Muscle-specific deletion of rictor impairs insulin-stimulated glucose transport and enhances Basal glycogen synthase activity

Mol Cell Biol. 2008 Jan;28(1):61-70. doi: 10.1128/MCB.01405-07. Epub 2007 Oct 29.

Abstract

Rictor is an essential component of mTOR (mammalian target of rapamycin) complex 2 (mTORC2), a kinase complex that phosphorylates Akt at Ser473 upon activation of phosphatidylinositol 3-kinase (PI-3 kinase). Since little is known about the role of either rictor or mTORC2 in PI-3 kinase-mediated physiological processes in adult animals, we generated muscle-specific rictor knockout mice. Muscle from male rictor knockout mice exhibited decreased insulin-stimulated glucose uptake, and the mice showed glucose intolerance. In muscle lacking rictor, the phosphorylation of Akt at Ser473 was reduced dramatically in response to insulin. Furthermore, insulin-stimulated phosphorylation of the Akt substrate AS160 at Thr642 was reduced in rictor knockout muscle, indicating a defect in insulin signaling to stimulate glucose transport. However, the phosphorylation of Akt at Thr308 was normal and sufficient to mediate the phosphorylation of glycogen synthase kinase 3 (GSK-3). Basal glycogen synthase activity in muscle lacking rictor was increased to that of insulin-stimulated controls. Consistent with this, we observed a decrease in basal levels of phosphorylated glycogen synthase at a GSK-3/protein phosphatase 1 (PP1)-regulated site in rictor knockout muscle. This change in glycogen synthase phosphorylation was associated with an increase in the catalytic activity of glycogen-associated PP1 but not increased GSK-3 inactivation. Thus, rictor in muscle tissue contributes to glucose homeostasis by positively regulating insulin-stimulated glucose uptake and negatively regulating basal glycogen synthase activity.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Biological Transport
  • Carrier Proteins / drug effects
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • GTPase-Activating Proteins / metabolism
  • Gene Expression Regulation*
  • Glucose / metabolism*
  • Glycogen / metabolism
  • Glycogen Synthase / metabolism*
  • Insulin / pharmacology*
  • Male
  • Mice
  • Mice, Knockout
  • Muscles / drug effects*
  • Muscles / metabolism*
  • Phosphorylation / drug effects
  • Phosphoserine / metabolism
  • Phosphothreonine / metabolism
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism
  • Rapamycin-Insensitive Companion of mTOR Protein

Substances

  • Carrier Proteins
  • GTPase-Activating Proteins
  • Insulin
  • Rapamycin-Insensitive Companion of mTOR Protein
  • Tbc1d4 protein, mouse
  • rictor protein, mouse
  • Phosphothreonine
  • Phosphoserine
  • Glycogen
  • Glycogen Synthase
  • Proto-Oncogene Proteins c-akt
  • Glucose