Differentiation of fetal hematopoietic stem cells requires ARID4B to restrict autocrine KITLG/KIT-Src signaling

Cell Rep. 2021 Nov 23;37(8):110036. doi: 10.1016/j.celrep.2021.110036.

Abstract

Balance between the hematopoietic stem cell (HSC) duality to either possess self-renewal capacity or differentiate into multipotency progenitors (MPPs) is crucial for maintaining homeostasis of the hematopoietic stem/progenitor cell (HSPC) compartment. To retain the HSC self-renewal activity, KIT, a receptor tyrosine kinase, in HSCs is activated by its cognate ligand KITLG originating from niche cells. Here, we show that AT-rich interaction domain 4B (ARID4B) interferes with KITLG/KIT signaling, consequently allowing HSC differentiation. Conditional Arid4b knockout in mouse hematopoietic cells blocks fetal HSC differentiation, preventing hematopoiesis. Mechanistically, ARID4B-deficient HSCs self-express KITLG and overexpress KIT. As to downstream pathways of KITLG/KIT signaling, inhibition of Src family kinases rescues the HSC differentiation defect elicited by ARID4B loss. In summary, the intrinsic ARID4B-KITLG/KIT-Src axis is an HSPC regulatory program that enables the differentiation state, while KIT stimulation by KITLG from niche cells preserves the HSPC undifferentiated pool.

Keywords: ARID4B, HSPC, HSC, MPP, KIT, KITLG.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autocrine Communication
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology
  • Cell Proliferation / physiology
  • Cell Self Renewal / physiology
  • DNA-Binding Proteins / metabolism*
  • DNA-Binding Proteins / physiology
  • Female
  • Hematopoiesis / physiology
  • Hematopoietic Stem Cells / metabolism*
  • Hematopoietic Stem Cells / physiology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Proto-Oncogene Proteins c-kit / genetics
  • Proto-Oncogene Proteins c-kit / metabolism*
  • Signal Transduction / physiology
  • Stem Cell Factor / metabolism
  • Stem Cell Niche / physiology
  • Transcription Factors / metabolism
  • src-Family Kinases / metabolism

Substances

  • DNA-Binding Proteins
  • Kit protein, mouse
  • Rbbp1l1 protein, mouse
  • Stem Cell Factor
  • Transcription Factors
  • Proto-Oncogene Proteins c-kit
  • src-Family Kinases