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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...

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Autores principales: Zhang, Yiqiang, Zhong, Jiang F, Qiu, Hongyu, Robb MacLellan, W., Marbán, Eduardo, Wang, Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
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.
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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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