Stimulation of IRS-1-associated phosphatidylinositol 3-kinase and Akt/protein kinase B but not glucose transport by beta1-integrin signaling in rat adipocytes

J Biol Chem. 1998 Dec 11;273(50):33119-22. doi: 10.1074/jbc.273.50.33119.

Abstract

The signal transduction pathway by which insulin stimulates glucose transport is not understood, but a role for complexes of insulin receptor substrate (IRS) proteins and phosphatidylinositol (PI) 3-kinase as well as for Akt/protein kinase B (PKB) has been proposed. Here, we present evidence suggesting that formation of IRS-1/PI 3-kinase complexes and Akt/PKB activation are insufficient to stimulate glucose transport in rat adipocytes. Cross-linking of beta1-integrin on the surface of rat adipocytes by anti-beta1-integrin antibody and fibronectin was found to cause greater IRS-1 tyrosine phosphorylation, IRS-1-associated PI 3-kinase activity, and Akt/PKB activation, detected by anti-serine 473 antibody, than did 1 nM insulin. Clustering of beta1-integrin also significantly potentiated stimulation of insulin receptor and IRS-1 tyrosine phosphorylation, IRS-associated PI 3-kinase activity, and Akt/PKB activation caused by submaximal concentrations of insulin. In contrast, beta1-integrin clustering caused neither a change in deoxyglucose transport nor an effect on the ability of insulin to stimulate deoxyglucose uptake at any concentration along the entire dose-response relationship range. The data suggest that (i) beta1-integrins can engage tyrosine kinase signaling pathways in isolated fat cells, potentially regulating fat cell functions and (ii) either formation of IRS-1/PI 3-kinase complexes and Akt/PKB activation is not necessary for regulation of glucose transport in fat cells or an additional signaling pathway is required.

Publication types

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

MeSH terms

  • Adipocytes / metabolism
  • Animals
  • Biological Transport
  • Enzyme Activation
  • Glucose / metabolism*
  • Insulin Receptor Substrate Proteins
  • Integrin beta1 / metabolism*
  • Male
  • Oncogene Protein v-akt
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphoproteins / metabolism*
  • Phosphorylation
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Insulin / metabolism
  • Retroviridae Proteins, Oncogenic / metabolism*
  • Signal Transduction*
  • Tyrosine / metabolism

Substances

  • Insulin Receptor Substrate Proteins
  • Integrin beta1
  • Irs1 protein, rat
  • Phosphoproteins
  • Retroviridae Proteins, Oncogenic
  • Tyrosine
  • Phosphatidylinositol 3-Kinases
  • Receptor, Insulin
  • Oncogene Protein v-akt
  • Glucose