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. Author manuscript; available in PMC: 2015 Apr 15.
Published in final edited form as: Int J Cardiol. 2014 Feb 20;173(1):1–11. doi: 10.1016/j.ijcard.2014.02.008

Table 3.

mi-RNAs involved in cardiac regeneration

micro-RNA Functions Reference
miR-1 Increases differentiation of hPSCs into cardiomyocytes and enhances direct reprogramming of human fibroblasts into cardiomyocytes [89, 91, 92, 148]
miR-499 Overexpression enhances hPSC cardiac differentiation and CPC cardiac differentiation [89, 92]
miR-199a Expression in cardiomyocytes induces proliferation and facilitates cardiac regeration following myocardial infarction in adult mice [82]
miR-15 family Inhibition of this microRNA enhances cardiomyocyte survival following ischemia-reperfusion injury in vitro and in vivo, as well as in response to palmitate in vitro; inhibition also facilitates cardiac regeration following myocardial infarction in adult mice [83, 149152]
miR-199b In vivo inhibition of miR-199b normalized significantly attenuated cardiac functional impairment, fibrosis and NFAT activity; the target of miR-199b is Dyrk1 [153]
mir-29 miR-29 downregulation prenvents aortic dialation [154]
miR-21 Antagomir-21 decreased the development of cardiac fibrosis and improved cardiac function [155157]
miR-98 Overexpression of miR-98 reduced AngII mediated fibrosis and amount of apoptotic myocytes [158]
miR-17-92 cluster Overexpression enhances cardiac progenitor cell proliferation and facilitates cardiac regeneration following myocardial MI in adult mice [90]
miR-23, miR-24 Overexpression Enhances cardiomyocyte survival following MI n in adult mice and enhances angiogenesis [159, 160]
mir-27 Enhances angiogenesis [160]
miR-34a Expression levels gradually increase with age in mice and humans and inihibition enhances cardiomyocyte survival following MI in adult mice [154]
miR-92a, miR-133 Enhances mesodermal differentiation of hPSCs and enhances direct reprogramming of human fibroblasts into cardiomyocytes; [91, 121, 148]
miR-143/145 Knockdown prevents cardiogenesis in murine embryonic stem cell differentiation [161]
miR-378 Inhibition of this microRNA improves cardiomyocyte survival in an in vitro model of hypoxia-reperfusion [162]
miR-590 Expression of this microRNA in cardiomyocytes induces proliferation and facilitates cardiac regeration following MI in adult mice [82]