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Rapid induction and long-term self-renewal of neural crest-derived ectodermal chondrogenic cells from hPSCs

Articular cartilage is highly specific and has limited capacity for regeneration if damaged. Human pluripotent stem cells (hPSCs) have the potential to generate any cell type in the body. Here, we report the dual-phase induction of ectodermal chondrogenic cells (ECCs) from hPSCs through the neural c...

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Autores principales: Shen, Pei, Chen, Lu, Zhang, Dahe, Xia, Simo, Lv, Zhuman, Zou, Duohong, Zhang, Zhiyuan, Yang, Chi, Li, Wenlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729200/
https://www.ncbi.nlm.nih.gov/pubmed/36477591
http://dx.doi.org/10.1038/s41536-022-00265-0
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author Shen, Pei
Chen, Lu
Zhang, Dahe
Xia, Simo
Lv, Zhuman
Zou, Duohong
Zhang, Zhiyuan
Yang, Chi
Li, Wenlin
author_facet Shen, Pei
Chen, Lu
Zhang, Dahe
Xia, Simo
Lv, Zhuman
Zou, Duohong
Zhang, Zhiyuan
Yang, Chi
Li, Wenlin
author_sort Shen, Pei
collection PubMed
description Articular cartilage is highly specific and has limited capacity for regeneration if damaged. Human pluripotent stem cells (hPSCs) have the potential to generate any cell type in the body. Here, we report the dual-phase induction of ectodermal chondrogenic cells (ECCs) from hPSCs through the neural crest (NC). ECCs were able to self-renew long-term (over numerous passages) in a cocktail of growth factors and small molecules. The cells stably expressed cranial neural crest-derived mandibular condylar cartilage markers, such as MSX1, FOXC1 and FOXC2. Compared with chondroprogenitors from iPSCs via the paraxial mesoderm, ECCs had single-cell transcriptome profiles similar to condylar chondrocytes. After the removal of the cocktail sustaining self-renewal, the cells stopped proliferating and differentiated into a homogenous chondrocyte population. Remarkably, after transplantation, this cell lineage was able to form cartilage-like structures resembling mandibular condylar cartilage in vivo. This finding provides a framework to generate self-renewing cranial chondrogenic progenitors, which could be useful for developing cell-based therapy for cranial cartilage injury.
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spelling pubmed-97292002022-12-09 Rapid induction and long-term self-renewal of neural crest-derived ectodermal chondrogenic cells from hPSCs Shen, Pei Chen, Lu Zhang, Dahe Xia, Simo Lv, Zhuman Zou, Duohong Zhang, Zhiyuan Yang, Chi Li, Wenlin NPJ Regen Med Article Articular cartilage is highly specific and has limited capacity for regeneration if damaged. Human pluripotent stem cells (hPSCs) have the potential to generate any cell type in the body. Here, we report the dual-phase induction of ectodermal chondrogenic cells (ECCs) from hPSCs through the neural crest (NC). ECCs were able to self-renew long-term (over numerous passages) in a cocktail of growth factors and small molecules. The cells stably expressed cranial neural crest-derived mandibular condylar cartilage markers, such as MSX1, FOXC1 and FOXC2. Compared with chondroprogenitors from iPSCs via the paraxial mesoderm, ECCs had single-cell transcriptome profiles similar to condylar chondrocytes. After the removal of the cocktail sustaining self-renewal, the cells stopped proliferating and differentiated into a homogenous chondrocyte population. Remarkably, after transplantation, this cell lineage was able to form cartilage-like structures resembling mandibular condylar cartilage in vivo. This finding provides a framework to generate self-renewing cranial chondrogenic progenitors, which could be useful for developing cell-based therapy for cranial cartilage injury. Nature Publishing Group UK 2022-12-08 /pmc/articles/PMC9729200/ /pubmed/36477591 http://dx.doi.org/10.1038/s41536-022-00265-0 Text en © The Author(s) 2022 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
Shen, Pei
Chen, Lu
Zhang, Dahe
Xia, Simo
Lv, Zhuman
Zou, Duohong
Zhang, Zhiyuan
Yang, Chi
Li, Wenlin
Rapid induction and long-term self-renewal of neural crest-derived ectodermal chondrogenic cells from hPSCs
title Rapid induction and long-term self-renewal of neural crest-derived ectodermal chondrogenic cells from hPSCs
title_full Rapid induction and long-term self-renewal of neural crest-derived ectodermal chondrogenic cells from hPSCs
title_fullStr Rapid induction and long-term self-renewal of neural crest-derived ectodermal chondrogenic cells from hPSCs
title_full_unstemmed Rapid induction and long-term self-renewal of neural crest-derived ectodermal chondrogenic cells from hPSCs
title_short Rapid induction and long-term self-renewal of neural crest-derived ectodermal chondrogenic cells from hPSCs
title_sort rapid induction and long-term self-renewal of neural crest-derived ectodermal chondrogenic cells from hpscs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729200/
https://www.ncbi.nlm.nih.gov/pubmed/36477591
http://dx.doi.org/10.1038/s41536-022-00265-0
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