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Resident c-kit(+) cells in the heart are not cardiac stem cells

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...

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Detalles Bibliográficos
Autores principales: Sultana, Nishat, Zhang, Lu, Yan, Jianyun, Chen, Jiqiu, Cai, Weibin, Razzaque, Shegufta, Jeong, Dongtak, Sheng, Wei, Bu, Lei, Xu, Mingjiang, Huang, Guo-Ying, Hajjar, Roger J., Zhou, Bin, Moon, Anne, Cai, Chen-Leng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4846318/
https://www.ncbi.nlm.nih.gov/pubmed/26515110
http://dx.doi.org/10.1038/ncomms9701
Descripción
Sumario: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.