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PMID: 2479643 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The acquisition of increased insulin-responsive hexose transport in 3T3-L1 adipocytes correlates with expression of a novel transporter gene.

The Journal of biological chemistry ·Vol. 264 ·No. 33 ·1989-11-25 ·Pages 19994-9

Garcia de Herreros A, Birnbaum MJ

Abstract

The expression of two genes encoding facilitated glucose transporter proteins was studied during the differentiation of the 3T3-L1 fibroblastic cell line into adipocytes. The mRNA encoding the widely expressed HepG2/brain glucose transporter (GTI) is detectable in fibroblasts and its abundance remains unchanged during differentiation. On the other hand, the mRNA encoding a glucose transporter protein (GTIII) localized exclusively to muscle and adipose tissue is undetectable in fibroblasts but present in adipocytes. GTIII mRNA is first expressed three days after differentiation of 3T3-L1 cells has begun. Similarly, it is not until 3 days following the initiation of differentiation that GTIII protein can be detected, as assayed either by Western immunoblot or indirect immunofluorescence. The latter technique localizes GTIII predominantly to the perinuclear region of the adipocyte. The appearance of GTIII in developing fat cells correlates temporally with the acquisition of an increased stimulation of hexose uptake by maximal concentrations of insulin. These data support the concept that the marked increase in hexose transport in adipocytes in response to insulin is dependent on the expression in these cells of a specific, hormone-regulatable transport protein.

MeSH Terms
Adipose Tissue/drug effects,metabolism Animals Biological Transport, Active/drug effects Blotting, Western Cells, Cultured Deoxy Sugars/metabolism Deoxyglucose/metabolism Gene Expression/drug effects Genes/drug effects Insulin/pharmacology Kinetics Mice Monosaccharide Transport Proteins/genetics RNA/isolation & purification RNA, Messenger/genetics Transcription, Genetic
Chemicals
Deoxy Sugars Insulin Monosaccharide Transport Proteins RNA, Messenger RNA Deoxyglucose
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Garcia de Herreros A
Department of Cellular and Molecular Physiology, Harvard Medical School, Boston, Massachusetts 02115.
Birnbaum M J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1989-11-25
Pages
19994-9
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIDDK NIH HHS · DK39519 · United States
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