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

Authors
Sultana, NishatZhang, LuYan, JianyunChen, JiqiuCai, WeibinRazzaque, SheguftaJeong, DongtakSheng, WeiBu, LeiXu, MingjiangHuang, Guo-YingHajjar, Roger J.Zhou, BinMoon, AnneCai, Chen-Leng
Issue Date
Oct-2015
Publisher
NATURE PUBLISHING GROUP
Citation
NATURE COMMUNICATIONS, v.6, pp.1 - 10
Indexed
SCIE
SCOPUS
Journal Title
NATURE COMMUNICATIONS
Volume
6
Start Page
1
End Page
10
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/17006
DOI
10.1038/ncomms9701
ISSN
2041-1723
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.
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COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY > ERICA 의약생명과학과 > 1. Journal Articles

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ERICA 과학기술융합대학 (ERICA 의약생명과학과)
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