miR-142-3p Contributes to Early Cardiac Fate Decision of Embryonic Stem Cells

MicroRNAs (miRNAs) play important roles in cell fate decisions. However, the miRNAs and their targets involved in the regulation of cardiac lineage specification are largely unexplored. Here, we report novel functions of miR-142-3p in the regulation of cardiomyocyte differentiation from mouse embryo...

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Main Authors: Zhong-Yan Chen, Fei Chen, Nan Cao, Zhi-Wen Zhou, Huang-Tian Yang
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2017/1769298
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author Zhong-Yan Chen
Fei Chen
Nan Cao
Zhi-Wen Zhou
Huang-Tian Yang
author_facet Zhong-Yan Chen
Fei Chen
Nan Cao
Zhi-Wen Zhou
Huang-Tian Yang
author_sort Zhong-Yan Chen
collection DOAJ
description MicroRNAs (miRNAs) play important roles in cell fate decisions. However, the miRNAs and their targets involved in the regulation of cardiac lineage specification are largely unexplored. Here, we report novel functions of miR-142-3p in the regulation of cardiomyocyte differentiation from mouse embryonic stem cells (mESCs). With a miRNA array screen, we identified a number of miRNAs significantly changed during mESC differentiation into the mesodermal and cardiac progenitor cells, and miR-142-3p was one among the markedly downregulated miRNAs. Ectopic expression and inhibition of miR-142-3p did not alter the characteristics of undifferentiated ESCs, whereas ectopic expression of miR-142-3p impaired cardiomyocyte formation. In addition, ectopic expression of miR-142-3p inhibited the expression of a cardiac mesodermal marker gene Mesp1 and downstream cardiac transcription factors Nkx2.5, Tbx5, and Mef2c but not the expression of three germ layer-specific genes. We further demonstrated that miR-142-3p targeted the 3′-untranslated region of Mef2c. These results reveal miR-142-3p as an important regulator of early cardiomyocyte differentiation. Our findings provide new knowledge for further understanding of roles and mechanisms of miRNAs as critical regulators of cardiomyocyte differentiation.
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institution Kabale University
issn 1687-966X
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publishDate 2017-01-01
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series Stem Cells International
spelling doaj-art-77914f4ed9b7468882309cfb6581bee72025-02-03T07:25:34ZengWileyStem Cells International1687-966X1687-96782017-01-01201710.1155/2017/17692981769298miR-142-3p Contributes to Early Cardiac Fate Decision of Embryonic Stem CellsZhong-Yan Chen0Fei Chen1Nan Cao2Zhi-Wen Zhou3Huang-Tian Yang4Key Laboratory of Stem Cell Biology and Laboratory of Molecular Cardiology, Institute of Health Sciences, Shanghai Jiao Tong University School of Medicine (SJTUSM) and Shanghai Institutes for Biological Sciences (SIBS), Chinese Academy of Sciences (CAS), Shanghai, ChinaKey Laboratory of Stem Cell Biology and Laboratory of Molecular Cardiology, Institute of Health Sciences, Shanghai Jiao Tong University School of Medicine (SJTUSM) and Shanghai Institutes for Biological Sciences (SIBS), Chinese Academy of Sciences (CAS), Shanghai, ChinaKey Laboratory of Stem Cell Biology and Laboratory of Molecular Cardiology, Institute of Health Sciences, Shanghai Jiao Tong University School of Medicine (SJTUSM) and Shanghai Institutes for Biological Sciences (SIBS), Chinese Academy of Sciences (CAS), Shanghai, ChinaDepartment of Cardiology, Shanghai Xuhui District Central Hospital, Shanghai, ChinaKey Laboratory of Stem Cell Biology and Laboratory of Molecular Cardiology, Institute of Health Sciences, Shanghai Jiao Tong University School of Medicine (SJTUSM) and Shanghai Institutes for Biological Sciences (SIBS), Chinese Academy of Sciences (CAS), Shanghai, ChinaMicroRNAs (miRNAs) play important roles in cell fate decisions. However, the miRNAs and their targets involved in the regulation of cardiac lineage specification are largely unexplored. Here, we report novel functions of miR-142-3p in the regulation of cardiomyocyte differentiation from mouse embryonic stem cells (mESCs). With a miRNA array screen, we identified a number of miRNAs significantly changed during mESC differentiation into the mesodermal and cardiac progenitor cells, and miR-142-3p was one among the markedly downregulated miRNAs. Ectopic expression and inhibition of miR-142-3p did not alter the characteristics of undifferentiated ESCs, whereas ectopic expression of miR-142-3p impaired cardiomyocyte formation. In addition, ectopic expression of miR-142-3p inhibited the expression of a cardiac mesodermal marker gene Mesp1 and downstream cardiac transcription factors Nkx2.5, Tbx5, and Mef2c but not the expression of three germ layer-specific genes. We further demonstrated that miR-142-3p targeted the 3′-untranslated region of Mef2c. These results reveal miR-142-3p as an important regulator of early cardiomyocyte differentiation. Our findings provide new knowledge for further understanding of roles and mechanisms of miRNAs as critical regulators of cardiomyocyte differentiation.http://dx.doi.org/10.1155/2017/1769298
spellingShingle Zhong-Yan Chen
Fei Chen
Nan Cao
Zhi-Wen Zhou
Huang-Tian Yang
miR-142-3p Contributes to Early Cardiac Fate Decision of Embryonic Stem Cells
Stem Cells International
title miR-142-3p Contributes to Early Cardiac Fate Decision of Embryonic Stem Cells
title_full miR-142-3p Contributes to Early Cardiac Fate Decision of Embryonic Stem Cells
title_fullStr miR-142-3p Contributes to Early Cardiac Fate Decision of Embryonic Stem Cells
title_full_unstemmed miR-142-3p Contributes to Early Cardiac Fate Decision of Embryonic Stem Cells
title_short miR-142-3p Contributes to Early Cardiac Fate Decision of Embryonic Stem Cells
title_sort mir 142 3p contributes to early cardiac fate decision of embryonic stem cells
url http://dx.doi.org/10.1155/2017/1769298
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AT feichen mir1423pcontributestoearlycardiacfatedecisionofembryonicstemcells
AT nancao mir1423pcontributestoearlycardiacfatedecisionofembryonicstemcells
AT zhiwenzhou mir1423pcontributestoearlycardiacfatedecisionofembryonicstemcells
AT huangtianyang mir1423pcontributestoearlycardiacfatedecisionofembryonicstemcells