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Efficient generation of thymic epithelium from induced pluripotent stem cells that prolongs allograft survival
The thymus plays a significant role in establishing immunological self-tolerance. Previous studies have revealed that host immune reaction to allogeneic transplants could be regulated by thymus transplantation. However, physiological thymus involution hinders the clinical application of these insigh...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959230/ https://www.ncbi.nlm.nih.gov/pubmed/31937817 http://dx.doi.org/10.1038/s41598-019-57088-1 |
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author | Otsuka, Ryo Wada, Haruka Tsuji, Hyuma Sasaki, Airi Murata, Tomoki Itoh, Mizuho Baghdadi, Muhammad Seino, Ken-ichiro |
author_facet | Otsuka, Ryo Wada, Haruka Tsuji, Hyuma Sasaki, Airi Murata, Tomoki Itoh, Mizuho Baghdadi, Muhammad Seino, Ken-ichiro |
author_sort | Otsuka, Ryo |
collection | PubMed |
description | The thymus plays a significant role in establishing immunological self-tolerance. Previous studies have revealed that host immune reaction to allogeneic transplants could be regulated by thymus transplantation. However, physiological thymus involution hinders the clinical application of these insights. Here, we report an efficient generation of thymic epithelial-like tissue derived from induced pluripotent stem cells (iPSCs) and its potential to regulate immune reaction in allogeneic transplantation. We established an iPSC line which constitutively expresses mouse Foxn1 gene and examined the effect of its expression during in vitro differentiation of thymic epithelial cells (TECs). We found that Foxn1 expression enhances the differentiation induction of cells expressing TEC-related cell surface molecules along with upregulation of endogenous Foxn1. iPSC-derived TECs (iPSC-TECs) generated T cells in nude recipient mice after renal subcapsular transplantation. Moreover, iPSC-TEC transplantation to immuno-competent recipients significantly prolonged the survival of allogeneic skin. Our study provides a novel concept for allogeneic transplantation in the setting of regenerative medicine. |
format | Online Article Text |
id | pubmed-6959230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69592302020-01-16 Efficient generation of thymic epithelium from induced pluripotent stem cells that prolongs allograft survival Otsuka, Ryo Wada, Haruka Tsuji, Hyuma Sasaki, Airi Murata, Tomoki Itoh, Mizuho Baghdadi, Muhammad Seino, Ken-ichiro Sci Rep Article The thymus plays a significant role in establishing immunological self-tolerance. Previous studies have revealed that host immune reaction to allogeneic transplants could be regulated by thymus transplantation. However, physiological thymus involution hinders the clinical application of these insights. Here, we report an efficient generation of thymic epithelial-like tissue derived from induced pluripotent stem cells (iPSCs) and its potential to regulate immune reaction in allogeneic transplantation. We established an iPSC line which constitutively expresses mouse Foxn1 gene and examined the effect of its expression during in vitro differentiation of thymic epithelial cells (TECs). We found that Foxn1 expression enhances the differentiation induction of cells expressing TEC-related cell surface molecules along with upregulation of endogenous Foxn1. iPSC-derived TECs (iPSC-TECs) generated T cells in nude recipient mice after renal subcapsular transplantation. Moreover, iPSC-TEC transplantation to immuno-competent recipients significantly prolonged the survival of allogeneic skin. Our study provides a novel concept for allogeneic transplantation in the setting of regenerative medicine. Nature Publishing Group UK 2020-01-14 /pmc/articles/PMC6959230/ /pubmed/31937817 http://dx.doi.org/10.1038/s41598-019-57088-1 Text en © The Author(s) 2020, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Otsuka, Ryo Wada, Haruka Tsuji, Hyuma Sasaki, Airi Murata, Tomoki Itoh, Mizuho Baghdadi, Muhammad Seino, Ken-ichiro Efficient generation of thymic epithelium from induced pluripotent stem cells that prolongs allograft survival |
title | Efficient generation of thymic epithelium from induced pluripotent stem cells that prolongs allograft survival |
title_full | Efficient generation of thymic epithelium from induced pluripotent stem cells that prolongs allograft survival |
title_fullStr | Efficient generation of thymic epithelium from induced pluripotent stem cells that prolongs allograft survival |
title_full_unstemmed | Efficient generation of thymic epithelium from induced pluripotent stem cells that prolongs allograft survival |
title_short | Efficient generation of thymic epithelium from induced pluripotent stem cells that prolongs allograft survival |
title_sort | efficient generation of thymic epithelium from induced pluripotent stem cells that prolongs allograft survival |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959230/ https://www.ncbi.nlm.nih.gov/pubmed/31937817 http://dx.doi.org/10.1038/s41598-019-57088-1 |
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