Epicardial progenitors contribute to the cardiomyocyte lineage in the developing heart

被引:758
作者
Zhou, Bin [1 ,2 ,3 ]
Ma, Qing [1 ,2 ,3 ]
Rajagopal, Satish [1 ,2 ,3 ]
Wu, Sean M. [4 ,5 ]
Domian, Ibrahim [4 ,5 ]
Rivera-Feliciano, Jose [3 ]
Jiang, Dawei [1 ,2 ]
von Gise, Alexander [1 ,2 ,3 ,6 ]
Ikeda, Sadakatsu [1 ,2 ,3 ]
Chien, Kenneth R. [4 ,5 ]
Pu, William T. [1 ,2 ,3 ]
机构
[1] Childrens Hosp, Harvard Stem Cell Inst, Boston, MA 02115 USA
[2] Childrens Hosp, Dept Cardiol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[4] Harvard Univ, Harvard Stem Cell Inst, Boston, MA 02114 USA
[5] Massachusetts Gen Hosp, Cardiovasc Res Ctr, Boston, MA 02114 USA
[6] Charite Univ Med Berlin, Clin Neonatol, D-10117 Berlin, Germany
关键词
D O I
10.1038/nature07060
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The heart is formed from cardiogenic progenitors expressing the transcription factors Nkx2-5 and Isl1 ( refs 1 and 2). These multipotent progenitors give rise to cardiomyocyte, smooth muscle and endothelial cells, the major lineages of the mature heart(3,4). Here we identify a novel cardiogenic precursor marked by expression of the transcription factor Wt1 and located within the epicardium - an epithelial sheet overlying the heart. During normal murine heart development, a subset of these Wt1(+) precursors differentiated into fully functional cardiomyocytes. Wt1(+) proepicardial cells arose from progenitors that express Nkx2-5 and Isl1, suggesting that they share a developmental origin with multipotent Nkx2-5(+) and Isl1(+) progenitors. These results identify Wt1(+) epicardial cells as previously unrecognized cardiomyocyte progenitors, and lay the foundation for future efforts to harness the cardiogenic potential of these progenitors for cardiac regeneration and repair.
引用
收藏
页码:109 / U5
页数:6
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