研究者詳細 - 加藤　竜司

論文 - 加藤　竜司

分割表示 112 件中 1 - 20 件目／全件表示 >>

Importance of dataset design in developing robust U-Net models for label-free cell morphology evaluation.

Shiina T, Kimura K, Takemoto Y, Tanaka K, Kato R

Journal of bioscience and bioengineering 139 巻 ( 4 ) 頁： 329 - 339 2025年4月

記述言語：英語出版者・発行元：Journal of Bioscience and Bioengineering

Advances in regenerative medicine highlighted the need for label-free cell image analysis to replace conventional microscopic observation for non-invasive cell quality evaluation. Image-based evaluation provides an efficient, quantitative, and automated approach to cell analysis, but segmentation remains a critical and challenging step. In this study, we investigated how training dataset design influenced the robustness of U-Net models for cell segmentation, focusing on challenges posed by limited data availability in cell culture. Using 2592 image pairs from four cell types representing key morphological categories, we constructed 42 investigation patterns to evaluate the effects of dataset size, dataset content, and morphological diversity on model performance. Our results showed that robust segmentation models could be developed with approximately 10 raw images captured using a 4× objective lens, a much smaller dataset than typically assumed. The dataset content was found to be crucial: training dataset images that captured commonly observed cell patterns yielded more robust models compared to those capturing rare or irregular cell patterns, which often impaired model performance with large deviations. Additionally, including both spindle and round cell morphologies in the training datasets improved model robustness when tested across all four cell types, while datasets restricted to a single morphology type could not achieve robust models. These findings highlight the importance of curating datasets that capture representative yet diverse cell morphologies. By addressing critical questions about dataset design, this study provides actionable guidance for the effective use of deep learning-based cell segmentation models in manufacturing and research applications.

DOI： 10.1016/j.jbiosc.2025.01.004

Scopus

PubMed

Medicinal cannabis extracts are neuroprotective against Aβ<sub>1-42</sub>-mediated toxicity in vitro Open Access

Marsh, DT; Shibuta, M; Kato, R; Smid, SD

BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY 135 巻 ( 5 ) 頁： 575 - 592 2024年11月

記述言語：英語出版者・発行元：Basic and Clinical Pharmacology and Toxicology

Background: Phytocannabinoids inhibit the aggregation and neurotoxicity of the neurotoxic Alzheimer's disease protein β amyloid (Aβ). We characterised the capacity of five proprietary medical cannabis extracts, heated and non-heated, with varying ratios of cannabidiol and Δ9-tetrahydrocannabinol and their parent carboxylated compounds to protect against lipid peroxidation and Aβ-evoked neurotoxicity in PC12 cells. Methods: Neuroprotection against lipid peroxidation and Aβ1–42-induced cytotoxicity was assessed using the thiazolyl blue tetrazolium bromide (MTT) assay. Transmission electron microscopy was used to visualise phytocannabinoid effects on Aβ1–42 aggregation and fluorescence microscopy. Results: Tetrahydrocannabinol (THC)/tetrahydrocannabinolic acid (THCA)-predominant cannabis extracts demonstrated the most significant overall neuroprotection against Aβ1–42-induced loss of PC12 cell viability. These protective effects were still significant after heating of extracts, while none of the extracts provided significant neuroprotection to lipid peroxidation via tbhp exposure. Modest inhibition of Aβ1–42 aggregation was demonstrated only with the non-heated BC-401 cannabis extract, but overall, there was no clear correlation between effects on fibrils and conferral of neuroprotection. Conclusions: These findings highlight the variable neuroprotective activity of cannabis extracts containing major phytocannabinoids THC/THCA and cannabidiol (CBD)/cannabidiolic acid (CBDA) on Aβ-evoked neurotoxicity and inhibition of amyloid β aggregation. This may inform the future use of medicinal cannabis formulations in the treatment of Alzheimer's disease and dementia.

DOI： 10.1111/bcpt.14078

Editorial: Artificial intelligence in predicting, determining and controlling cell phenotype or tissue function in inflammatory diseases Open Access

Hart, ML; Kato, R; Rolauffs, B

FRONTIERS IN IMMUNOLOGY 15 巻頁： 1443534 2024年6月

Construction of transcript regulation mechanism prediction models based on binding motif environment of transcription factor AoXlnR in <i>Aspergillus oryzae</i>

Oka, H; Kojima, T; Kato, R; Ihara, K; Nakano, H

JOURNAL OF BIOINFORMATICS AND COMPUTATIONAL BIOLOGY 22 巻 ( 03 ) 頁： 2450017 2024年6月

記述言語：英語出版者・発行元：Journal of Bioinformatics and Computational Biology

DNA-binding transcription factors (TFs) play a central role in transcriptional regulation mechanisms, mainly through their specific binding to target sites on the genome and regulation of the expression of downstream genes. Therefore, a comprehensive analysis of the function of these TFs will lead to the understanding of various biological mechanisms. However, the functions of TFs in vivo are diverse and complicated, and the identified binding sites on the genome are not necessarily involved in the regulation of downstream gene expression. In this study, we investigated whether DNA structural information around the binding site of TFs can be used to predict the involvement of the binding site in the regulation of the expression of genes located downstream of the binding site. Specifically, we calculated the structural parameters based on the DNA shape around the DNA binding motif located upstream of the gene whose expression is directly regulated by one TF AoXlnR from Aspergillus oryzae, and showed that the presence or absence of expression regulation can be predicted from the sequence information with high accuracy (AUPRC=0.8-1.0) by machine learning incorporating these parameters.

DOI： 10.1142/S0219720024500173

Web of Science

Scopus

PubMed

Image-based hybrid model incorporating initial spatial distribution for mesenchymal stem cell cultivation process design

Hirono, K; Hayashi, Y; Udugama, IA; Takemoto, Y; Kato, R; Kino-oka, M; Sugiyama, H

AICHE JOURNAL 2024年4月

出版者・発行元：AIChE Journal

This work presents an image-based hybrid model incorporating the initial spatial distribution for mesenchymal stem cell (MSC) cultivation process design. First, three levels of seeding bias in static MSC cultivation were experimentally investigated, and the resulting initial distribution was quantified using phase contrast microscopy image analysis. Second, the observed spatial heterogeneity was defined as a new parameter by calculating the standard deviation of the seeded cell number fraction among numerical 8 × 8 tiles on two-dimensional plates. Third, the parameter was incorporated into kinetic models to consider spatial growth limitation. The model was then applied to simulate MSC cultivation processes with experimental data. Using dynamic and stochastic simulation outputs, feasible ranges of cell-harvesting time could be determined to satisfy a given requirement for the minimum cell number and acceptable confluency level. The developed hybrid model could serve as a basis for quantitative decision-making in the design of MSC cultivation processes.

DOI： 10.1002/aic.18452

Web of Science

Scopus

Prediction of antibody production performance change in Chinese hamster ovary cells using morphological profiling. 査読有り

Hisada T, Imai Y, Takemoto Y, Kanie K, Kato R

Journal of bioscience and bioengineering 2024年3月

Development of novel waxy bone haemostatic agents composed of biodegradable polymers with osteogenic-enhancing peptides in rabbit models 査読有り

Ohno, T; Suenaga, H; Yamawaki-Ogata, A; Kanie, K; Kato, R; Uto, K; Ebara, M; Ito, H; Narita, Y; Usui, A; Mutsuga, M

Interdisciplinary cardiovascular and thoracic surgery 37 巻 ( 5 ) 2023年11月

The structurally diverse phytocannabinoids cannabichromene, cannabigerol and cannabinol significantly inhibit amyloid β-evoked neurotoxicity and changes in cell morphology in PC12 cells. 査読有り国際共著

Marsh DT, Sugiyama A, Imai Y, Kato R, Smid SD

Basic & clinical pharmacology & toxicology 2023年9月

Automated cell isolation from photodegradable hydrogel based on fluorescence image analysis. 査読有り

Shinji Sugiura, Shinya Yamahira, Masato Tamura, Kazumi Shin, Mayu Shibuta, Taku Satoh, Yui Matsuzawa, Gen Fujii, Fumiki Yanagawa, Michihiro Mutoh, Masumi Yanagisawa, Ryuji Kato, Hirofumi Matsui

BIOTECHNOLOGY AND BIOENGINEERING 2023年3月

Novel functional peptide for next-generation vital pulp therapy 査読有り

Watanabe Masakatsu, Okamoto Motoki, Komichi Shun, Huang Hailing, Matsumoto Sayoko, Moriyama Kiichi, Ohshima Jun, Abe Shotaro, Morita Masayoshi, Ali Manahil,, Takebe Katsuki, Kozaki Ikko, Fujimoto Akiyo, Kanie Kei, Kato Ryuji, Uto Kenichiro, Ebara Mitsuhiro, Yamawaki-Ogata Aika, Narita Yuji, Takahashi Yusuke, Hayashi Mikako

JOURNAL OF DENTAL RESEARCH 102 巻 ( 3 ) 頁： 322 - 330 2023年3月

Bioinformatics in bioscience and bioengineering: Recent advances, applications, and perspectives 査読有り

Uesaka Kazuma, Oka Hiroya, Kato Ryuji, Kanie Kei, Kojima Takaaki, Tsugawa Hiroshi, Toda Yosuke, Horinouchi Takaaki

JOURNAL OF BIOSCIENCE AND BIOENGINEERING 134 巻 ( 5 ) 頁： 363 - 373 2022年11月

天野日出, 木村和恵, 今井佑太, 加藤竜司, 中澤温子, 城田千代栄, 滝本愛太朗, 住田亙, 牧田智, 岡本眞宗, 安井昭洋, 高田瞬也, 中川洋一, 加藤大幾, 檜顕成, 内田広夫

小児外科 54 巻 ( 10 ) 頁： 1007 - 1011 2022年10月

Morphology-based noninvasive early prediction of serial-passage potency enhances the selection of clone-derived high-potency cell bank from mesenchymal stem cells 査読有り

Suyama Takashi, Takemoto Yuto, Miyauchi Hiromi, Kato Yuko, Matsuzaki Yumi, Kato Ryuji

INFLAMMATION AND REGENERATION 42 巻 ( 1 ) 頁： 30 2022年10月

Label-free morphological sub-population cytometry for sensitive phenotypic screening of heterogenous neural disease model cells 査読有り

Imai Yuta, Iida Madoka, Kanie Kei, Katsuno Masahisa, Kato Ryuji

SCIENTIFIC REPORTS 12 巻 ( 1 ) 頁： 9296 2022年6月

Bi-layered carboxymethyl cellulose-collagen vitrigel dual-surface adhesion-prevention membrane 査読有り

Wang Yue, Kanie Kei, Takezawa Toshiaki, Horikawa Miki, Kaneko Kyoshiro, Sugimoto Ayako, Yamawaki-Ogata Aika, Narita Yuji, Kato Ryuji

CARBOHYDRATE POLYMERS 285 巻頁： 119223 2022年6月

Myc supports self-renewal of basal cells in the esophageal epithelium. 査読有り国際共著

Tomoaki Hishida, Eric Vazquez-Ferrer, Yuriko Hishida-Nozaki, Yuto Takemoto, Fumiyuki Hatanaka, Kei Yoshida, Javier Prieto, Sanjeeb Kumar Sahu, Yuta Takahashi, Pradeep Reddy, David D O'Keefe, Concepcion Rodriguez Esteban, Paul S Knoepfler, Estrella Nuñez Delicado, Antoni Castells, Josep M Campistol, Ryuji Kato, Hiroshi Nakagawa, Juan Carlos Izpisua Belmonte

FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY 10 巻頁： 786031 2022年3月

Collection of Data Variation Using a High-Throughput Image-Based Assay Platform Facilitates Data-Driven Understanding of TRPA1 Agonist Diversity 査読有り

Terada Yuko, Tanaka Kenjiro, Matsuyama Minami, Fujitani Masaya, Shibuya Masatoshi, Yamamoto Yoshihiko, Kato Ryuji, Ito Keisuke

APPLIED SCIENCES 12 巻 ( 3 ) 2022年2月

Morphological heterogeneity description enabled early and parallel non-invasive prediction of T-cell proliferation inhibitory potency and growth rate for facilitating donor selection of human mesenchymal stem cells 査読有り

Imai Yuta, Kanie Kei, Kato Ryuji

INFLAMMATION AND REGENERATION 42 巻 ( 1 ) 頁： 8 2022年1月

Enhancement of protein thermostability by three consecutive mutations using loop-walking method and machine learning 査読有り

Yoshida Kazunori, Kawai Shun, Fujitani Masaya, Koikeda Satoshi, Kato Ryuji, Ema Tadashi

SCIENTIFIC REPORTS 11 巻 ( 1 ) 頁： 11883 2021年6月

Predicting quality decay in continuously passaged mesenchymal stem cells by detecting morphological anomalies.  査読有り

Takemoto Yuto, Imai Yuta, Kanie Kei, Kato Ryuji

JOURNAL OF BIOSCIENCE AND BIOENGINEERING 131 巻 ( 2 ) 頁： 198 - 206 2021年2月

　前のページ - 次のページ　

<加藤 竜司>

論文 - 加藤 竜司

<加藤　竜司>

論文 - 加藤　竜司