知られておらず、その修飾シアル酸の存在意義も不明である。近年、我々はシアル酸の修飾の中でも脊椎動物に普遍的に存在する硫酸化に着目して、その生合成酵素であるシアル酸硫酸転移酵素遺伝子を少なくとも2種類同定した。またそれらの遺伝子ノックアウトメダカが幼魚段階で致死となることを明らかにした。本研究は、これらの研究結果に基づいてシアル酸の硫酸化の生物学的意義の解明を目指す

  3. ポリシアル酸による新しい細胞機能調節機構の分子基盤の解明

    研究課題/研究課題番号:15K06995  2015年4月 - 2018年3月

    佐藤 ちひろ

      詳細を見る

    担当区分:研究代表者 

    配分額:4940000円 ( 直接経費:3800000円 、 間接経費:1140000円 )

    脊椎動物脳には学習・記憶・社会性行動に深くかかわる酸性多糖"ポリシアル酸(polySia, PSA)"が存在する。我々はこれまでpolySia がその機能を発揮する際、従来考えられてきた反接着性相互作用を持つ"反発性の場"をつくりだしているだけでなく、神経作用因子の保持および放出(提示)作用を持つ"誘因性の場"も提示することを世界に先駆けて明らかにしてきた。本研究では、我々が明らかにしてきたpolySia の”誘因性の場”に着目し、神経作用因子の保持メカニズムをpolySia鎖の構造や相互作用モードをその生合成酵素と共に検証した。

  4. 合成ジ・オリゴシアル酸プローブを用いる自然免疫システムの解明と制御

    研究課題/研究課題番号:26282209  2014年4月 - 2017年3月

    日本学術振興会  科学研究費助成事業 基盤研究(B)  基盤研究(B)

    田中 浩士, 山口 芳樹, 佐藤 ちひろ, 山口 芳樹, 佐藤 ちひろ

      詳細を見る

    担当区分:研究分担者 

    本研究は、まず、7,8位に遊離水酸基を有するシアル酸糖供与体が非アセトニトリル溶媒中で高いα選択的グリコシル化が進行することを明らかにした。さらに、ジシアル酸を有するアレンモノマーのニッケル触媒を用いる重合により、狭い分子量分布を有する糖鎖高分子の合成を達成した。その糖鎖高分子は、Siglec-7とGD3との相互作用を阻害できることを見出した。さらに、デキストランにジシアル酸ユニットを結合させたプローブが、より低濃度でそれら相互作用を阻害できることを明らかにした。今後は、これらのプローブの細胞への影響を精査していく予定である。

  5. 精神疾患に関与するポリシアル酸転移酵素の機能解析

    研究課題/研究課題番号:26110708  2014年4月 - 2016年3月

    新学術領域研究(研究領域提案型)

    佐藤 ちひろ

      詳細を見る

    担当区分:研究代表者 

    配分額:9360000円 ( 直接経費:7200000円 、 間接経費:2160000円 )

    本研究は統合失調症などの精神疾患に関連するポリシアル酸転移酵素ST8SIA2の機能解析が目的であり、本研究では報告のある精神疾患患者に有意なSNPsや変異に関して、それらの酵素がもたらす産物であるポリシアル酸の構造および機能解析を行った。具体的にはプロモーターに存在するrSNPに関してはプロモータ解析および遺伝子のマイクロアレイの解析を各種細胞を用いて行い、ある転写因子によって細胞特異的にST8SIA2の発現異常が起こる可能性を示した。翻訳領域に存在しアミノ酸置換を伴うSNPの解析から、疾患型が合成するポリシアル酸が損なわれ、特にBDNFの結合やproBDNFの結合性が正常型より損なわれることがわかった。また翻訳領域に存在しアミノ酸置換を伴わないsSNPは、コドン使用頻度によりST8SIA2の翻訳速度が変化し、ポリシアル酸の生合成に影響を与える可能性が示唆された。イントロンに存在するiSNPは、特に双極性障害型のSNPに関して、マウスの神経細胞およびヒトHEK細胞においてST8SIA2の合成が促進され、polySiaが過剰発現することが明らかになった。ST8SIA2の過剰発現の影響を調べるために子宮内エレクトロポレーション法により、ST8SIA2およびST8SIA4の遺伝子導入を行ったところ、ニューロンの移動がMockに比べて変化した。以上のことより、ST8SIA2遺伝子発現は細胞特異的に発現が厳密に制御されており、それに伴いpolySiaの構造が損なわれることが分かった。つまり、polySia構造は厳密に構造が制御されており、それによって神経作用因子であるBDNF、FGF2, proBDNFの結合性を制御することなどで、正常な神経機能を果たすことが考えられた。
    27年度が最終年度であるため、記入しない。
    27年度が最終年度であるため、記入しない。

  6. 精神疾患に関与するポリシアル酸転移酵素の機能解析

    2014年4月 - 2016年3月

    科学研究費助成事業  新学術領域

    佐藤ちひろ

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    担当区分:研究代表者  資金種別:競争的資金

  7. 精子膜マイクロドメイン局在糖鎖による新規細胞内カルシウムイオン調節機構の解明

    研究課題/研究課題番号:25292216  2013年4月 - 2016年3月

    北島 健

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    担当区分:研究分担者 

    受精における糖鎖の重要性は多数の報告があるが、遺伝子改変動物の解析結果から受精の成立には必ずしも必須ではない場合があることが例証されるなど、現在、糖鎖が関わる受精の分子機構の再評価が課題である。その課題解決のために、我々は糖鎖が集積してタンパク質や脂質とともに形成する分子複合体「細胞膜マイクロドメイン」に着目して研究を行った。本研究では、精子マイクロドメインに局在し糖鎖に富むGPI-アンカー分子が、これまで見出されていたウニと哺乳類以外にも、鳥類、両生類にも存在することを明らかにした。また、これらの分子が糖鎖を介して細胞内Caイオン調節に関わることを証明した。

  8. 微小糖鎖空間における酸性多糖が織りなす神経制御機構の解明

    2012年4月 - 2014年3月

    科学研究費補助金  新学術領域

    佐藤ちひろ

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    担当区分:研究代表者 

  9. 細胞表面酸性多糖が織りなす微小糖鎖空間による神経機能調節機構の解明

    研究課題/研究課題番号:24110506  2012年4月 - 2014年3月

    新学術領域研究(研究領域提案型)

    佐藤 ちひろ

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    担当区分:研究代表者 

    配分額:7150000円 ( 直接経費:5500000円 、 間接経費:1650000円 )

    ポリシアル酸はシアル酸が8-400残基縮重合した構造の総称で、胎児脳の神経細胞接着分子(NCAM)を特異的に修飾する。成体脳ではその大部分が消失するが、海馬や嗅球といった神経新生の盛んな領域に発現が継続している。ポリシアル酸の機能として反接着作用が知られていたが、我々はポリシアル酸が自身に神経機能を制御する分子、BDNF、FGF2,ドーパミンなどを結合し、その機能を制御しうることを明らかにしてきている。本研究では、(1) polySiaによる神経作用因子の保持・放出機構の解明、(2) poySiaの"質と量"を制御する生合成機構の解明、(3) polySiaと統合失調症などの精神疾患との関わりの解明をすすめること目指した。(1)に関してはpolySiaが、自身の質と量を調節することにより、神経作用因子を保持状態を制御することがわかった。またその受容体への受け渡し機構には、より高親和性受容体への直接受け渡し、共受容体への間接的な受け渡し、polySia鎖の構造変化による受け渡しなど、さまざまな機構が働いていることが初めて明らかになった。(2)では、polySiaの質と量を制御する機構としてポリシアル酸転移酵素(ST8SIA2)に着目し、その変異が生合成する機構を一部明らかにした。(3)においては、統合失調症患者で明らかになったST8SIA2のSNP-7およびSNP-9の解析を正常型とあわせて行うことにより、その生合成酵素の産物の不全がpolySia鎖の不全を引き起こし、ひいては分子結合性における不全がおきることによるシグナル伝達の不具合がおこることを示した。以上の結果より、本研究において、polySia鎖がつくり出す細胞膜近傍における空間において、自身の分子結合性により細胞機能を制御していること、このpolySia鎖の生合成は高度の制御されていることが強く示唆された。
    25年度が最終年度であるため、記入しない。
    25年度が最終年度であるため、記入しない。

  10. 微小糖鎖空間における酸性多糖が織りなす神経制御機構の解明

    2012年4月 - 2014年3月

    科学研究費助成事業  新学術領域

    佐藤ちひろ

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    担当区分:研究代表者  資金種別:競争的資金

  11. ポリシアル酸とFGF2による神経機能の新しい制御メカニズムの証明

    研究課題/研究課題番号:23570133  2011年 - 2013年

    佐藤 ちひろ

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    担当区分:研究代表者 

    配分額:5460000円 ( 直接経費:4200000円 、 間接経費:1260000円 )

    ポリシアル酸(polySia)はシアル酸が8-400残基縮重合した構造体の総称で、胎児脳の神経細胞接着分子(NCAM)を修飾している。成体脳ではpolySia構造はほとんど消失するが、海馬や嗅球などの神経新生が盛んな領域ではその発現が維持されている。NCAM上のpolySia構造はその巨大な排除体積によって、細胞接着を負に制御することが知られていたが、本研究によりpolySiaはFGF2などの神経における生理活性物質を自身に保持する分子保持機能を持つこと、またその受容体への提示を制御することで神経機能を制御しうることが示された。この機能はpolySiaの構造によって調節されることも示唆された。

  12. 昆虫特異的シアル酸の発見と代謝経路の解明

    研究課題/研究課題番号:23658287  2011年 - 2012年

    北島 健

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    担当区分:研究分担者 

    脊椎動物において共通にみられる通常のシアル酸は、実は昆虫には存在せず、むしろ昆虫型シアル酸というべきユニークな構造単位が存在するのではないかという仮説をたて、その検証に取り組んだ。ショウジョウバエの他、コクヌストモドキとガに着目して、昆虫型シアル酸の精製、構造解析、存在分布、代謝経路の解明をおこなった。その結果、昆虫型シアル酸というべき構造の存在が示された。この構造は、本研究で調べた昆虫すべてに共通に存在した。一方、シアル酸代謝酵素遺伝子はすべての昆虫に存在するわけではないこと、また存在する種でも、通常のシアル酸に対する活性は消失する傾向にあることがわかった。今後、これらの代謝酵素が昆虫型シアル酸を基質とするかどうかの調査が急務であるが、以上のことから、昆虫には、通常のシアル酸ではなく昆虫型シアル酸が存在するという仮説がほぼ検証された。

  13. 初期胚表面に存在する巨大糖鎖の機能とその分子機構の解明

    研究課題/研究課題番号:22380187  2010年 - 2012年

    北島 健

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    担当区分:研究分担者 

    初期胚表層にどうして巨大糖鎖が存在するのかという疑問の解決を目指して研究を行って、新しい知見を得た。まず、巨大糖鎖をもつ糖タンパク質 LeX-gp について、その精製に成功、その糖鎖が細胞接着性に関わる LeX構造のタンデム反復構造という新規構造をもつことを明らかにした。つぎに、受精時に卵から囲卵腔中に分泌される hyosophorin について、そのペプチド部分が細胞表面の特異的な受容体を介して細胞増殖促進活性を示すこと、糖鎖部分は受精時の卵表層反応の進行に重要であることを明らかにした。本研究成果を通じて、巨大糖鎖は細胞表面と相互作用して細胞表層の性質を変化させ、細胞の命運を決定するという仮説を提唱したい。

  14. 脳に局在するポリシアル酸構造と脳由来神経栄養因子との相互作用の解析

    研究課題/研究課題番号:20570107  2008年 - 2010年

    佐藤 ちひろ

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    担当区分:研究代表者 

    配分額:4810000円 ( 直接経費:3700000円 、 間接経費:1110000円 )

    ポリシアル酸は脊椎動物脳において発現する酸性多糖である。特に、胎児期のNCAMを修飾しており、その巨大な排除体積により、細胞-細胞/細胞外マトリックスの相互作用において負の制御を司る分子としてこれまで考えられてきた。本研究ではポリシアル酸が、負の相互作用をもつだけでなく、脳由来神経栄養因子(BDNF)という脳内の生理活性分子と直接相互作用すること、つまり正の相互作用を通じて、その受容体への結合を制御する機構の存在を初めて明らかにした。

  15. 脳に局在するポリシアル酸構造と脳由来神経栄養因子との相互作用の解析       

    2008年

    科学研究費補助金  基盤研究(C),課題番号:20570107

    佐藤 ちひろ

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    担当区分:研究代表者 

  16. 脳に局在するポリシアル酸構造と脳由来神経栄養因子との相互作用の解析

    2008年

    科学研究費助成事業  基盤研究(C),課題番号:20570107

    佐藤 ちひろ

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    担当区分:研究代表者  資金種別:競争的資金

  17. 動物精子表面糖鎖による新しい受精能制御の分子機構の解明

    研究課題/研究課題番号:19380192  2007年 - 2009年

    北島 健

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    担当区分:研究分担者 

    精子受精能を制御する精子表面糖鎖の役割解明を目指して、二つの研究計画を遂行して新しい知見を得た。まず、ブタおよびウニの精子鞭毛に糖鎖に富む膜糖タンパク質を発見し、その糖タンパク質が精子細胞内のカルシウム濃度を制御することで運動性を抑制することを明らかにした。つぎに、ブタ精子表面に強固に付着する精漿由来の高糖含有糖タンパク質を発見し、その糖タンパク質が受精能獲得時に精子表面から脱離することによって受精能が高まることを見いだした。

  18. ミクログリア細胞におけるポリシアル酸の存在とその機能解析

    2006年4月 - 2008年3月

    科学研究費補助金  若手研究(B)

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    担当区分:研究代表者 

  19. ミクログリア細胞におけるポリシアル酸の存在とその機能解析

    2006年4月 - 2008年3月

    日本学術振興会  科学研究費助成事業  若手研究(B)

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    資金種別:競争的資金

  20. ミクログリア細胞におけるポリシアル酸の存在とその機能解析

    研究課題/研究課題番号:18770083  2006年 - 2007年

    佐藤 ちひろ

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    担当区分:研究代表者 

    配分額:3700000円 ( 直接経費:3700000円 )

    ポリシアル酸はシアル酸重合体の総称であり、魚卵糖タンパク質(PSGP)や神経細胞接着分子(NCAM)にその存在が知られている。ポリシアル酸の機能は、NCAMを中心に解析が進んでおり、かさ高い排除体積とポリアニオニックな性質による反接着作用を持つことが知られている。我々はこのミクログリア細胞に注目してポリシアル酸の存在検索および発現解析を行い、ミクログリア細胞株Ra2におけるポリシアル酸の存在をポリシアル酸に特異的な抗体12E3および特異的な酵素Endo-Nを用いて証明した。またRa2細胞に対してLPS刺激を行うとポリシアル酸が完全に消失することを見出した。またRa2細胞のLPS刺激によるポリシアル酸構造消失の分子機構を明らかにするために、分解過程に注目して実験を行った。シアル酸の分解に関わる酵素としてシアリダーゼに着目し、まず、シアリダーゼ遺伝子(Neu)の発現解析を行った。その結果、Neu2とNeu4が活性化により変動していることが分かった。さらに、実際にシアリダーゼ活性がポリシアル酸の消失に関わっていることを明らかにするために、シアリダーゼ阻害剤存在下でLPS刺激を行い、細胞表面のポリシアル酸の存在を調べた。同時に培地におけるシアリダーゼ活性を測定した。その結果、ポリシアル酸の消失にシアリダーゼが関わっていることが初めて明らかになった。一方、Ra2に対し、神経保護的な作用をもつサイトカインで刺激を行うと、ポリシアル酸構造が逆に増加する傾向があることも明らかにした。これまで、ポリシアル酸の素早い変動に関わる知見は得られておらす、ポリシアル酸構造の制御メカニズムの解明が期待される。

  21. 鳥類の卵・精子相互作用を制御する糖タンパク質の同定と機能解析

    研究課題/研究課題番号:17380200  2005年 - 2007年

    松田 幹

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    担当区分:研究分担者 

    細胞間相互作用の視点から、配偶子間での特異的な認識と結合を制御すると予想される二種の糖たんぱく質(卵透明帯、zona pellucida、のZP糖タンパク質および精子表面のリン脂質結合タンパク質、MFG-E8)に関する構造と機能解析を進めた。ZP糖タンパク質については、リガンドブロット法により多様な組み合わせの中でZPB1とZPCが特異的に結合し、その会合に伴い分子間S-S結合を介したZPB1の二量体化が誘導され、それに伴う立体構造の変化により精子活性化能を獲得することを示唆した。またCOS7細胞で発現、分泌させたZPCは培養上清に添加された可溶性の産卵鶏血清ZPB1と会合して細胞表面にZPB1-ZPC複合体のマトリクスを形成することを明らかにした。さらに、可溶化して分離精製したZPCを可溶性ZPB1と反応させることにより卵透明帯マトリクスのin vitroでの再構築を試み、両ZP糖タンパク質は自己重合化して光学顕微鏡下で観察できる繊維状の複合体を形成することを発見した。一方、MFG-E8に関しては、精子表面以外にも細胞から分泌されるリン脂質膜小胞(エキソソーム)に局在し、乳腺上皮細胞のアポトーシスおよび脂肪細胞分化における細胞間認識での役割を示唆した。MFG-E8が膜小胞表面に存在して小胞と細胞との相互作用に重要な役割を持つことが明らかになったことから、ZP糖タンパク質マトリクスと膜小胞会合MFG-E8との複合超分子間の相互作用の解析への展開を進めている。

  22. 糖タンパク質のユニークなシアル酸重合体修飾の機能解析

    研究課題/研究課題番号:17046006  2005年 - 2006年

    佐藤 ちひろ

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    担当区分:研究代表者 

    配分額:4500000円 ( 直接経費:4500000円 )

    我々は、これまでの糖タンパク質上のシアル酸の存在状態に対する認識(モノ【tautomer】ポリ)を塗り替え、新たな概念(モノ【tautomer】オリゴ【tautomer】ポリ)を創出した。すなわちオリゴシアル酸の存在を仮定し、シアル酸重合体の微量検出方法を新たに開発し、その方法を用いてその存在証明を行った。本研究は糖タンパク質上のシアル酸重合体というユニークな糖鎖修飾が、どのような生物学的意義を持つのかを明らかにすることが目的である。本研究ではこれまで明らかになっていないシアル酸重合体の生物学的な意義の解明をT細胞、体液、ミクログリア細胞、生殖細胞を用いて試みた。T細胞では、糖タンパク質と糖脂質の共通糖鎖エピトープ構造である、ジシアル酸構造がラフトに存在し、T細胞の活性化に関わっていること、その際にST8Sia I, IV, VIの変動が起こっていることを明らかにした。また、体液においては、マウス血清中のplasminogen, vitronectin, IgLがジシアル酸構造修飾を受けていることを明らかにし、特にvitronectinのジシアル酸構造は肝切除後に減少するということが示した。また、脳においてはマウスミクログリア細胞にポリシアル酸構造が存在することを証明した。特にLPSで炎症性の刺激を行うと、ポリシアル酸構造は消失するが、IL4などの神経保護的な作用をもつサイトカインで刺激を行うと、ポリシアル酸構造が増加する傾向があることを明らかにした。特にLPS刺激によるポリシアル酸の消失はポリシアル酸合成に関わるST8SiaのmRNAの発現の減少だけでなく、シアリダーゼのmRNAの増加も同時におこっており、実際にシアリダーゼの活性の上昇が見られた。生殖細胞はウニ精子を用いた。このポリシアル酸構造は通常見られるα2,8結合ポリシアル酸構造ではなく、α2,9ポリシアル酸構造であった。この構造を持つflagellasialinを新規にクローニングし、同定を行った。製麻区表面上のα2,9ポリシアル酸構造はCaチャンネルを介した精子の鞭毛の運動性に関わっていることを明らかにした。

  23. 糖タンパク質のユニークなシアル酸重合体修飾の機能解析

    2005年

    科学研究費補助金  特定領域研究,課題番号:17046006

    佐藤 ちひろ

      詳細を見る

    担当区分:研究代表者 

  24. 糖タンパク質のユニークなシアル酸重合体修飾の機能解析

    2005年

    科学研究費助成事業  特定領域研究,課題番号:17046006

    佐藤 ちひろ

      詳細を見る

    担当区分:研究代表者  資金種別:競争的資金

  25. 神経細胞におけるシアル酸重合体の多様性と生物機能の解析

    研究課題/研究課題番号:16770073  2004年 - 2005年

    佐藤 ちひろ

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    担当区分:研究代表者 

    配分額:3300000円 ( 直接経費:3300000円 )

    シアル酸重合体とは、シアル酸同士が2〜数十残基結合した構造である。胎仔脳において、神経細胞やグリア細胞におけるNCAM上のポリシアル酸構造の研究はよく行われており、反接着分子として機能することにより、脳の発達に深く関わることが知られている。一方、脳内での免疫機構を司るマクロファージ様の細胞であるミクログリア上のシアル酸構造に関してこれまで解析が全くなされていなかった。我々はマウス新生児脳のプライマリーカルチャーおよびノミクログリア細胞株を用いて、ミクログリア細胞にジシアル酸構造だけでなくポリシアル酸が存在することを明らかにした。また、ミクログリア細胞はその活性化によって、神経組織に対し、trophicに働いたり、toxicに働くことが知られているが、その機構について詳しくはわかっていない。そこでミクログリアの機能におけるポリシアル酸構造の関わりを明らかにするために、まず、ミクログリア細胞株を用いて、活性化状態におけるポリシアル酸の変動を明らかにすることとした。LPSおよびIL4刺激という二つの異なる活性化状態におけるポリシアル酸構造の変動を、免疫染色および我々の開発したオリゴ・ポリシアル酸の化学的検出法により解析した。その結果、ミクログリア細胞のポリシアル酸はLPS刺激により速やかに消失すること、またIL-4刺激においてはそのポリシアル酸量が増加することが明らかになった。これまで、ポリシアル酸の消失は、脳の発達に伴う数週間から数ヶ月にわたる変動と考えられていたが、ミクログリアにおけるポリシアル酸の速やかな消失は、分単位という非常に素早い変化であった。このような素早い変動はポリシアル酸の研究のおいて初めての例である。また、この急激な消失はポリシアル酸がミクログリアの活性化に関わりがあることを示唆する。

  26. 神経細胞におけるシアル酸重合体の多様性と生物機能の解析

    2004年

    科学研究費補助金  若手研究(B),課題番号:16770073

    佐藤 ちひろ

      詳細を見る

    担当区分:研究代表者 

  27. 神経細胞におけるシアル酸重合体の多様性と生物機能の解析

    2004年

    科学研究費助成事業  若手研究(B),課題番号:16770073

    佐藤 ちひろ

      詳細を見る

    担当区分:研究代表者  資金種別:競争的資金

  28. 難消化性高分子量食品成分の消化管内動態と吸収機構

    研究課題/研究課題番号:14360073  2002年 - 2004年

    松田 幹

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    担当区分:研究分担者 

    卵アルブミン(OVA)は、未変性では難消化性であり卵アレルギーの主要アレルゲンとして知られている。このOVAをモデルタンパク質として、マウス消化管内から未消化のままで体内に吸収される現象について、腸管からの吸収と末梢血への移行について定性および定量的に解析した。経口投与後の末梢血中で検出されたOVAの生化学的性質をSDS-PAGEおよび等電点電気泳動法を用いて解析した。10mgをマウスの胃内に投与した後、30分後に、静脈より全先血し、血液を凝固させた後、血清を調製した。ウサギ抗OVA抗体をセファロースに固定化した固相抗体を用いて免疫沈降法により、マウス末梢血に含まれるOVAおよびその誘導体を沈降させ濃縮した。これをSDS-PAGEおよび免疫ブロット法により解析した結果、未分解のOVAと同じ位置に明確なバンドが検出され、また、分子量が僅かに小さい位置にも弱いバンドが検出された。しかし、消化管内容物中には検出された分子量1-3万のOVA分解断片はまったく検出されなかった。同様の結果は、ゲル濾過クロマトグラフィーによる血清中のOVAの分子量分布の解析からも得られた。この結果から、腸管内から体内へのOVA抗原の移行は、単純な拡散によるものではなく、未分解あるいは未変性の分子が優先的に取り込まれる未知の機構が存在する可能性が示唆された。また、等電点電気泳動により、OVAは同一分子量の3-5個のスポットとして検出されるが、末梢血中から回収されたOVAでは、塩基性側のスポットがより強く検出され、等電点がやや塩基性にシフトしていることが明らかとなった。このような生化学的変化は、OVAをマウス血清と反応させただけでは観察されなかった。これらの結果から、タンパク質が腸管内から吸収されて末梢血に移行する過程で、おそらく腸上皮を通過する過程で、何らかの修飾を受ける可能性が考えられる。

  29. 神経形成を制御する新規糖鎖オリゴシアル酸の作用機構の解明

    研究課題/研究課題番号:14780471  2002年 - 2003年

    佐藤 ちひろ

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    担当区分:研究代表者 

    配分額:2100000円 ( 直接経費:2100000円 )

    シアル酸は糖タンパク質や糖脂質を構成する酸性糖で、様々な生物学的現象において非常に重要な役割を担っている。通常、1残基が糖鎖の最外部に結合したモノシアル酸として存在するが、まれにその末端シアル酸残基の上にさらにシアル酸の直鎖ポリマーが結合するポリシアル酸構造として存在する。ポリシアル酸はその物理化学的性質により、細胞と細胞、細胞と細胞外基質の接着を阻害する方向に調節し、神経形成のモジュレーターとなっていることが明らかになってきた。一方、シアル酸の重合度が2から7のオリゴシアル酸構造の存在は糖タンパク質において、その存在はほとんど知られていなかった。我々は近年、オリゴシアル酸構造を微量で検出できる化学的方法、及び免疫化学的手法を世界で初めて開発し、それらの方法を用いて、哺乳動物の種々の臓器や組織において、オリゴシアル酸構造を持つ糖タンパク質が存在していること示した。本研究では、CD166がジシアル酸含有糖タンパク質であることを端緒に、T細胞上でも、神経細胞と同様にCD166がジシアロ糖タンパク質であり、活性化に関わることを示唆する知見を得た。またNeuro2A細胞で、ST8SiaVIが存在していることが明らかになった。さらにヒトミルク中にポリシアリル化をうけたCD36分子が存在し、発達段階特異的な発現変動をしていることを明らかにすると同時に、CD36はジシアリル化を受けていること、乳腺上皮細胞上に、ポリシアル酸とオリゴシアル酸を生合成する酵素の発現が、泌乳期特異的に変動することを明らかにした。さらに、HSP110ホモログであるウニ精子結合蛋白質がシアル酸結合レクチンであることが明らかになった。

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担当経験のある科目 (本学) 4

  1. 生物化学1

    2021

  2. バイオテクノロジー

    2020

  3. 糖鎖生物学特論

    2020

  4. 化学実験

    2020

担当経験のある科目 (本学以外) 9

  1. 分子細胞機能学輪講I

    名古屋大学)

  2. 分子細胞機能学基盤実験

    名古屋大学)

  3. 生物化学1

    名古屋大学)

  4. 情報リテラシー入門

    名古屋大学)

  5. 応用生命科学実験実習II

    名古屋大学)

  6. 応用生命科学実験実習I

    名古屋大学)

  7. 分子細胞機能学特論I

    名古屋大学)

  8. 分子細胞機能学演習I

    名古屋大学)

  9. 分子細胞機能学基礎講義

    名古屋大学)

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