Excessive insulin receptor serine phosphorylation in cultured fibroblasts and in skeletal muscle. A potential mechanism for insulin resistance in the polycystic ovary syndrome

J Clin Invest. 1995 Aug;96(2):801-10. doi: 10.1172/JCI118126.

Abstract

We investigated the cellular mechanisms of the unique disorder of insulin action found in the polycystic ovary syndrome (PCOS). Approximately 50% of PCOS women (PCOS-Ser) had a significant increase in insulin-independent beta-subunit [32P]phosphate incorporation (3.7-fold, P < 0.05 vs other groups) in skin fibroblast insulin receptors that was present in serine residues while insulin-induced tyrosine phosphorylation was decreased (both P < 0.05 vs other groups). PCOS skeletal muscle insulin receptors had the same abnormal phosphorylation pattern. The remaining PCOS women (PCOS-n1) had basal and insulin-stimulated receptor autophosphorylation similar to control. Phosphorylation of the artificial substrate poly GLU4:TYR1 by the PCOS-Ser insulin receptors was significantly decreased (P < 0.05) compared to control and PCOS-n1 receptors. The factor responsible for excessive serine phosphorylation appeared to be extrinsic to the receptor since no insulin receptor gene mutations were identified, immunoprecipitation before autophosphorylation corrected the phosphorylation defect and control insulin receptors mixed with lectin eluates from affected PCOS fibroblasts displayed increased serine phosphorylation. Our findings suggest that increased insulin receptor serine phosphorylation decreases its protein tyrosine kinase activity and is one mechanism for the post-binding defect in insulin action characteristic of PCOS.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Blood Glucose / analysis
  • Cells, Cultured
  • Diabetes Mellitus, Type 2 / etiology
  • Female
  • Fibroblasts / metabolism*
  • Humans
  • Insulin / blood
  • Insulin Resistance / physiology*
  • Intercellular Signaling Peptides and Proteins
  • Muscle, Skeletal / metabolism*
  • Muscle, Skeletal / pathology
  • Obesity / etiology
  • Peptides / metabolism
  • Phosphorylation
  • Phosphoserine / metabolism*
  • Polycystic Ovary Syndrome / complications
  • Polycystic Ovary Syndrome / genetics
  • Polycystic Ovary Syndrome / physiopathology*
  • Protein Processing, Post-Translational*
  • Protein-Serine-Threonine Kinases / genetics
  • Protein-Serine-Threonine Kinases / metabolism*
  • Receptor, Insulin / metabolism*
  • Skin / pathology

Substances

  • Blood Glucose
  • Insulin
  • Intercellular Signaling Peptides and Proteins
  • Peptides
  • Phosphoserine
  • L-glutamic acid-L-tyrosine copolymer
  • Receptor, Insulin
  • Protein-Serine-Threonine Kinases