生物
旁分泌信号
间充质干细胞
细胞生物学
再生(生物学)
祖细胞
胚胎干细胞
心脏发育
动脉发生
人口
干细胞
血管生成
癌症研究
医学
遗传学
基因
受体
环境卫生
作者
Pearl Quijada,Michael A. Trembley,Eric M. Small
出处
期刊:Circulation Research
[Ovid Technologies (Wolters Kluwer)]
日期:2020-01-30
卷期号:126 (3): 377-394
被引量:181
标识
DOI:10.1161/circresaha.119.315857
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI