Insulin-like growth factor I stimulates proliferation and Fas-mediated apoptosis of human osteoblasts

Biochem Biophys Res Commun. 1998 Jun 9;247(1):46-51. doi: 10.1006/bbrc.1998.8728.

Abstract

In vitro studies have shown that insulin-like growth factor I (IGF-I) is a potent growth factor for osteoblasts, although both bone formation and resorption are upregulated by IGF-I in vivo. To understand the difference in the action of IGF-I observed in vitro and in vivo experiments, we examined the effect of IGF-I on the proliferation and Fas-mediated apoptosis of human osteoblasts in vitro. Human osteoblastic cell line MG63 and human primary osteoblast-like cells obtained from biopsy specimens were used as human osteoblasts. Cells were cultured with or without various concentrations of IGF-I followed by determination of the proliferative response and Fas-mediated apoptosis. IGF-I dose dependently stimulated the proliferation of cultured human osteoblasts. Both Fas expression and the degree of anti-Fas IgM-induced apoptosis of human osteoblasts was also augmented by IGF-I. Furthermore, the cytotoxicity of Fas ligand (FasL) cDNA transformants against human osteoblasts was increased when IGF-I-stimulated osteoblasts were used as target cells, indicating that stimulation of IGF-I increased functional Fas expression on human osteoblasts as well as their proliferation. The addition of DEVD-CHO, a specific inhibitor of CPP32, to the culture resulted in a significant inhibition of Fas-mediated apoptosis of both unstimulated and IGF-I-stimulated osteoblasts, although it did not affect the proliferative response or Fas expression. Our data suggest that activation of CPP32 is necessary for Fas-mediated apoptosis of human osteoblasts, and treatment of IGF-I increased this signaling pathway. In contrast, regulation of proliferation and Fas expression of the cells were probably not affected by CPP32 activation. Our results suggest that IGF-I acts on cultured human osteoblasts by increasing their proliferation and induction of Fas-mediated apoptosis by neighbouring FasL+ cells such as osteoclasts, thus probably functioning as a local coupling factor in the bone in vivo, stimulating both bone formation and resorption.

MeSH terms

  • Apoptosis / drug effects*
  • Apoptosis / genetics
  • Apoptosis / immunology
  • Cell Division / drug effects
  • Cell Line
  • Cells, Cultured
  • Cytotoxicity Tests, Immunologic
  • Fas Ligand Protein
  • Humans
  • Insulin-Like Growth Factor I / pharmacology*
  • Leukemia, Erythroblastic, Acute
  • Ligands
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / toxicity
  • Oligopeptides / pharmacology
  • Osteoblasts / cytology*
  • Osteoblasts / immunology
  • Osteoblasts / metabolism
  • Tumor Cells, Cultured
  • fas Receptor / drug effects
  • fas Receptor / genetics
  • fas Receptor / physiology*

Substances

  • FASLG protein, human
  • Fas Ligand Protein
  • Ligands
  • Membrane Glycoproteins
  • Oligopeptides
  • aspartyl-glutamyl-valyl-aspartal
  • fas Receptor
  • Insulin-Like Growth Factor I