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

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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    Cited by:

    1. Georges Makhoul & Kashif Khan & Renzo Cecere & Bin Yu & Adel Schwertani, 2019. "Triggered Cardiogenesis in Wingless 5a Treated Amniotic Mesenchymal Stromal Cells," Biomedical Journal of Scientific & Technical Research, Biomedical Research Network+, LLC, vol. 16(4), pages 12205-12213, April.

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