MicroRNA-processing Enzyme Dicer Is Required in Epicardium for Coronary Vasculature Development

被引:38
作者
Singh, Manvendra K. [1 ,2 ]
Lu, Min Min [2 ]
Massera, Daniele [1 ]
Epstein, Jonathan A. [1 ,2 ]
机构
[1] Univ Penn, Dept Cell & Dev Biol, Perelman Sch Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Cardiovasc Inst, Perelman Sch Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
EPITHELIAL-MESENCHYMAL TRANSITIONS; NEURAL CREST; PROGENITOR CELLS; MOUSE DEVELOPMENT; ARTERY FORMATION; CHICK-EMBRYOS; HEART; MUSCLE; DIFFERENTIATION; CARDIOMYOCYTE;
D O I
10.1074/jbc.M111.268573
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The epicardium is a sheet of epithelial cells covering the heart during early cardiac development. In recent years, the epicardium has been identified as an important contributor to cardiovascular development, and epicardium-derived cells have the potential to differentiate into multiple cardiac cell lineages. Some epicardium-derived cells that undergo epithelial-to-mesenchymal transition and delaminate from the surface of the developing heart subsequently invade the myocardium and differentiate into vascular smooth muscle of the developing coronary vasculature. MicroRNAs (miRNAs) have been implicated broadly in tissue patterning and development, including in the heart, but a role in epicardium is unknown. To examine the role of miRNAs during epicardial development, we conditionally deleted the miRNA-processing enzyme Dicer in the proepicardium using Gata5-Cre mice. Epicardial Dicer mutant mice are born in expected Mendelian ratios but die immediately after birth with profound cardiac defects, including impaired coronary vessel development. We found that loss of Dicer leads to impaired epicardial epithelial-to-mesenchymal transition and a reduction in epicardial cell proliferation and differentiation into coronary smooth muscle cells. These results demonstrate a critical role for Dicer, and by implication miRNAs, in murine epicardial development.
引用
收藏
页码:41036 / 41045
页数:10
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