From the Aab Cardiovascular Research Institute (P.Q., E.M.S.), University of Rochester, School of Medicine and Dentistry, Rochester, NY.
Department of Medicine (P.Q., E.M.S.), University of Rochester, School of Medicine and Dentistry, Rochester, NY.
Circ Res. 2020 Jan 31;126(3):377-394. doi: 10.1161/CIRCRESAHA.119.315857. Epub 2020 Jan 30.
The heart is lined by a single layer of mesothelial cells called the epicardium that provides important cellular contributions for embryonic heart formation. The epicardium harbors a population of progenitor cells that undergo epithelial-to-mesenchymal transition displaying characteristic conversion of planar epithelial cells into multipolar and invasive mesenchymal cells before differentiating into nonmyocyte cardiac lineages, such as vascular smooth muscle cells, pericytes, and fibroblasts. The epicardium is also a source of paracrine cues that are essential for fetal cardiac growth, coronary vessel patterning, and regenerative heart repair. Although the epicardium becomes dormant after birth, cardiac injury reactivates developmental gene programs that stimulate epithelial-to-mesenchymal transition; however, it is not clear how the epicardium contributes to disease progression or repair in the adult. In this review, we will summarize the molecular mechanisms that control epicardium-derived progenitor cell migration, and the functional contributions of the epicardium to heart formation and cardiomyopathy. Future perspectives will be presented to highlight emerging therapeutic strategies aimed at harnessing the regenerative potential of the fetal epicardium for cardiac repair.
心脏由单层间皮细胞(称为心外膜)构成,心外膜为胚胎心脏形成提供了重要的细胞贡献。心外膜包含一群祖细胞,这些细胞经历上皮-间充质转化,表现出平面上皮细胞向多极和侵袭性间充质细胞的特征性转化,然后分化为非心肌细胞谱系,如血管平滑肌细胞、周细胞和成纤维细胞。心外膜也是旁分泌信号的来源,这些信号对胎儿心脏生长、冠状血管模式形成和心脏再生修复至关重要。尽管心外膜在出生后进入休眠状态,但心脏损伤会重新激活发育基因程序,刺激上皮-间充质转化;然而,目前尚不清楚心外膜如何促进成人疾病的进展或修复。在这篇综述中,我们将总结控制心外膜衍生祖细胞迁移的分子机制,以及心外膜对心脏形成和心肌病的功能贡献。未来的展望将突出新兴的治疗策略,旨在利用胎儿心外膜的再生潜力进行心脏修复。