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Hypoxia promotes a perinatal-like progenitor state in the adult murine epicardium
The epicardium is a reservoir of progenitors that give rise to coronary vasculature and stroma during development and mediates cardiac vascular repair. However, its role as a source of progenitors in the adult mammalian heart remains unclear due to lack of clear lineage markers and single-cell cultu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166725/ https://www.ncbi.nlm.nih.gov/pubmed/35661120 http://dx.doi.org/10.1038/s41598-022-13107-2 |
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author | Sayed, Angeliqua Turoczi, Szimonetta Soares-da-Silva, Francisca Marazzi, Giovanna Hulot, Jean-Sebastien Sassoon, David Valente, Mariana |
author_facet | Sayed, Angeliqua Turoczi, Szimonetta Soares-da-Silva, Francisca Marazzi, Giovanna Hulot, Jean-Sebastien Sassoon, David Valente, Mariana |
author_sort | Sayed, Angeliqua |
collection | PubMed |
description | The epicardium is a reservoir of progenitors that give rise to coronary vasculature and stroma during development and mediates cardiac vascular repair. However, its role as a source of progenitors in the adult mammalian heart remains unclear due to lack of clear lineage markers and single-cell culture systems to elucidate epicardial progeny cell fate. We found that in vivo exposure of mice to physiological hypoxia induced adult epicardial cells to re-enter the cell cycle and to express a subset of developmental genes. Multiplex single cell transcriptional profiling revealed a lineage relationship between epicardial cells and smooth muscle, stromal cells, as well as cells with an endothelial-like fate. We found that physiological hypoxia promoted a perinatal-like progenitor state in the adult murine epicardium. In vitro clonal analyses of purified epicardial cells showed that cell growth and subsequent differentiation is dependent upon hypoxia, and that resident epicardial cells retain progenitor identity in the adult mammalian heart with self-renewal and multilineage differentiation potential. These results point to a source of progenitor cells in the adult heart that can be stimulated in vivo and provide an in vitro model for further studies. |
format | Online Article Text |
id | pubmed-9166725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91667252022-06-05 Hypoxia promotes a perinatal-like progenitor state in the adult murine epicardium Sayed, Angeliqua Turoczi, Szimonetta Soares-da-Silva, Francisca Marazzi, Giovanna Hulot, Jean-Sebastien Sassoon, David Valente, Mariana Sci Rep Article The epicardium is a reservoir of progenitors that give rise to coronary vasculature and stroma during development and mediates cardiac vascular repair. However, its role as a source of progenitors in the adult mammalian heart remains unclear due to lack of clear lineage markers and single-cell culture systems to elucidate epicardial progeny cell fate. We found that in vivo exposure of mice to physiological hypoxia induced adult epicardial cells to re-enter the cell cycle and to express a subset of developmental genes. Multiplex single cell transcriptional profiling revealed a lineage relationship between epicardial cells and smooth muscle, stromal cells, as well as cells with an endothelial-like fate. We found that physiological hypoxia promoted a perinatal-like progenitor state in the adult murine epicardium. In vitro clonal analyses of purified epicardial cells showed that cell growth and subsequent differentiation is dependent upon hypoxia, and that resident epicardial cells retain progenitor identity in the adult mammalian heart with self-renewal and multilineage differentiation potential. These results point to a source of progenitor cells in the adult heart that can be stimulated in vivo and provide an in vitro model for further studies. Nature Publishing Group UK 2022-06-03 /pmc/articles/PMC9166725/ /pubmed/35661120 http://dx.doi.org/10.1038/s41598-022-13107-2 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sayed, Angeliqua Turoczi, Szimonetta Soares-da-Silva, Francisca Marazzi, Giovanna Hulot, Jean-Sebastien Sassoon, David Valente, Mariana Hypoxia promotes a perinatal-like progenitor state in the adult murine epicardium |
title | Hypoxia promotes a perinatal-like progenitor state in the adult murine epicardium |
title_full | Hypoxia promotes a perinatal-like progenitor state in the adult murine epicardium |
title_fullStr | Hypoxia promotes a perinatal-like progenitor state in the adult murine epicardium |
title_full_unstemmed | Hypoxia promotes a perinatal-like progenitor state in the adult murine epicardium |
title_short | Hypoxia promotes a perinatal-like progenitor state in the adult murine epicardium |
title_sort | hypoxia promotes a perinatal-like progenitor state in the adult murine epicardium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166725/ https://www.ncbi.nlm.nih.gov/pubmed/35661120 http://dx.doi.org/10.1038/s41598-022-13107-2 |
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