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PMID: 1518840 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Glucose and glucosamine regulate growth factor gene expression in vascular smooth muscle cells.

McClain DA, Paterson AJ, Roos MD, Wei X, Kudlow JE

Abstract

We have investigated the regulation of the expression of two growth factors found in vascular smooth muscle, transforming growth factor alpha (TGF alpha) and basic fibroblast growth factor (bFGF). Cells cultured in medium containing 30 mM glucose exhibited a 2-fold increase in TGF alpha mRNA and a 3-fold increase in bFGF mRNA compared with cells grown in normal (5.5 mM) glucose. Glucosamine was more potent than glucose, leading to a 6-fold increase in TGF alpha mRNA. TGF alpha protein levels were also increased by glucosamine treatment, and the predominant species present was the membrane-bound precursor form of TGF alpha. To examine further the regulation of growth factors by sugars, cultured rat aortic smooth muscle cells were transfected with a plasmid construct consisting of a 1.2-kilobase-pair fragment of the TGF alpha promoter linked to a luciferase reporter gene. Increasing the concentration of glucose in the culture medium from 5.5 mM to 30 mM led to a rapid, 1.7-fold increase in the activity of the TGF alpha promoter. Glucosamine was much more potent than glucose in this stimulation, with 2 mM glucosamine causing a 12-fold increase in TGF alpha promoter activity. Insulin had no effect on luciferase activity in either the presence or the absence of added sugars. The glucose response element of the TGF alpha gene maps to a 130-base-pair segment that includes three potential binding sites for the transcription factor Sp1. We conclude that high glucose concentrations such as are reached in diabetes mellitus can stimulate the transcription of the genes for growth factors in vascular smooth muscle cells. This signaling pathway apparently involves the metabolism of glucose to glucosamine. This effect could be representative of nutritional regulation of a family of genes and could contribute to the toxicity of hyperglycemia and the vascular complications of diabetes.

MeSH Terms
Animals Cells, Cultured DNA Mutational Analysis Fibroblast Growth Factor 2/genetics Gene Expression Regulation/drug effects Genes Glucosamine/pharmacology Glucose/pharmacology In Vitro Techniques Muscle, Smooth, Vascular/physiology Promoter Regions, Genetic RNA, Messenger/genetics Rats Transcription, Genetic/drug effects Transforming Growth Factor alpha/genetics
Chemicals
RNA, Messenger Transforming Growth Factor alpha Fibroblast Growth Factor 2 Glucose Glucosamine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
McClain D A
Department of Medicine, University of Alabama, Birmingham 35294.
Paterson A J
Roos M D
Wei X
Kudlow J E
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34 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1992-09-01
Pages
8150-4
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC49874
Subset
IM
Grants
NIDDK NIH HHS · DK43526 · United States
NIDDK NIH HHS · DK43652 · United States
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