Apoptosis role of FAS/FAS ligand system in the regulation of myelopoiesis

Yale J Biol Med. 2005 Jan;78(1):25-36.

Abstract

Objectives: CD34+ cells and colony forming unit-granulocyte and macrophage (CFU-GM) from human bone marrow were used to investigate the role of Fas/FasL system in the regulation of myelopoiesis.

Methods: Fas and FasL expression in CD34+ cells and in day 14 CFU-GM were measured by RT-PCR and immunofluorescence respectively. The functional assays for the CFU-GM were measured by a standard colony assay and the proliferative capacity of CFU-GM was measured by replating the primary colony and observing the secondary colony formation. Human marrow cells were treated with IETD (caspase-8 inhibitor) or anti-Fas CH-11 Mab.

Results: Treatment with the CFU-GM with IETD significantly increased, the proliferative capacity, while anti-Fas CH-11 Mab markedly reduced it. Fas and FasL expression were demonstrated using RT-PCR and immunofluorescence respectively.

Conclusion: Fas, FasL, and caspase activation are likely to play an important role in the regulation of myelopoiesis.

MeSH terms

  • Antigens, CD34 / metabolism*
  • Apoptosis / physiology*
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / metabolism
  • Cell Proliferation
  • Cells, Cultured
  • Fas Ligand Protein
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / metabolism*
  • Homeostasis / physiology
  • Humans
  • Membrane Glycoproteins / metabolism*
  • Myelopoiesis / physiology*
  • Receptors, Tumor Necrosis Factor / metabolism*
  • Tumor Necrosis Factors / metabolism*
  • fas Receptor

Substances

  • Antigens, CD34
  • FAS protein, human
  • FASLG protein, human
  • Fas Ligand Protein
  • Membrane Glycoproteins
  • Receptors, Tumor Necrosis Factor
  • Tumor Necrosis Factors
  • fas Receptor