4.7 Article

KIT signaling is dispensable for human mast cell progenitor development

Journal

BLOOD
Volume 130, Issue 16, Pages 1785-1794

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2017-03-773374

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Funding

  1. Swedish Research Council
  2. Swedish Cancer Society
  3. Cancer and Allergy Foundation
  4. Stockholm Cancer Society (Radiumhemmets Forskningsfonder)
  5. Tore Nilson's Foundation for Medical Research
  6. Ollie and Elof Ericsson Foundation
  7. Hans von Kantzow's Foundation
  8. Karolinska Institutet

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Human hematopoietic progenitors are generally assumed to require stem cell factor (SCF) and KIT signaling during differentiation for the formation of mast cells. Imatinib treatment, which inhibits KIT signaling, depletes mast cells in vivo. Furthermore, the absence of SCF or imatinib treatment prevents progenitors from developing into mast cells in vitro. However, these observations do not mean that mast cell progenitors require SCF and KIT signaling throughout differentiation. Here, we demonstrate that circulating mast cell progenitors are present in patients undergoing imatinib treatment. In addition, we show that mast cell progenitors from peripheral blood survive, mature, and proliferate without SCF and KIT signaling in vitro. Contrary to the prevailing consensus, our results show that SCF and KIT signaling are dispensable for early mast cell development.

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