Functional importance of heat shock protein 90 associated with insulin receptor on insulin-stimulated mitogenesis

Biochem Biophys Res Commun. 1997 Aug 18;237(2):345-7. doi: 10.1006/bbrc.1997.7116.

Abstract

The role of stress proteins on the function of insulin receptor is not well understood. In the rat-1 fibroblasts overexpressing human insulin receptors, heat shock protein (Hsp) 90 was co-immunoprecipitated with insulin receptors and the association was not affected by insulin stimulation. A GST-fusion protein containing the intracellular insulin receptor beta subunit was associated with Hsp 90 in vitro, suggesting the direct interaction of this protein with insulin receptor beta-subunit. Furthermore, microinjection of anti-Hsp 90 antibody into these cells completely inhibited insulin-stimulated mitogenesis. However, neither epidermal growth factor-stimulated nor serum-stimulated mitogenic signal in the cells was affected by the antibody microinjection. These results suggest that Hsp 90 constitutively binds to insulin receptor beta-subunit, which may be necessary for insulin signaling in mitogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carrier Proteins / immunology
  • Carrier Proteins / metabolism
  • Cell Line
  • HSC70 Heat-Shock Proteins
  • HSP70 Heat-Shock Proteins*
  • HSP90 Heat-Shock Proteins / immunology
  • HSP90 Heat-Shock Proteins / metabolism*
  • Humans
  • Insulin / pharmacology*
  • Microinjections
  • Mitogens / pharmacology*
  • Precipitin Tests
  • Protein Binding
  • Rats
  • Receptor, Insulin / metabolism*
  • Signal Transduction

Substances

  • Carrier Proteins
  • HSC70 Heat-Shock Proteins
  • HSP70 Heat-Shock Proteins
  • HSP90 Heat-Shock Proteins
  • HSPA8 protein, human
  • Hspa8 protein, rat
  • Insulin
  • Mitogens
  • Receptor, Insulin