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Identification of mesenchymal-to-epithelial transition during heart regeneration through genetic lineage tracing
The epicardium is the important outermost mesothelial/epithelial layer of the heart that serves as a signaling center for cardiac development and repair. During heart development, epicardial cells undergo a process known as epithelial-to-mesenchymal transition to form diverse mesenchymal cell lineag...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10268380/ https://www.ncbi.nlm.nih.gov/pubmed/37316879 http://dx.doi.org/10.1186/s13287-023-03391-8 |
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author | Gao, Zibei Lu, Zhengkai Meng, Jinyan Lin, Chao-Po Zhang, Hui Tang, Juan |
author_facet | Gao, Zibei Lu, Zhengkai Meng, Jinyan Lin, Chao-Po Zhang, Hui Tang, Juan |
author_sort | Gao, Zibei |
collection | PubMed |
description | The epicardium is the important outermost mesothelial/epithelial layer of the heart that serves as a signaling center for cardiac development and repair. During heart development, epicardial cells undergo a process known as epithelial-to-mesenchymal transition to form diverse mesenchymal cell lineages, such as fibroblasts, coronary vascular smooth muscle cells, and pericytes. However, it is not clear whether the reverse process, mesenchymal-to-epithelial transition (MET), takes place in the mammalian heart. In this study, we performed apical resection on neonatal hearts and used Fap-CreER;Ai9 labeling to track activated fibroblasts in the injured cardiac regions. We found that these fibroblasts underwent MET to generate epicardial cells during heart regeneration. To our knowledge, this is the first report of MET occurring in vivo during heart development and regeneration. Our findings suggest that it is feasible to directly convert fibroblasts into epicardial cells, providing a novel approach to generate epicardial cells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03391-8. |
format | Online Article Text |
id | pubmed-10268380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102683802023-06-15 Identification of mesenchymal-to-epithelial transition during heart regeneration through genetic lineage tracing Gao, Zibei Lu, Zhengkai Meng, Jinyan Lin, Chao-Po Zhang, Hui Tang, Juan Stem Cell Res Ther Letter The epicardium is the important outermost mesothelial/epithelial layer of the heart that serves as a signaling center for cardiac development and repair. During heart development, epicardial cells undergo a process known as epithelial-to-mesenchymal transition to form diverse mesenchymal cell lineages, such as fibroblasts, coronary vascular smooth muscle cells, and pericytes. However, it is not clear whether the reverse process, mesenchymal-to-epithelial transition (MET), takes place in the mammalian heart. In this study, we performed apical resection on neonatal hearts and used Fap-CreER;Ai9 labeling to track activated fibroblasts in the injured cardiac regions. We found that these fibroblasts underwent MET to generate epicardial cells during heart regeneration. To our knowledge, this is the first report of MET occurring in vivo during heart development and regeneration. Our findings suggest that it is feasible to directly convert fibroblasts into epicardial cells, providing a novel approach to generate epicardial cells. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03391-8. BioMed Central 2023-06-14 /pmc/articles/PMC10268380/ /pubmed/37316879 http://dx.doi.org/10.1186/s13287-023-03391-8 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 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Letter Gao, Zibei Lu, Zhengkai Meng, Jinyan Lin, Chao-Po Zhang, Hui Tang, Juan Identification of mesenchymal-to-epithelial transition during heart regeneration through genetic lineage tracing |
title | Identification of mesenchymal-to-epithelial transition during heart regeneration through genetic lineage tracing |
title_full | Identification of mesenchymal-to-epithelial transition during heart regeneration through genetic lineage tracing |
title_fullStr | Identification of mesenchymal-to-epithelial transition during heart regeneration through genetic lineage tracing |
title_full_unstemmed | Identification of mesenchymal-to-epithelial transition during heart regeneration through genetic lineage tracing |
title_short | Identification of mesenchymal-to-epithelial transition during heart regeneration through genetic lineage tracing |
title_sort | identification of mesenchymal-to-epithelial transition during heart regeneration through genetic lineage tracing |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10268380/ https://www.ncbi.nlm.nih.gov/pubmed/37316879 http://dx.doi.org/10.1186/s13287-023-03391-8 |
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