SCA-1 Expression Level Identifies Quiescent Hematopoietic Stem and Progenitor Cells

Stem Cell Reports. 2017 Jun 6;8(6):1472-1478. doi: 10.1016/j.stemcr.2017.04.012. Epub 2017 May 11.

Abstract

Blood cell generation depends on continuous cellular output by the sequential hierarchy of hematopoietic stem cell (HSC) and progenitor populations that all contain quiescent and actively cycling cells. Hematopoietic stem and progenitor cells (HSPCs) express the surface molecule Stem cell antigen 1 (SCA-1/LY6A). Using histone 2B-red fluorescent fusion protein label retention and cell-cycle reporter mice, we demonstrate that high SCA-1 expression (SCA-1hi) identifies not only quiescent HSCs but quiescent cells on all hierarchical levels within the lineage-SCA-1+KIT+ (LSK) population. Each transplanted SCA-1hi HSPC population also displayed self-renewal potential superior to that of the respective SCA-1lo population. SCA-1 expression is inducible by type I interferon (IFN). We show, however, that quiescence and high self-renewal capacity of cells with brighter SCA-1 expression at steady state were independent of type I IFN signaling. We conclude that SCA-1 expression levels can be used to prospectively isolate functionally heterogeneous HSPC subpopulations.

Keywords: cell cycle; hematopoeitic progenitor cells; hematopoeitic stem cells; hematopoietic stem and progenitor cell heterogeneity; hematopoietic stem and progenitor cell potential; hematopoietic stem and progenitor cell purification and analysis; type I interferon.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Ly / genetics
  • Antigens, Ly / metabolism*
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / metabolism
  • Cell Self Renewal
  • Cells, Cultured
  • Hematopoietic Stem Cell Transplantation
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / metabolism*
  • Histones / genetics
  • Histones / metabolism
  • Interferon Type I / metabolism
  • Ki-67 Antigen / genetics
  • Ki-67 Antigen / metabolism
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Receptor, Interferon alpha-beta / deficiency
  • Receptor, Interferon alpha-beta / genetics
  • Recombinant Fusion Proteins / biosynthesis
  • Recombinant Fusion Proteins / genetics
  • Signal Transduction
  • Transplantation, Homologous

Substances

  • Antigens, Ly
  • Histones
  • Ifnar1 protein, mouse
  • Interferon Type I
  • Ki-67 Antigen
  • Ly6a protein, mouse
  • Membrane Proteins
  • Recombinant Fusion Proteins
  • Receptor, Interferon alpha-beta