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Capacity of Retinal Ganglion Cells Derived from Human Induced Pluripotent Stem Cells to Suppress T-Cells

https://hiroshima.repo.nii.ac.jp/records/2007121
https://hiroshima.repo.nii.ac.jp/records/2007121
354fbb36-f45f-4f0b-bcc5-eb0ff569a649
名前 / ファイル ライセンス アクション
IntJMolSci_21_7831.pdf IntJMolSci_21_7831.pdf (4.8 MB)
Item type デフォルトアイテムタイプ_(フル)(1)
公開日 2023-03-18
タイトル
タイトル Capacity of Retinal Ganglion Cells Derived from Human Induced Pluripotent Stem Cells to Suppress T-Cells
言語 en
作成者 Edo, Ayaka

× Edo, Ayaka

en Edo, Ayaka

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Sugita, Sunao

× Sugita, Sunao

en Sugita, Sunao

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Futatsugi, Yoko

× Futatsugi, Yoko

en Futatsugi, Yoko

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Sho, Junki

× Sho, Junki

en Sho, Junki

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Onishi, Akishi

× Onishi, Akishi

en Onishi, Akishi

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Kiuchi, Yoshiaki

× Kiuchi, Yoshiaki

en Kiuchi, Yoshiaki

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Takahashi, Masayo

× Takahashi, Masayo

en Takahashi, Masayo

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アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
権利情報
権利情報 © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
主題
主題Scheme Other
主題 retinal ganglion cells
主題
主題Scheme Other
主題 induced pluripotent stem cells
主題
主題Scheme Other
主題 immunogenicity
主題
主題Scheme Other
主題 mixed lymphocyte reaction
主題
主題Scheme Other
主題 immunosuppression
内容記述
内容記述 Retinal ganglion cells (RGCs) are impaired in patients such as those with glaucoma and optic neuritis, resulting in permanent vision loss. To restore visual function, development of RGC transplantation therapy is now underway. Induced pluripotent stem cells (iPSCs) are an important source of RGCs for human allogeneic transplantation. We therefore analyzed the immunological characteristics of iPSC-derived RGCs (iPSC-RGCs) to evaluate the possibility of rejection after RGC transplantation. We first assessed the expression of human leukocyte antigen (HLA) molecules on iPSC-RGCs using immunostaining, and then evaluated the effects of iPSC-RGCs to activate lymphocytes using the mixed lymphocyte reaction (MLR) and iPSC-RGC co-cultures. We observed low expression of HLA class I and no expression of HLA class II molecules on iPSC-RGCs. We also found that iPSC-RGCs strongly suppressed various inflammatory immune cells including activated T-cells in the MLR assay and that transforming growth factor-β2 produced by iPSC-RGCs played a critical role in suppression of inflammatory cells in vitro. Our data suggest that iPSC-RGCs have low immunogenicity, and immunosuppressive capacity on lymphocytes. Our study will contribute to predicting immune attacks after RGC transplantation.
言語 en
内容記述
内容記述タイプ Other
内容記述 This work was supported by the Research Center Network for Realization of Regenerative Medicine from the Japan Agency for Medical Research and Development (AMED) to M.T., and by a Scientific Research Grant (B, 18H02959) from the Ministry of Education, Culture, Sports, Science and Technology of Japan to S.S. A.E. was financially supported from RIKEN by a Junior Research Associate (JRA) program for graduate students.
出版者
出版者 MDPI
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連情報
識別子タイプ DOI
関連識別子 10.3390/ijms21217831
関連情報
識別子タイプ DOI
関連識別子 https://doi.org/10.3390/ijms21217831
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 1661-6596
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 1422-0067
開始ページ
開始ページ 7831
書誌情報 International Journal of Molecular Sciences
International Journal of Molecular Sciences

巻 21, 号 21, p. 7831, 発行日 2020-10-22
旧ID 51560
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