C-KIT Expression Distinguishes Fetal from Postnatal Skeletal Progenitors

Stem Cell Reports. 2020 Apr 14;14(4):614-630. doi: 10.1016/j.stemcr.2020.03.001. Epub 2020 Mar 26.

Abstract

Hematopoietic stem cells (HSCs) and skeletal stem cells (SSCs) cohabit in the bone marrow. KITL (C-KIT ligand) from LEPR+ adult bone marrow stromal cells is pivotal for HSC maintenance. In contrast, it remains unclear whether KITL/C-KIT signaling also regulates SSCs. Here, we lineage traced C-KIT+ cells and found that C-KIT was expressed by fetal, but not postnatal skeletal progenitors. Fetal C-KIT+ cells gave rise to 20% of LEPR+ stromal cells in adult bone marrow, forming nearly half of all osteoblasts. Disruption of mTOR signaling in fetal C-KIT+ cells impaired bone formation. Notably, conditional deletion of Kitl from PRX1+ fetal bone marrow stromal cells, but not LEPR+ adult bone marrow stromal cells, significantly increased bone formation. Thus, our work identified C-KIT+ skeletal progenitors as an important source of bones formed during development.

Keywords: C-KIT; KITL; SCF; bone; hematopoietic stem cells; skeletal progenitors; skeletal stem cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / metabolism
  • Animals
  • Animals, Newborn
  • Bone Development
  • Bone Marrow Cells / metabolism
  • Bone and Bones / cytology*
  • Cell Lineage
  • Chondrocytes / cytology
  • Chondrocytes / metabolism
  • Fetus / cytology*
  • Gene Deletion
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / metabolism
  • Mice
  • Osteoblasts / cytology
  • Osteoblasts / metabolism
  • Osteogenesis
  • Proto-Oncogene Proteins c-kit / metabolism*
  • Signal Transduction
  • Stem Cell Factor / metabolism
  • Stem Cells / cytology*
  • Transcriptome / genetics

Substances

  • Stem Cell Factor
  • Proto-Oncogene Proteins c-kit