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- W2254879660 abstract "Abstract Identifying a bona fide population of cardiac stem cells (CSCs) is a critical step for developing cell-based therapies for heart failure patients. Previously, cardiac c-kit + cells were reported to be CSCs with a potential to become myocardial, endothelial and smooth muscle cells in vitro and after cardiac injury. Here we provide further insights into the nature of cardiac c-kit + cells. By targeting the c-kit locus with multiple reporter genes in mice, we find that c-kit expression rarely co-localizes with the expression of the cardiac progenitor and myogenic marker Nkx2.5 , or that of the myocardial marker, cardiac troponin T (cTnT) . Instead, c-kit predominantly labels a cardiac endothelial cell population in developing and adult hearts. After acute cardiac injury, c-kit + cells retain their endothelial identity and do not become myogenic progenitors or cardiomyocytes. Thus, our work strongly suggests that c-kit + cells in the murine heart are endothelial cells and not CSCs." @default.
- W2254879660 created "2016-06-24" @default.
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- W2254879660 date "2015-10-30" @default.
- W2254879660 modified "2023-09-30" @default.
- W2254879660 title "Resident c-kit+ cells in the heart are not cardiac stem cells" @default.
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- W2254879660 doi "https://doi.org/10.1038/ncomms9701" @default.
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