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The Role of the Epicardium During Heart Development and Repair

期刊

CIRCULATION RESEARCH
卷 126, 期 3, 页码 377-394

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCRESAHA.119.315857

关键词

fibrosis; growth and development; myocardial ischemia; paracrine communication; regeneration

资金

  1. NIH [T32HL066988, F32HL134206, T32GM068411, R01-HL133761, R01-HL136179, R01-HL120919, R01-HL144867, UL1-TR002001]
  2. American Heart Association [19CDA34590003, 16PRE3049000]
  3. Howard Hughes Medical Institute Med-Into-Grad program
  4. [T32HL07572]
  5. [NYSTEM-C32566GG]

向作者/读者索取更多资源

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.

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