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PMID: 10544260 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Overexpression of the glucose transporter GLUT4 in adipose cells interferes with insulin-stimulated translocation.

FEBS letters ·Vol. 460 ·No. 2 ·1999-10-29 ·Pages 338-42

Al-Hasani H, Yver DR, Cushman SW

Abstract

In adipose cells, insulin induces the translocation of GLUT4 by stimulating their exocytosis from a basal intracellular compartment to the plasma membrane. Increasing overexpression of a hemagglutinin (HA) epitope-tagged GLUT4 in rat adipose cells results in a roughly proportional increase in cell surface HA-GLUT4 levels in the basal state, accompanied by a marked reduction of the fold HA-GLUT4 translocation in response to insulin. Using biochemical methods and cotransfection experiments with differently epitope-tagged GLUT4, we show that overexpression of GLUT4 does not affect the intracellular sequestration of GLUT4 in the absence of insulin, but rather reduces the relative insulin-stimulated GLUT4 translocation to the plasma membrane. In contrast, overexpression of GLUT1 does not interfere with the targeting of GLUT4 and vice versa. These results suggest that the mechanism involved in the intracellular sequestration of GLUT4 has a high capacity whereas the mechanism for GLUT4 translocation is readily saturated by overexpression of GLUT4, implicating an active translocation machinery in the exocytosis of GLUT4.

MeSH Terms
Adipocytes/metabolism Animals Biological Transport/drug effects Blotting, Western Cells, Cultured Dose-Response Relationship, Drug Glucose Transporter Type 4 Hemagglutinins/metabolism Insulin/pharmacology Membrane Proteins/metabolism Monosaccharide Transport Proteins/metabolism Muscle Proteins Plasmids/metabolism Rats Recombinant Fusion Proteins/metabolism Time Factors Transfection
Chemicals
Glucose Transporter Type 4 Hemagglutinins Insulin Membrane Proteins Monosaccharide Transport Proteins Muscle Proteins Recombinant Fusion Proteins Slc2a4 protein, rat
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Al-Hasani H
Experimental Diabetes, Metabolism, and Nutrition Section, National Institutes of Health, Bethesda, MD 20892, USA. [email protected]
Yver D R
Cushman S W
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1999-10-29
Pages
338-42
Language
English
Region
England
NLM ID
0155157
Subset
IM
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