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Epigenomic Reprogramming of Adult Cardiomyocyte-Derived Cardiac Progenitor Cells
It has been believed that mammalian adult cardiomyocytes (ACMs) are terminally-differentiated and are unable to proliferate. Recently, using a bi-transgenic ACM fate mapping mouse model and an in vitro culture system, we demonstrated that adult mouse cardiomyocytes were able to dedifferentiate into...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677315/ https://www.ncbi.nlm.nih.gov/pubmed/26657817 http://dx.doi.org/10.1038/srep17686 |
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author | Zhang, Yiqiang Zhong, Jiang F Qiu, Hongyu Robb MacLellan, W. Marbán, Eduardo Wang, Charles |
author_facet | Zhang, Yiqiang Zhong, Jiang F Qiu, Hongyu Robb MacLellan, W. Marbán, Eduardo Wang, Charles |
author_sort | Zhang, Yiqiang |
collection | PubMed |
description | It has been believed that mammalian adult cardiomyocytes (ACMs) are terminally-differentiated and are unable to proliferate. Recently, using a bi-transgenic ACM fate mapping mouse model and an in vitro culture system, we demonstrated that adult mouse cardiomyocytes were able to dedifferentiate into cardiac progenitor-like cells (CPCs). However, little is known about the molecular basis of their intrinsic cellular plasticity. Here we integrate single-cell transcriptome and whole-genome DNA methylation analyses to unravel the molecular mechanisms underlying the dedifferentiation and cell cycle reentry of mouse ACMs. Compared to parental cardiomyocytes, dedifferentiated mouse cardiomyocyte-derived CPCs (mCPCs) display epigenomic reprogramming with many differentially-methylated regions, both hypermethylated and hypomethylated, across the entire genome. Correlated well with the methylome, our transcriptomic data showed that the genes encoding cardiac structure and function proteins are remarkably down-regulated in mCPCs, while those for cell cycle, proliferation, and stemness are significantly up-regulated. In addition, implantation of mCPCs into infarcted mouse myocardium improves cardiac function with augmented left ventricular ejection fraction. Our study demonstrates that the cellular plasticity of mammalian cardiomyocytes is the result of a well-orchestrated epigenomic reprogramming and a subsequent global transcriptomic alteration. |
format | Online Article Text |
id | pubmed-4677315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46773152015-12-17 Epigenomic Reprogramming of Adult Cardiomyocyte-Derived Cardiac Progenitor Cells Zhang, Yiqiang Zhong, Jiang F Qiu, Hongyu Robb MacLellan, W. Marbán, Eduardo Wang, Charles Sci Rep Article It has been believed that mammalian adult cardiomyocytes (ACMs) are terminally-differentiated and are unable to proliferate. Recently, using a bi-transgenic ACM fate mapping mouse model and an in vitro culture system, we demonstrated that adult mouse cardiomyocytes were able to dedifferentiate into cardiac progenitor-like cells (CPCs). However, little is known about the molecular basis of their intrinsic cellular plasticity. Here we integrate single-cell transcriptome and whole-genome DNA methylation analyses to unravel the molecular mechanisms underlying the dedifferentiation and cell cycle reentry of mouse ACMs. Compared to parental cardiomyocytes, dedifferentiated mouse cardiomyocyte-derived CPCs (mCPCs) display epigenomic reprogramming with many differentially-methylated regions, both hypermethylated and hypomethylated, across the entire genome. Correlated well with the methylome, our transcriptomic data showed that the genes encoding cardiac structure and function proteins are remarkably down-regulated in mCPCs, while those for cell cycle, proliferation, and stemness are significantly up-regulated. In addition, implantation of mCPCs into infarcted mouse myocardium improves cardiac function with augmented left ventricular ejection fraction. Our study demonstrates that the cellular plasticity of mammalian cardiomyocytes is the result of a well-orchestrated epigenomic reprogramming and a subsequent global transcriptomic alteration. Nature Publishing Group 2015-12-14 /pmc/articles/PMC4677315/ /pubmed/26657817 http://dx.doi.org/10.1038/srep17686 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zhang, Yiqiang Zhong, Jiang F Qiu, Hongyu Robb MacLellan, W. Marbán, Eduardo Wang, Charles Epigenomic Reprogramming of Adult Cardiomyocyte-Derived Cardiac Progenitor Cells |
title | Epigenomic Reprogramming of Adult Cardiomyocyte-Derived Cardiac Progenitor Cells |
title_full | Epigenomic Reprogramming of Adult Cardiomyocyte-Derived Cardiac Progenitor Cells |
title_fullStr | Epigenomic Reprogramming of Adult Cardiomyocyte-Derived Cardiac Progenitor Cells |
title_full_unstemmed | Epigenomic Reprogramming of Adult Cardiomyocyte-Derived Cardiac Progenitor Cells |
title_short | Epigenomic Reprogramming of Adult Cardiomyocyte-Derived Cardiac Progenitor Cells |
title_sort | epigenomic reprogramming of adult cardiomyocyte-derived cardiac progenitor cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677315/ https://www.ncbi.nlm.nih.gov/pubmed/26657817 http://dx.doi.org/10.1038/srep17686 |
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