mir-17–92 Cluster Is Required for and Sufficient to Induce Cardiomyocyte Proliferation in Postnatal and Adult Hearts

Jinghai Chen(Harvard Stem Cell Institute), Zhan‐Peng Huang(Harvard Stem Cell Institute), Heeyoung Seok(Harvard Stem Cell Institute), Jian Ding(Harvard Stem Cell Institute), Masaharu Kataoka(Harvard Stem Cell Institute), Zheng Zhang(Harvard Stem Cell Institute), Xiaoyun Hu(Harvard Stem Cell Institute), Gang Wang(Harvard Stem Cell Institute), Zhiqiang Lin(Harvard Stem Cell Institute), Si Wang(Harvard Stem Cell Institute), William T. Pu(Harvard Stem Cell Institute), Ronglih Liao(Harvard Stem Cell Institute), Da‐Zhi Wang(Harvard Stem Cell Institute)
Circulation Research
April 11, 2013
Cited by 393Open Access
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Abstract

RATIONALE: Cardiomyocytes in adult mammalian hearts are terminally differentiated cells that have exited from the cell cycle and lost most of their proliferative capacity. Death of mature cardiomyocytes in pathological cardiac conditions and the lack of regeneration capacity of adult hearts are primary causes of heart failure and mortality. However, how cardiomyocyte proliferation in postnatal and adult hearts becomes suppressed remains largely unknown. The miR-17-92 cluster was initially identified as a human oncogene that promotes cell proliferation. However, its role in the heart remains unknown. OBJECTIVE: To test the hypothesis that miR-17-92 participates in the regulation of cardiomyocyte proliferation in postnatal and adult hearts. METHODS AND RESULTS: We deleted miR-17-92 cluster from embryonic and postnatal mouse hearts and demonstrated that miR-17-92 is required for cardiomyocyte proliferation in the heart. Transgenic overexpression of miR-17-92 in cardiomyocytes is sufficient to induce cardiomyocyte proliferation in embryonic, postnatal, and adult hearts. Moreover, overexpression of miR-17-92 in adult cardiomyocytes protects the heart from myocardial infarction-induced injury. Similarly, we found that members of miR-17-92 cluster, miR-19 in particular, are required for and sufficient to induce cardiomyocyte proliferation in vitro. We identified phosphatase and tensin homolog, a tumor suppressor, as an miR-17-92 target to mediate the function of miR-17-92 in cardiomyocyte proliferation. CONCLUSIONS: Our studies therefore identify miR-17-92 as a critical regulator of cardiomyocyte proliferation, and suggest this cluster of microRNAs could become therapeutic targets for cardiac repair and heart regeneration.


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