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Definitive Endodermal Cells Supply an in vitro Source of Mesenchymal Stem/Stromal Cells

Mesenchymal stem/Stromal cells (MSCs) have great therapeutic potentials, and they have been isolated from various tissues and organs including definitive endoderm (DE) organs, such as the lung, liver and intestine. MSCs have been induced from human pluripotent stem cells (hPSCs) through multiple emb...

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Autores principales: Zhang, Yumeng, Yi, Ye, Xiao, Xia, Hu, Lingling, Xu, Jiaqi, Zheng, Dejin, Koc, Ho Cheng, Chan, Un In, Meng, Ya, Lu, Ligong, Liu, Weiwei, Xu, Xiaoling, Shao, Ningyi, Cheung, Edwin Chong Wing, Xu, Ren-He, Chen, Guokai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10151361/
https://www.ncbi.nlm.nih.gov/pubmed/37127734
http://dx.doi.org/10.1038/s42003-023-04810-5
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author Zhang, Yumeng
Yi, Ye
Xiao, Xia
Hu, Lingling
Xu, Jiaqi
Zheng, Dejin
Koc, Ho Cheng
Chan, Un In
Meng, Ya
Lu, Ligong
Liu, Weiwei
Xu, Xiaoling
Shao, Ningyi
Cheung, Edwin Chong Wing
Xu, Ren-He
Chen, Guokai
author_facet Zhang, Yumeng
Yi, Ye
Xiao, Xia
Hu, Lingling
Xu, Jiaqi
Zheng, Dejin
Koc, Ho Cheng
Chan, Un In
Meng, Ya
Lu, Ligong
Liu, Weiwei
Xu, Xiaoling
Shao, Ningyi
Cheung, Edwin Chong Wing
Xu, Ren-He
Chen, Guokai
author_sort Zhang, Yumeng
collection PubMed
description Mesenchymal stem/Stromal cells (MSCs) have great therapeutic potentials, and they have been isolated from various tissues and organs including definitive endoderm (DE) organs, such as the lung, liver and intestine. MSCs have been induced from human pluripotent stem cells (hPSCs) through multiple embryonic lineages, including the mesoderm, neural crest, and extraembryonic cells. However, it remains unclear whether hPSCs could give rise to MSCs in vitro through the endodermal lineage. Here, we report that hPSC-derived, SOX17(+) definitive endoderm progenitors can further differentiate to cells expressing classic MSC markers, which we name definitive endoderm-derived MSCs (DE-MSCs). Single cell RNA sequencing demonstrates the stepwise emergence of DE-MSCs, while endoderm-specific gene expression can be elevated by signaling modulation. DE-MSCs display multipotency and immunomodulatory activity in vitro and possess therapeutic effects in a mouse ulcerative colitis model. This study reveals that, in addition to the other germ layers, the definitive endoderm can also contribute to MSCs and DE-MSCs could be a cell source for regenerative medicine.
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spelling pubmed-101513612023-05-03 Definitive Endodermal Cells Supply an in vitro Source of Mesenchymal Stem/Stromal Cells Zhang, Yumeng Yi, Ye Xiao, Xia Hu, Lingling Xu, Jiaqi Zheng, Dejin Koc, Ho Cheng Chan, Un In Meng, Ya Lu, Ligong Liu, Weiwei Xu, Xiaoling Shao, Ningyi Cheung, Edwin Chong Wing Xu, Ren-He Chen, Guokai Commun Biol Article Mesenchymal stem/Stromal cells (MSCs) have great therapeutic potentials, and they have been isolated from various tissues and organs including definitive endoderm (DE) organs, such as the lung, liver and intestine. MSCs have been induced from human pluripotent stem cells (hPSCs) through multiple embryonic lineages, including the mesoderm, neural crest, and extraembryonic cells. However, it remains unclear whether hPSCs could give rise to MSCs in vitro through the endodermal lineage. Here, we report that hPSC-derived, SOX17(+) definitive endoderm progenitors can further differentiate to cells expressing classic MSC markers, which we name definitive endoderm-derived MSCs (DE-MSCs). Single cell RNA sequencing demonstrates the stepwise emergence of DE-MSCs, while endoderm-specific gene expression can be elevated by signaling modulation. DE-MSCs display multipotency and immunomodulatory activity in vitro and possess therapeutic effects in a mouse ulcerative colitis model. This study reveals that, in addition to the other germ layers, the definitive endoderm can also contribute to MSCs and DE-MSCs could be a cell source for regenerative medicine. Nature Publishing Group UK 2023-05-01 /pmc/articles/PMC10151361/ /pubmed/37127734 http://dx.doi.org/10.1038/s42003-023-04810-5 Text en © The Author(s) 2023 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
Zhang, Yumeng
Yi, Ye
Xiao, Xia
Hu, Lingling
Xu, Jiaqi
Zheng, Dejin
Koc, Ho Cheng
Chan, Un In
Meng, Ya
Lu, Ligong
Liu, Weiwei
Xu, Xiaoling
Shao, Ningyi
Cheung, Edwin Chong Wing
Xu, Ren-He
Chen, Guokai
Definitive Endodermal Cells Supply an in vitro Source of Mesenchymal Stem/Stromal Cells
title Definitive Endodermal Cells Supply an in vitro Source of Mesenchymal Stem/Stromal Cells
title_full Definitive Endodermal Cells Supply an in vitro Source of Mesenchymal Stem/Stromal Cells
title_fullStr Definitive Endodermal Cells Supply an in vitro Source of Mesenchymal Stem/Stromal Cells
title_full_unstemmed Definitive Endodermal Cells Supply an in vitro Source of Mesenchymal Stem/Stromal Cells
title_short Definitive Endodermal Cells Supply an in vitro Source of Mesenchymal Stem/Stromal Cells
title_sort definitive endodermal cells supply an in vitro source of mesenchymal stem/stromal cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10151361/
https://www.ncbi.nlm.nih.gov/pubmed/37127734
http://dx.doi.org/10.1038/s42003-023-04810-5
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