Updated on 2024/10/01

写真a

 
NAKAJIMA Chikako
 
Organization
Graduate School of Science Assistant Professor
Graduate School
Graduate School of Science
Undergraduate School
School of Science Department of Biological Science
Title
Assistant Professor

Degree 3

  1. Dr. rer. nat （ 2011.12   University of Freiburg ） 

  2. MSc （ 2006.3   Tokyo Institute of Technology ） 

  3. BSc （ 2004.3   Tokyo University of Science ） 

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Research Interests 7

  1. Neurogenesis

  2. Injured brain

  3. Biomaterial

  4. Neuronal regeneration

  5. Migrating neurons

  6. Transcription factor

  7. Ventricular-subventricular zone

To the head of Research Interests.▲

Research Areas 1

  1. Life Science / Neuroscience-general  / Neuroscience

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Research History 6

  1. Nagoya University   Assistant Professor

    2024.9

  2. Nagoya City University   Graduate School of Medical Sciences Department of Developmental and Regenerative Biology

    2024

  3. Nagoya City University   Graduate School of Medical Sciences, Department of Developmental and Regenerative Biology   Designated assistant professor

    2019 - 2024

  4. Perseus Proteomics Inc.   R&D

    2019

  5. University of Mainz   Dept. Physiological chemistry (Berninger lab)

    2014 - 2018

    　 More details

    Country：Germany

  6. Albert-Ludwigs-Universität Freiburg (University of Freiburg)   Neuroanatomy II (May lab)

    2012 - 2013

    　 More details

    Country：Germany

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Education 4

  1. Albert-Ludwigs-Universität Freiburg (University of Freiburg)   Department of Medicine   Neuroanatomy II

    2007.3 - 2011.12

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    Country： Germany

  2. Tokyo Institute of Technology   Interdisciplinary Graduate School of Science and Engineering   Environmental Chemistry and Engineering, Chemical Resources Laboratory

    2006.4 - 2007.3

  3. Tokyo Institute of Technology

    2004.4 - 2006.3

    　 More details

    Country： Japan

  4. Tokyo University of Science

    2000.4 - 2004.3

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    Country： Japan

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Professional Memberships 5

  1. The Japanese Society for Regenerative Medicine

    2023

  2. The Japanese Society for Neurochemistry

    2021

  3. The Japan Neuroscience Society

    2020

  4. Society for Neuroscience

    2009

  5. The German Neuroscience Society

    2009

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Committee Memberships 1

  1. 成体脳のニューロン新生懇談会   広報委員  

    2022.10   

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Awards 3

  1. Bioindustry Research Award 2024

    2024.7   Japan Bioindustry Association  

  2. Travel Grant

    2014.10   Bavaria California Technology Center (BaCaTec)  

  3. FTN Postdoctoral Fellowship

    2014.3   Focus Program Translational Neurosciences (FTN)  

To the head of Awards.▲
 

Papers 7

  1. Identification of the growth cone as a probe and driver of neuronal migration in the injured brain Reviewed

    Chikako Nakajima, Masato Sawada, Eri Umeda, Yuma Takagi, Nakashima, N., Kuboyama, K., Kaneko, N., Yamamoto, S., Nakamura, H., Shimada, N., Nakamura, K., Matsuno, K., Uesugi, S., Vep?ek, N.A., K{\"u}llmer, F., Nasufovi?, V., Uchiyama, H., Nakada, M., Otsuka, Y., Ito, Y., Herranz-P{\'e}rez, V., Garc{\'i}a-Verdugo, J.M., Ohno, N., Arndt, H.-D., Trauner, D., Tabata, Y., Igarashi, M., Kazunibu Sawamoto

    Nature Communications   Vol. 15 ( 1 ) page： 1877   2024.3

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    Authorship：Lead author   Publishing type：Research paper (scientific journal)  

    DOI： 10.1038/s41467-024-45825-8

    Scopus

  2. Amphiphilic peptide-tagged N-cadherin forms radial glial-like fibers that enhance neuronal migration in injured brain and promote sensorimotor recovery Reviewed

    Yuya Ohno*, Chikako Nakajima* (equal first authorship), Itsuki Ajioka, Takahiro Muraoka, Atsuya Yaguchi, Teppei Fujioka, Saori Akimoto, Misaki Matsuo, Ahmed Lotfy, Sayuri Nakamura, Vicente Herranz-Pérez, José Manuel García-Verdugo, Noriyuki Matsukawa, Naoko Kaneko, Kazunobu Sawamoto

    Biomaterials   Vol. 294   page： 122003   2023.3

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    Authorship：Lead author   Publishing type：Research paper (scientific journal)   Publisher：Elsevier BV  

    DOI： 10.1016/j.biomaterials.2023.122003

    Scopus

  3. Postnatal neuronal migration in health and disease Reviewed

    Chikako Nakajima, Masato Sawada, Kazunobu Sawamoto

    Current Opinion in Neurobiology   Vol. 66   page： 1 - 9   2021.2

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    Authorship：Lead author   Publishing type：Research paper (scientific journal)   Publisher：Elsevier BV  

    DOI： 10.1016/j.conb.2020.06.001

    Scopus

    PubMed

  4. The lipoprotein receptor LRP1 modulates sphingosine-1-phosphate signaling and is essential for vascular development Reviewed

    Chikako Nakajima, Philipp Haffner, Sebastian M. Goerke, Kai Zurhove, Giselind Adelmann, Michael Frotscher, Joachim Herz, Hans H. Bock, Petra May

    Development   Vol. 141 ( 23 ) page： 4513 - 4525   2014.12

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    Authorship：Lead author   Language：English   Publishing type：Research paper (scientific journal)   Publisher：COMPANY OF BIOLOGISTS LTD  

    Low density lipoprotein receptor-related protein 1 (LRP1) is indispensable for embryonic development. Comparing different genetically engineered mouse models, we found that expression of Lrp1 is essential in the embryo proper. Loss of LRP1 leads to lethal vascular defects with lack of proper investment with mural cells of both large and small vessels. We further demonstrate that LRP1 modulates Gi-dependent sphingosine-1-phosphate (S1P) signaling and integrates S1P and PDGF-BB signaling pathways, which are both crucial for mural cell recruitment, via its intracellular domain. Loss of LRP1 leads to a lack of S1P-dependent inhibition of RAC1 and loss of constraint of PDGF-BB-induced cell migration. Our studies thus identify LRP1 as a novel player in angiogenesis and in the recruitment and maintenance of mural cells. Moreover, they reveal an unexpected link between lipoprotein receptor and sphingolipid signaling that, in addition to angiogenesis during embryonic development, is of potential importance for other targets of these pathways, such as tumor angiogenesis and inflammatory processes.

    DOI： 10.1242/dev.109124

    Web of Science

    PubMed

  5. Low Density Lipoprotein Receptor-related Protein 1 (LRP1) Modulates N-Methyl-D-aspartate (NMDA) Receptor-dependent Intracellular Signaling and NMDA-induced Regulation of Postsynaptic Protein Complexes Reviewed

    Chikako Nakajima, Akos Kulik, Michael Frotscher, Joachim Herz, Michael Schaefer, Hans H. Bock, Petra May

    Journal of Biological Chemistry   Vol. 288 ( 30 ) page： 21909 - 21923   2013.7

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    Authorship：Lead author   Language：English   Publishing type：Research paper (scientific journal)   Publisher：AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC  

    The lipoprotein receptor LRP1 is essential in neurons of the central nervous system, as was revealed by the analysis of conditional Lrp1-deficient mouse models. The molecular basis of its neuronal functions, however, is still incompletely understood. Here we show by immunocytochemistry, electron microscopy, and postsynaptic density preparation that LRP1 is located postsynaptically. Basal and NMDA-induced phosphorylation of the transcription factor cAMP-response element-binding protein (CREB) as well as NMDA target gene transcription are reduced in LRP1-deficient neurons. In control neurons, NMDA promotes -secretase-dependent release of the LRP1 intracellular domain (LRP1-ICD). However, pull-down and chromatin immunoprecipitation (ChIP) assays showed no direct interaction between the LRP1-ICD and either CREB or target gene promoters. On the other hand, NMDA-induced degradation of the postsynaptic scaffold protein PSD-95 was impaired in the absence of LRP1, whereas its ubiquitination was increased, indicating that LRP1 influences the composition of postsynaptic protein complexes. Accordingly, NMDA-induced internalization of the AMPA receptor subunit GluA1 was impaired in LRP1-deficient neurons. These results show a role of LRP1 in the regulation and turnover of synaptic proteins, which may contribute to the reduced dendritic branching and to the neurological phenotype observed in the absence of LRP1.

    DOI： 10.1074/jbc.M112.444364

    Web of Science

    PubMed

  6. Quantitative Regional and Ultrastructural Localization of the Ca(v)2.3 Subunit of R-type Calcium Channel in Mouse Brain Reviewed

    Laxmi Kumar Parajuli, Chikako Nakajima, Akos Kulik, Ko Matsui, Toni Schneider, Ryuichi Shigemoto, Yugo Fukazawa

    Journal of Neuroscience   Vol. 32 ( 39 ) page： 13555 - 13567   2012.9

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    Language：English   Publishing type：Research paper (scientific journal)   Publisher：SOC NEUROSCIENCE  

    R-type calcium channels (RTCCs) are well known for their role in synaptic plasticity, but little is known about their subcellular distribution across various neuronal compartments. Using subtype-specific antibodies, we characterized the regional and subcellular localization of Ca(v)2.3 in mice and rats at both light and electron microscopic levels. Ca(v)2.3 immunogold particles were found to be predominantly presynaptic in the interpeduncular nucleus, but postsynaptic in other brain regions. Serial section analysis of electron microscopic images from the hippocampal CA1 revealed a higher density of immunogold particles in the dendritic shaft plasma membrane compared with the pyramidal cell somata. However, the labeling densities were not significantly different among the apical, oblique, or basal dendrites. Immunogold particles were also observed over the plasma membrane of dendritic spines, including both synaptic and extra-synaptic sites. Individual spine heads contained <20 immunogold particles, with an average density of similar to 260 immunoparticles per mu m(3) spine head volume, in accordance with the density of RTCCs estimated using calcium imaging (Sabatini and Svoboda, 2000). The Ca(v)2.3 density was variable among similar-sized spine heads and did not correlate with the density in the parent dendrite, implying that spines are individual calcium compartments operating autonomously from their parent dendrites.

    DOI： 10.1523/JNEUROSCI.1142-12.2012

    Web of Science

    PubMed

  7. Gamma-Secretase Limits the Inflammatory Response Through the Processing of LRP1 Reviewed

    Kai Zurhove, Chikako Nakajima, Joachim Herz, Hans H. Bock, Petra May

    Science Signaling   Vol. 1 ( 47 ) page： ra15   2008.11

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    Language：English   Publishing type：Research paper (scientific journal)   Publisher：AMER ASSOC ADVANCEMENT SCIENCE  

    Inflammation is a potentially self-destructive process that needs tight control. We have identified a nuclear signaling mechanism through which the low-density lipoprotein receptor-related protein 1 (LRP1) limits transcription of lipopolysaccharide (LPS)-inducible genes. LPS increases the proteolytic processing of the ectodomain of LRP1, which results in the gamma-secretase-dependent release of the LRP1 intracellular domain (ICD) from the plasma membrane and its translocation to the nucleus, where it binds to and represses the interferon-gamma promoter. Basal transcription of LPS target genes and LPS-induced secretion of proinflammatory cytokines are increased in the absence of LRP1. The interaction between LRP1-ICD and interferon regulatory factor 3 (IRF-3) promotes the nuclear export and proteasomal degradation of IRF-3. Feedback inhibition of the inflammatory response through intramembranous processing of LRP1 thus defines a physiological role for gamma-secretase.

    DOI： 10.1126/scisignal.1164263

    Web of Science

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To the head of Papers.▲

MISC 3

  1. 移動する神経細胞のアクセル・ブレーキを司る構造を発見 Invited

    中嶋智佳子, 澤本和延

    名古屋市立大学大学院医学研究科・医学部発行広報誌 『瑞医 ～世界に羽ばたくMEDIPORT～』   ( 53 ) page： 4   2024.6

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    Authorship：Lead author   Publishing type：Article, review, commentary, editorial, etc. (bulletin of university, research institution)  

  2. Single cell level analyses for studying the mechanisms for neuronal migration and regeneration Invited

    中嶋智佳子, 澤本和延

    月刊Precision Medicine   Vol. 4 ( 8 ) page： 60 - 63   2021.8

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    Authorship：Lead author  

    J-GLOBAL

  3. Deciphering the mechanisms of postnatal neuronal migration by the advanced methods in morphological and single cell RNA-seq analysis Invited

    中嶋智佳子, 澤本和延

    月刊細胞   Vol. 52 ( 13 ) page： 52 (774) - 54 (776)   2020.11

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    Authorship：Lead author  

    J-GLOBAL

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Presentations 15

  1. Identification of growth cones of newborn neurons, a primary regulator of neuronal migration in the injured brain

    Chikako Nakajima, Masato Sawada, Norihiko Nakashima, Kazuya Kuboyama, Naoko Kaneko, Naoki Shimada, Koichiro Nakamura, Kumiko Matsuno, Shoji Uesugi, Hiromitsu Uchiyama, Yasuyuki Ito, Nobuhiko Ohno, Yasuhiko Tabata, Michihiro Igarashi, Kazunobu Sawamoto

    2024.7.26 

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    Event date： 2024.7

    Language：English   Presentation type：Oral presentation (general)  

  2. The growth cone of migrating neurons as a primary sensor and migratory actuator in the injured brain environment

    C. Nakajima, M. Sawada, E. Umeda, Y. Takagi, N. Nakashima, K. Kuboyama, N. Kaneko, S. Yamamoto, H. Nakamura, N. Shimada, K. Nakamura, K. Matsuno, S. Uesugi, N.A Vepřek, F. Küllmer, V. Nasufović, H. Uchiyama, M. Nakada, Y. Otsuka, Y. Ito, V. Herranz-Pérez, J.M. García-Verdugo, N. Ohno, H.-D. Arnd, D. Trauner, Y. Tabata, M. Igarashi, K. Sawamoto

    FENS Forum 2024  2024.6.28 

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    Event date： 2024.6

    Language：English   Presentation type：Poster presentation  

  3. 傷害脳内のニューロン移動を制御する成長円錐の同定

    中嶋 智佳子, 澤田 雅人, 梅田 恵里花, 高木 佑真, 中島 徳彦, 久保山 和哉, 金子 奈穂子, 山本 悟暁, 中村 春野, 島田 直樹, 中村 耕一郎, 松野 久美子, 上杉 昭二, Nynke A. Vepřek, Florian Küllmer, Veselin Nasufovi, 内山 博允, 中田 克, 大塚 祐二, 伊藤 泰行, Vicente Herranz-Pérez, José Manuel García-Verdugo, 大野 伸彦, Hans-Dieter Arnd, Dirk Trauner, 田畑 泰彦, 五十嵐 道弘, 澤本 和延

    第17回神経発生討論会・第20回成体脳のニューロン新生懇談会合同大会  2024.3.9 

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    Event date： 2024.3

    Presentation type：Oral presentation (general)  

  4. Promotion of neuronal migration to the site of brain injury facilitates functional recovery Invited

    Chikako NAKAJIMA, Yuya OHNO, Masato SAWADA, Naoko KANEKO, Kazunobu SAWAMOTO

    The Joint Meeting of The 64th Annual Meeting of the Japanese Society of Neuropathology and the 66th Annual Meeting of the Japanese Society for Neurochemistry  2023.7.8 

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    Event date： 2023.7

    Presentation type：Oral presentation (invited, special)  

  5. Functions of lincRNAs in physiological and induced reprogramming of astrocytes-to-neurons

    Chikako Nakajima, Sudhir Thakurela, Vijay K Tiwari, Benedikt Berninger

    22nd Biennial Meeting of the International Society of Developmental Neuroscience (ISDN)  2018.5.23 

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    Event date： 2018.5

    Presentation type：Poster presentation  

  6. 新生ニューロンの移動促進による神経再生

    中嶋智佳子

    名古屋大学 生命理学セミナー  2024.6.18 

  7. 成長円錐の同定による傷害脳での新たなニューロン移動機構の解明

    中嶋 智佳子, 澤田 雅人, 梅田 恵里花, 高木 佑真, 中島 徳彦, 久保山 和哉, 金子 奈穂子, 山本 悟暁, 中村 春野, 島田 直樹, 中村 耕一郎, 松野 久美子, 上杉 昭二, Nynke A. Vepřek, Florian Küllmer, Veselin Nasufovi, 内山 博允, 中田 克, 大塚 祐二, 伊藤 泰行, Vicente Herranz-Pérez, José Manuel García-Verdugo, 大野 伸彦, Hans-Dieter Arnd, Dirk Trauner, 田畑 泰彦, 五十嵐 道弘, 澤本 和延

    第74回脳の医学・生物学研究会 第3回日本神経化学会若手KYOEN 合同大会  2024.5.18 

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    Presentation type：Oral presentation (general)  

  8. The function of long intergenic ncRNA in forced neurogenesis and brain development Invited

    Chikako Nakajima, Sudhir Thakurela, Vijay K Tiwari, Benedikt Berninger

    The Belgian Society for Cell and Developmental Biology (BSCDB)  2015.6.5 

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    Presentation type：Oral presentation (general)  

  9. Molecular interactions between migratory neurons and their scaffold cells in the injured brain

    Kazuya Kuboyama, Rasmus Rydbirk, Chikako Nakajima, Mami Matsumoto, Masato Sawada, Koya Kawase, Nobuhiko Ohno, Konstantin Khodosevich, Kazunobu Sawamoto

    2024.7.25 

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    Event date： 2024.7

    Presentation type：Poster presentation  

  10. The charachterization of long intervening ncRNA in forced neurogenesis and brain development

    Chikako Nakajima, Sudhir Thakurela, Vijay K Tiwari, Benedikt Berninger

    Abcam meeting: Programming and reprogramming the brain  2017.4.3 

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    Event date： 2017.4

    Presentation type：Poster presentation  

  11. 成体脳を移動する新生ニューロンにおける成長円錐の形態と動態

    高木佑真, 澤田雅人, 中嶋智佳子, 松本真実, 大野伸彦, 五十嵐道弘, 澤本和延

    第63回日本神経化学会  2020.9.10 

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    Presentation type：Poster presentation  

  12. 傷害脳への足場バイオマテリアルの導入による新生ニューロンの移動促進および脳機能回復

    中嶋智佳子, 大野雄也, 澤田雅人, 金子奈緒子, 澤本和延

    第46回日本神経科学大会  2023.8.3 

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    Presentation type：Poster presentation  

  13. 移動ニューロンと足場細胞間における接着/脱接着の分子メカニズム

    久保山 和哉, Rasmus Rydbirk, 中嶋 智佳子, 古田 美穂, 松本 真実, 澤田 雅人, 川瀬 恒哉, 宮本 拓哉, 榊原悠紀菜, 川村 直矢, 鈴木 崇宏, 大野 信彦, Konstantin Khodosevich, 澤本 和延

    第74回脳の医学・生物学研究会 第3回日本神経化学会若手KYOUEN合同大会  2024.5.18 

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    Presentation type：Oral presentation (general)  

  14. 細胞外マトリックスを含有する人工足場を用いた傷害脳組織における新生ニューロンの移動促進

    長瀬次郎, 中嶋智佳子, 中村小百合, 澤田雅人, 澤本和延

    第64回日本神経化学会  2021.9.30 

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    Presentation type：Poster presentation  

  15. 細胞外マトリックスによる傷害大脳皮質における新生ニューロンの移動促進

    山本悟暁, 中嶋智佳子, 中村春野, 島田直樹, 中村耕一郎, 上杉昭二, 田畑泰彦, 澤本和延

    NEURO2022（第45回日本神経科学大会、第65回日本神経化学会、第32回日本神経回路学会合同大会）  2022.7.2 

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    Presentation type：Poster presentation  

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KAKENHI (Grants-in-Aid for Scientific Research) 3

  1. Aging associated changes in neurogenesis and neuronal migration in postnatal common marmosets

    Grant number：23K19406  2023.8 - 2025.3

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Research Activity Start-up

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    Authorship：Principal investigator 

    Grant amount：\2860000 （ Direct Cost: \2200000 、 Indirect Cost：\660000 ）

  2. Functions of intergenic long non-coding RNA in physiological and forced neurogenesis

    2015.10 - 2017.9

    マインツ大学  Intramural research funding (Forschungsförderung StufeI) 

    Chikako Nakajima

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    Authorship：Principal investigator 

  3. Long non-coding RNAs in physiological neurogenesis and induced neurogenesis

    2014.3 - 2017.7

    FTN Scholorship Program  Postdoctoral fellowship 

    Chikako Nakajima

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    Authorship：Principal investigator 

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Industrial property rights 3

  1. ニューロンの移動促進剤およびその利用

    澤本和延, 金子奈穂子, 中嶋智佳子, 大野雄也, 味岡逸樹, 村岡貴博

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    Applicant：公立大学法人名古屋市立大学

    Application no：特願PCT/JP2023/8130  Date applied：2023.3

  2. ニューロンの移動促進剤およびその利用

    澤本和延, 金子奈穂子, 中嶋智佳子, 大野雄也, 味岡逸樹, 村岡貴博

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    Applicant：公立大学法人名古屋市立大学

    Application no：特願2022-34331  Date applied：2022.3

  3. 脳疾患治療剤及びその利用

    澤本和延, 澤田雅人, 五十嵐道弘, 中嶋智佳子

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    Applicant：公立大学法人名古屋市立大学

    Application no：特願PCT/JP2020/47678  Date applied：2020.12

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Teaching Experience (Off-campus) 7

  1. Brain Science

    2024 （Nagoya City University）

  2. Brain science and society, Active learning

    2023 - 2024 （Nagoya City University）

  3. -

    2020 - 2024 （Nagoya City University）

  4. ー

    2019 - 2024 （Nagoya City University）

  5. -

    2011.10 - 2012.3 （Albert-Ludwigs-Universität Freiburg (University of Freiburg)）

  6. 医学部 選択実習実験コース

    2009.10 - 2010.3 （フライブルク大学）

  7. 医学部 分子生物学実習

    2008.4 - 2008.9 （フライブルク大学）

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Social Contribution 2

  1. 名古屋市立大学 大学丸ごと研究室体験

    Role(s)：Demonstrator

    2022

  2. NPO団体 Science Innovation Union 産学連携セミナー企画・開催

    Role(s)：Planner,　Organizing member

    2018

To the head of Social Contribution.▲

Media Coverage 8

  1. Deciphering the tip of migrating neurons: Discovery of growth cone in migrating neurons involved in promoting neuronal migration and regeneration in the brain after injury Internet

    EurekAlert!  2024.3

  2. 神経細胞の先端に司令塔機能 名古屋市大など発見、歩行機能回復など期待 Newspaper, magazine

    日刊工業新聞  2024.3

  3. 損傷した脳の神経再生、名古屋市立大グループが成功 マウスの歩行機能回復 Newspaper, magazine

    中日新聞  2024.3

  4. ニッケのゼラチン不織布「ジェノセル」 ニューロンに関する名古屋市立大大学院の研究に貢献 Newspaper, magazine

    繊研新聞社  2024.3

  5. Discovery of Growth Cone Boosts Brain Injury Recovery Internet

    The Mirage  2024.3

  6. 脳傷害後の神経再生を促す 超分子バイオマテリアルの開発に成功 Internet

    生理学研究所プレスリリース  2023.3

  7. 生理学研究所・名古屋市立大・同志社大など、脳傷害後の神経再生を促す超分子バイオマテリアルの開発に成功 Newspaper, magazine

    日本経済新聞  2023.2

  8. 脳傷害後の神経再生を促す超分子バイオマテリアルの開発に成功 Internet

    時事メディカル  2023.2

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Academic Activities 2

  1. 成体脳のニューロン新生懇談会 運営委員 広報担当

    Role(s)：Planning, management, etc.

    2022

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    Type：Academic society, research group, etc. 

  2. FTN Fellows Symposium 2015

    Role(s)：Planning, management, etc.

    2015.10

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    Type：Competition, symposium, etc. 

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