Epidermal growth factor triggers the translocation of insulin-responsive glucose transporter (GLUT4)

Biochem Biophys Res Commun. 1994 Nov 30;205(1):857-63. doi: 10.1006/bbrc.1994.2743.

Abstract

In a novel cell line we developed for direct, sensitive detection of insulin-responsive glucose transporter (GLUT4) on the cell surface, we considered that insulin-activated phosphatidylinositol 3-kinase (PI 3-kinase) may be involved in the signaling pathway of insulin-stimulated GLUT4 translocation. We report here evidence that epidermal growth factor (EGF), which stimulates PI 3-kinase activity, also triggers GLUT4 translocation in Chinese hamster ovary (CHO) cells stably overexpressing the EGF receptor. The EGF-dependent GLUT4 translocation is possibly mediated by two independent pathways: one by PI 3-kinase and the other by protein kinase C (PKC); the PI 3-kinase-mediated pathway predominates. Triggering of the GLUT4 translocation is not specific for insulin, rather it may be a common property of growth factors which activate PI 3-kinase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Androstadienes / pharmacology
  • Animals
  • Biological Transport
  • CHO Cells
  • Cricetinae
  • Enzyme Activation
  • Epidermal Growth Factor / physiology*
  • Glucose / metabolism
  • Glucose Transporter Type 4
  • Insulin / pharmacology*
  • Monosaccharide Transport Proteins / metabolism*
  • Muscle Proteins*
  • Phorbol 12,13-Dibutyrate / pharmacology
  • Phosphatidylinositol 3-Kinases
  • Phosphotransferases (Alcohol Group Acceptor) / antagonists & inhibitors
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism
  • Wortmannin

Substances

  • Androstadienes
  • Glucose Transporter Type 4
  • Insulin
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • Phorbol 12,13-Dibutyrate
  • Epidermal Growth Factor
  • Phosphatidylinositol 3-Kinases
  • Phosphotransferases (Alcohol Group Acceptor)
  • Glucose
  • Wortmannin