The inhibition of glycogen synthase kinase-3 by insulin or insulin-like growth factor 1 in the rat skeletal muscle cell line L6 is blocked by wortmannin, but not by rapamycin: evidence that wortmannin blocks activation of the mitogen-activated protein kinase pathway in L6 cells between Ras and Raf

Biochem J. 1994 Oct 1;303 ( Pt 1)(Pt 1):21-6. doi: 10.1042/bj3030021.

Abstract

Glycogen synthase kinase-3 (GSK3) is inactivated in vitro by p70 S6 kinase or MAP kinase-activated protein kinase-1 beta (MAPKAP kinase-1 beta; also known as Rsk-2). Here we show that GSK3 isoforms are inhibited by 40% within minutes after stimulation of the rat skeletal-muscle cell line L6 with insulin-like growth factor-1 (IGF-1) or insulin. GSK3 was similarly inhibited in rabbit skeletal muscle after an intravenous injection of insulin. Inhibition resulted from increased phosphorylation of GSK3, probably at a serine/threonine residue(s), because it was reversed by incubation with protein phosphatase-2A. Rapamycin blocked the activation of p70 S6 kinase by IGF-1 in L6 cells, but had no effect on the inhibition of GSK3 or the activation of MAPKAP kinase-1 beta. In contrast, wortmannin, a potent inhibitor of PtdIns 3-kinase, prevented the inactivation of GSK3 and the activation of MAPKAP kinase-1 beta and p70 S6 kinase by IGF-1 or insulin. Wortmannin also blocked the activation of p74raf-1. MAP kinase kinase and p42 MAP kinase, but not the formation of GTP-Ras by IGF-1. The results suggest that the stimulation of glycogen synthase by insulin/IGF-1 in skeletal muscle involves the MAP-KAP kinase-1-catalysed inhibition of GSK3, as well as the previously described activation of the glycogen-associated form of protein phosphatase-1.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Androstadienes / pharmacology*
  • Animals
  • Antibodies
  • Calcium-Calmodulin-Dependent Protein Kinases / antagonists & inhibitors*
  • Cell Line
  • Enzyme Activation
  • Female
  • Glycogen Synthase / metabolism
  • Glycogen Synthase Kinase 3
  • Glycogen Synthase Kinases
  • Immunosuppressive Agents / pharmacology
  • Insulin / pharmacology*
  • Insulin-Like Growth Factor I / pharmacology*
  • Kinetics
  • Molecular Sequence Data
  • Muscles / enzymology*
  • Peptides / chemical synthesis
  • Peptides / immunology
  • Polyenes / pharmacology*
  • Protein Serine-Threonine Kinases / metabolism*
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-raf
  • Rabbits
  • Rats
  • Sirolimus
  • Wortmannin
  • ras Proteins / metabolism*

Substances

  • Androstadienes
  • Antibodies
  • Immunosuppressive Agents
  • Insulin
  • Peptides
  • Polyenes
  • Proto-Oncogene Proteins
  • Insulin-Like Growth Factor I
  • Glycogen Synthase
  • Glycogen Synthase Kinases
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-raf
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Glycogen Synthase Kinase 3
  • ras Proteins
  • Sirolimus
  • Wortmannin