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Induction of macrophage-like immunosuppressive cells from common marmoset ES cells by stepwise differentiation with DZNep
Recent progress in regenerative medicine has enabled the utilization of pluripotent stem cells (PSCs) as the resource of therapeutic cells/tissue. However, immune suppression is still needed when the donor–recipient combination is allogeneic. We have reported previously that mouse PSCs-derived immun...
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/PMC7387549/ https://www.ncbi.nlm.nih.gov/pubmed/32724084 http://dx.doi.org/10.1038/s41598-020-69690-9 |
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author | Tsuji, Hyuma Otsuka, Ryo Wada, Haruka Murata, Tomoki Sasaki, Airi Itoh, Mizuho Baghdadi, Muhammad Sasaki, Erika Seino, Ken-ichiro |
author_facet | Tsuji, Hyuma Otsuka, Ryo Wada, Haruka Murata, Tomoki Sasaki, Airi Itoh, Mizuho Baghdadi, Muhammad Sasaki, Erika Seino, Ken-ichiro |
author_sort | Tsuji, Hyuma |
collection | PubMed |
description | Recent progress in regenerative medicine has enabled the utilization of pluripotent stem cells (PSCs) as the resource of therapeutic cells/tissue. However, immune suppression is still needed when the donor–recipient combination is allogeneic. We have reported previously that mouse PSCs-derived immunosuppressive cells contribute to prolonged survival of grafts derived from the same mouse PSCs in allogeneic recipients. For its clinical application, a preclinical study using non-human primates such as common marmoset must be performed. In this study, we established the induction protocol of immunosuppressive cells from common marmoset ES cells. Although similar immunosuppressive macrophages could not be induced by same protocol as that for mouse PSCs, we employed an inhibitor for histone methyltransferase, DZNep, and succeeded to induce them. The DZNep-treated macrophage-like cells expressed several immunosuppressive molecules and significantly inhibited allogeneic mixed lymphocyte reaction. The immunosuppressive cells from non-human primate ESCs will help to establish an immunoregulating strategy in regenerative medicine using PSCs. |
format | Online Article Text |
id | pubmed-7387549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73875492020-07-29 Induction of macrophage-like immunosuppressive cells from common marmoset ES cells by stepwise differentiation with DZNep Tsuji, Hyuma Otsuka, Ryo Wada, Haruka Murata, Tomoki Sasaki, Airi Itoh, Mizuho Baghdadi, Muhammad Sasaki, Erika Seino, Ken-ichiro Sci Rep Article Recent progress in regenerative medicine has enabled the utilization of pluripotent stem cells (PSCs) as the resource of therapeutic cells/tissue. However, immune suppression is still needed when the donor–recipient combination is allogeneic. We have reported previously that mouse PSCs-derived immunosuppressive cells contribute to prolonged survival of grafts derived from the same mouse PSCs in allogeneic recipients. For its clinical application, a preclinical study using non-human primates such as common marmoset must be performed. In this study, we established the induction protocol of immunosuppressive cells from common marmoset ES cells. Although similar immunosuppressive macrophages could not be induced by same protocol as that for mouse PSCs, we employed an inhibitor for histone methyltransferase, DZNep, and succeeded to induce them. The DZNep-treated macrophage-like cells expressed several immunosuppressive molecules and significantly inhibited allogeneic mixed lymphocyte reaction. The immunosuppressive cells from non-human primate ESCs will help to establish an immunoregulating strategy in regenerative medicine using PSCs. Nature Publishing Group UK 2020-07-28 /pmc/articles/PMC7387549/ /pubmed/32724084 http://dx.doi.org/10.1038/s41598-020-69690-9 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Tsuji, Hyuma Otsuka, Ryo Wada, Haruka Murata, Tomoki Sasaki, Airi Itoh, Mizuho Baghdadi, Muhammad Sasaki, Erika Seino, Ken-ichiro Induction of macrophage-like immunosuppressive cells from common marmoset ES cells by stepwise differentiation with DZNep |
title | Induction of macrophage-like immunosuppressive cells from common marmoset ES cells by stepwise differentiation with DZNep |
title_full | Induction of macrophage-like immunosuppressive cells from common marmoset ES cells by stepwise differentiation with DZNep |
title_fullStr | Induction of macrophage-like immunosuppressive cells from common marmoset ES cells by stepwise differentiation with DZNep |
title_full_unstemmed | Induction of macrophage-like immunosuppressive cells from common marmoset ES cells by stepwise differentiation with DZNep |
title_short | Induction of macrophage-like immunosuppressive cells from common marmoset ES cells by stepwise differentiation with DZNep |
title_sort | induction of macrophage-like immunosuppressive cells from common marmoset es cells by stepwise differentiation with dznep |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387549/ https://www.ncbi.nlm.nih.gov/pubmed/32724084 http://dx.doi.org/10.1038/s41598-020-69690-9 |
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