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 |
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タイトル |
Capacity of Retinal Ganglion Cells Derived from Human Induced Pluripotent Stem Cells to Suppress T-Cells |
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言語 |
en |
作成者 |
Edo, Ayaka
Sugita, Sunao
Futatsugi, Yoko
Sho, Junki
Onishi, Akishi
Kiuchi, Yoshiaki
Takahashi, Masayo
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アクセス権 |
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アクセス権 |
open access |
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アクセス権URI |
http://purl.org/coar/access_right/c_abf2 |
権利情報 |
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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 |
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主題Scheme |
Other |
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主題 |
retinal ganglion cells |
主題 |
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主題Scheme |
Other |
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主題 |
induced pluripotent stem cells |
主題 |
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主題Scheme |
Other |
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主題 |
immunogenicity |
主題 |
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主題Scheme |
Other |
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主題 |
mixed lymphocyte reaction |
主題 |
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主題Scheme |
Other |
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主題 |
immunosuppression |
内容記述 |
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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. |
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言語 |
en |
内容記述 |
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内容記述タイプ |
Other |
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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 |
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出版者 |
MDPI |
言語 |
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言語 |
eng |
資源タイプ |
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資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
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資源タイプ |
journal article |
出版タイプ |
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出版タイプ |
VoR |
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出版タイプResource |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
関連情報 |
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識別子タイプ |
DOI |
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関連識別子 |
10.3390/ijms21217831 |
関連情報 |
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識別子タイプ |
DOI |
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関連識別子 |
https://doi.org/10.3390/ijms21217831 |
収録物識別子 |
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収録物識別子タイプ |
ISSN |
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収録物識別子 |
1661-6596 |
収録物識別子 |
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収録物識別子タイプ |
ISSN |
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収録物識別子 |
1422-0067 |
開始ページ |
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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
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旧ID |
51560 |