Author
Listed:
- Nishat Sultana
(The Black Family Stem Cell Institute, and The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai)
- Lu Zhang
(The Black Family Stem Cell Institute, and The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai)
- Jianyun Yan
(The Black Family Stem Cell Institute, and The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai)
- Jiqiu Chen
(Cardiovascular Research Center, Icahn School of Medicine at Mount Sinai)
- Weibin Cai
(The Black Family Stem Cell Institute, and The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai)
- Shegufta Razzaque
(The Black Family Stem Cell Institute, and The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai)
- Dongtak Jeong
(Cardiovascular Research Center, Icahn School of Medicine at Mount Sinai)
- Wei Sheng
(Cardiovascular Center, Children’s Hospital of Fudan University)
- Lei Bu
(New York University School of Medicine)
- Mingjiang Xu
(Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine)
- Guo-Ying Huang
(Cardiovascular Center, Children’s Hospital of Fudan University)
- Roger J. Hajjar
(Cardiovascular Research Center, Icahn School of Medicine at Mount Sinai)
- Bin Zhou
(Albert Einstein College of Medicine of Yeshiva University)
- Anne Moon
(Weis Center for Research, Geisinger Clinic)
- Chen-Leng Cai
(The Black Family Stem Cell Institute, and The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai)
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.
Suggested Citation
Nishat Sultana & Lu Zhang & Jianyun Yan & Jiqiu Chen & Weibin Cai & Shegufta Razzaque & Dongtak Jeong & Wei Sheng & Lei Bu & Mingjiang Xu & Guo-Ying Huang & Roger J. Hajjar & Bin Zhou & Anne Moon & Ch, 2015.
"Resident c-kit+ cells in the heart are not cardiac stem cells,"
Nature Communications, Nature, vol. 6(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms9701
DOI: 10.1038/ncomms9701
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