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PMID: 8626583 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Insulin-mediated targeting of phosphatidylinositol 3-kinase to GLUT4-containing vesicles.

The Journal of biological chemistry ·Vol. 271 ·No. 17 ·1996-04-26 ·Pages 10200-4

Heller-Harrison RA, Morin M, Guilherme A, Czech MP

Abstract

Phosphatidylinositol (PI) 3-kinase is hypothesized to be a signaling element in the acute redistribution of intracellular GLUT4 glucose transporters to the plasma membrane in response to insulin. However, some receptors activate PI 3-kinase without causing GLUT4 translocation, suggesting specific cellular localization may be critical to this PI 3-kinase function. Consistent with this idea, complexes containing PI 3-kinase bound to insulin receptor substrate 1 (IRS-1) in 3T3-L1 adipocytes are associated with intracellular membranes (Heller-Harrison, R., Morin, M. and Czech, M. (1995) J. Biol. Chem. 270, 24442-24450). We report here that in response to insulin, activated complexes of IRS-1.PI 3-kinase can be immunoprecipitated with anti-IRS-1 antibody from detergent extracts of immunoadsorbed GLUT4-containing vesicles prepared from 3T3-L1 adipocytes. The targeting of PI 3-kinase to rat adipocyte GLUT4-containing vesicles using vesicles prepared by sucrose velocity gradient ultracentrifugation was also demonstrated. Insulin treatment caused a 2.3-fold increase in immunoreactive p85 protein in these GLUT4-containing vesicles while anti-p85 immunoprecipitates of PI 3-kinase activity in GLUT4-containing vesicle extracts increased to a similar extent. HPLC analysis of the GLUT4 vesicle-associated PI 3-kinase activity showed insulin-mediated increases in PI 3-P, PI 3,4-P2, and PI 3,4,5-P3 when PI, PI 4-P, and PI 4,5-P2 were used as substrates. Our data demonstrate that insulin directs the association of PI 3-kinase with GLUT4-containing vesicles in 3T3-L1 and rat adipocytes, consistent with the hypothesis that PI 3-kinase is involved in the insulin-regulated movement of GLUT4 to the plasma membrane.

MeSH Terms
3T3 Cells Adipocytes/metabolism,ultrastructure Animals Cell Compartmentation/drug effects Enzyme Activation Glucose Transporter Type 4 Insulin/physiology Insulin Receptor Substrate Proteins Mice Monosaccharide Transport Proteins/metabolism Muscle Proteins Organelles/metabolism Phosphatidylinositol 3-Kinases Phosphoproteins/metabolism Phosphotransferases (Alcohol Group Acceptor)/metabolism Rats Receptor, Insulin/physiology Signal Transduction
Chemicals
Glucose Transporter Type 4 Insulin Insulin Receptor Substrate Proteins Irs1 protein, mouse Irs1 protein, rat Monosaccharide Transport Proteins Muscle Proteins Phosphoproteins Slc2a4 protein, mouse Slc2a4 protein, rat Phosphatidylinositol 3-Kinases Phosphotransferases (Alcohol Group Acceptor) Receptor, Insulin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Heller-Harrison R A
Program in Molecular Medicine, University of Massachusetts Medical Center, Worcester, Massachusetts 01605, USA.
Morin M
Guilherme A
Czech M P
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1996-04-26
Pages
10200-4
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIDDK NIH HHS · DK30898 · United States
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