Cell and Tissue Research

, Volume 273, Issue 2, pp 279–286

Evidence for a direct effect of growth hormone on osteoblasts

  • G. Morel
  • P. Chavassieux
  • B. Barenton
  • P. M. Dubois
  • P. J. Meunier
  • G. Boivin
Article

DOI: 10.1007/BF00312829

Cite this article as:
Morel, G., Chavassieux, P., Barenton, B. et al. Cell Tissue Res (1993) 273: 279. doi:10.1007/BF00312829

Abstract

In order to determine whether growth hormone (GH) exerts a direct effect on osteoblasts, in vitro and in vivo immunocytological studies were carried out on newborn rat calvaria and a clonal osteoblast-like cell line (MC3T3-E1) isolated from newborn mouse calvaria. After exposure to human growth hormone (hGH) or 1,25 dihydroxyvitamin D3 (1,25(OH)2D3), a significant increase in alkaline phosphatase activity was observed in MC3T3-E1 cells. Simultaneous exposure of MC3T3-E1 cells to hGH and 10 nM 1,25(OH)2D3 showed a synergistic effect of the two hormones on this activity. The optimal dose of hGH was 0.1 nM. An immunocytological procedure was performed on ultrathin frozen sections from 7-day-old rat calvaria and MC3T3-E1 cells cultured with hGH. GH-like immunoreactivity was observed in both cases. In calvaria, endogenous GH-like immunoreactivity was localized at the same ultrastructural level (plasma membrane, cytoplasmic and nuclear matrices) as exogenous GH-like immunoreactivity in MC3T3-E1 cells. Following the initial step of binding to the plasma membrane, GH may be internalized in the cytoplasmic matrix and nucleus. In situ hybridization revealed the presence of mRNA coding for GH receptor in calvaria cells. The density of these receptors seemed to be lower in osteoblasts than in hepatocytes. In MC3T3-E1 cells, hGH induced a dose-dependent secretion of insulin-like growth factor 1. In conclusion, these results indicate that GH may act directly on osteoblasts.

Key words

Osteoblasts Growth hormone Growth hormone-receptor Alkaline phosphatase Immunocytology Rat (Wistar) 

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Copyright information

© Springer-Verlag 1993

Authors and Affiliations

  • G. Morel
    • 1
  • P. Chavassieux
    • 2
  • B. Barenton
    • 3
  • P. M. Dubois
    • 1
  • P. J. Meunier
    • 2
  • G. Boivin
    • 2
  1. 1.CNRS URA 1454Faculté de Médecine Lyon-SudOullinsFrance
  2. 2.INSERM Unité 234Faculté Alexis CarrelLyonFrance
  3. 3.Physiologie AnimaleINRAMontpellierFrance

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