Use of RNA interference-mediated gene silencing and adenoviral overexpression to elucidate the roles of AKT/protein kinase B isoforms in insulin actions

J Biol Chem. 2003 Jul 25;278(30):28312-23. doi: 10.1074/jbc.M302094200. Epub 2003 May 6.

Abstract

Insulin plays a central role in the regulation of glucose homeostasis in part by stimulating glucose uptake and glycogen synthesis. The serine/threonine protein kinase Akt has been proposed to mediate insulin signaling in several processes. However, it is unclear whether Akt is involved in insulin-stimulated glucose uptake and which isoforms of Akt are responsible for each insulin action. We confirmed that expression of a constitutively active Akt, using an adenoviral expression vector, promoted translocation of glucose transporter 4 (GLUT4) to plasma membrane, 2-deoxyglucose (2-DG) uptake, and glycogen synthesis in both Chinese hamster ovary cells and 3T3-L1 adipocytes. Inhibition of Akt either by adenoviral expression of a dominant negative Akt or by the introduction of synthetic 21-mer short interference RNA against Akt markedly reduced insulin-stimulated GLUT4 translocation, 2-DG uptake, and glycogen synthesis. Experiments with isoform-specific short interference RNA revealed that Akt2, and Akt1 to a lesser extent, has an essential role in insulin-stimulated GLUT4 translocation and 2-DG uptake in both cell lines, whereas Akt1 and Akt2 contribute equally to insulin-stimulated glycogen synthesis. These data suggest a prerequisite role of Akt in insulin-stimulated glucose uptake and distinct functions among Akt isoforms.

Publication types

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

MeSH terms

  • 3T3 Cells
  • Adenoviridae / genetics*
  • Animals
  • Base Sequence
  • Brain / metabolism
  • CHO Cells
  • COS Cells
  • Cricetinae
  • Deoxyglucose / pharmacokinetics
  • Dose-Response Relationship, Drug
  • Gene Library
  • Gene Silencing*
  • Genetic Techniques*
  • Glucose Transporter Type 4
  • Glycogen / metabolism
  • Immunoblotting
  • Insulin / metabolism*
  • Luciferases / metabolism
  • Mice
  • Molecular Sequence Data
  • Monosaccharide Transport Proteins / metabolism
  • Muscle Proteins*
  • Plasmids / metabolism
  • Precipitin Tests
  • Protein Isoforms
  • Protein Serine-Threonine Kinases*
  • Protein Transport
  • Proto-Oncogene Proteins / chemistry*
  • Proto-Oncogene Proteins c-akt
  • RNA Interference*
  • Rats
  • Time Factors

Substances

  • Glucose Transporter Type 4
  • Insulin
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • Protein Isoforms
  • Proto-Oncogene Proteins
  • Slc2a4 protein, mouse
  • Slc2a4 protein, rat
  • Glycogen
  • Deoxyglucose
  • Luciferases
  • Akt1 protein, rat
  • Akt2 protein, mouse
  • Akt2 protein, rat
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt