Open AccessEpicardium‐derived cells (EPDCs) in development, cardiac disease and repair of ischemia
Author(s) -
Groot Adriana C. Gittenbergerde,
Winter Elisabeth M.,
Poelmann Robert E.
Publication year - 2010
Publication title -
journal of cellular and molecular medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.44
H-Index - 130
eISSN - 1582-4934
pISSN - 1582-1838
DOI - 10.1111/j.1582-4934.2010.01077.x
Subject(s) - embryonic stem cell , biology , mesenchymal stem cell , ischemia , myocyte , angiogenesis , stem cell , progenitor cell , microbiology and biotechnology , regeneration (biology) , anatomy , pathology , cardiology , cancer research , medicine , genetics , gene
• Development of the epicardium • Epithelial–mesenchymal transition into EPDCs • Derivatives of EPDCs • Potential role of EPDCs in cardiomyopathy and valve disease • Potential of EPDCs as adult stem cells • Reactivation of endogenous epicardium after ischemiaThe proepicardial‐derived epicardium covers the myocardium and after a process of epithelial–mesenchymal transition (EMT) forms epicardium‐derived cells (EPDCs). These cells migrate into the myocardium and show an essential role in the induction of the ventricular compact myocardium and the differentiation of the Purkinje fibres. EPDCs are furthermore the source of the interstitial fibroblast, the coronary smooth muscle cell and the adventitial fibroblast. The possible differentiation into cardiomyocytes, endothelial cells and the recently described telocyte and other cells in the cardiac stem cell niche needs further investigation. Surgically or genetically disturbed epicardial and EPDC differentiation leads to a spectrum of abnormalities varying from thin undifferentiated myocardium, which can be embryonic lethal, to a diminished coronary vascular bed with even absent main coronary arteries. The embryonic potential of EPDCs has been translated to both structural and functional congenital malformations and adult cardiac disease, like development of Ebstein’s malformation, arrhythmia and cardiomyopathies. Furthermore, the use of adult EPDCs as a stem cell source has been explored, showing in an animal model of myocardial ischemia the recapitulation of the embryonic program with improved function, angiogenesis and less adverse remodeling. Combining EPDCs and adult cardiomyocyte progenitor cells synergistically improved these results. The contribution of injected EPDCs was instructive rather than constructive. The finding of reactivation of the endogenous epicardium in ischemia with re‐expression of developmental genes and renewed EMT marks the onset of a novel therapeutic focus.