HLA-DR inhibits granulocytic differentiation without inducing apoptosis of CD34 cells

Hum Immunol. 1999 Oct;60(10):944-54. doi: 10.1016/s0198-8859(99)00089-0.

Abstract

Hematopoietic progenitors express HLA-DR molecules. However the significance of HLA-class II molecules on CD34+ cells remains unknown. The primary role of HLA-class-II molecules is antigen presentation although a second role, that of signal transduction, has been established in B cells. The role of HLA-DR in hematopoiesis was examined by determining the ability of CD34+ progenitor cells to differentiate to "Colony Forming Unit Granulocyte-Macrophage" (CFU-GM) and "Burst Forming Unit Erythrocyte" (BFU-E) in the presence of anti-HLA-DR monoclonal antibody. We observed a reduction in the number of CFU-GM which was due in part to down regulation of granulocyte rather than monocyte differentiation. These observations suggest that HLA-DR signals can regulate myelopoiesis. We point out especially the role of the HLA-DR molecule in the switch of CFU-GM between granulocyte or monocyte lineages. Although HLA-DR mediated apoptosis has been described in mature B lymphocytes apoptosis of CD34+ cells was excluded as a mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / pharmacology
  • Antigens, CD34 / isolation & purification*
  • Apoptosis*
  • Cell Differentiation
  • Colony-Forming Units Assay
  • Fas Ligand Protein
  • Granulocytes / cytology*
  • HLA-DR Antigens / metabolism*
  • Hematopoiesis
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / drug effects
  • Hematopoietic Stem Cells / immunology
  • Humans
  • Lewis X Antigen / isolation & purification
  • Lipopolysaccharide Receptors / isolation & purification
  • Macrophages / cytology
  • Membrane Glycoproteins / immunology
  • Membrane Glycoproteins / metabolism
  • Monocytes / cytology
  • fas Receptor / immunology
  • fas Receptor / metabolism

Substances

  • Antibodies, Monoclonal
  • Antigens, CD34
  • FASLG protein, human
  • Fas Ligand Protein
  • HLA-DR Antigens
  • Lewis X Antigen
  • Lipopolysaccharide Receptors
  • Membrane Glycoproteins
  • fas Receptor