Glucose induces and leptin decreases expression of uncoupling protein-2 mRNA in human islets

被引:45
作者
Brown, JEP [1 ]
Thomas, S [1 ]
Digby, JE [1 ]
Dunmore, SJ [1 ]
机构
[1] Wolverhampton Univ, Sch Appl Sci, Diabet Res Grp, Div Biomed Sci, Wolverhampton WV1 1SB, England
关键词
beta-cell; gene expression; glucose toxicity; type; 2; diabetes;
D O I
10.1016/S0014-5793(02)02296-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Elevated islet uncoupling protein-2 (UCP-2) impairs beta-cell function and UCP-2 may be increased in clinical obesity and diabetes. We investigated the effects of glucose and leptin on UCP-2 expression in isolated human islets. Human islets were incubated for 24 h with glucose (5.5-22 mmol/l) +/- leptin (0-10 nmol/1). Some islet batches were incubated at high (22 mmol/1), and subsequently lower (5.5 mmol/1), glucose to assess reversibility of effects. Leptin effects on insulin release were also measured. Glucose dose-dependently increased UCP-2 expression in all islet batches, maximally by three-fold. This was not fully reversed by subsequently reduced glucose levels. Leptin decreased UCP-2 expression by up to 75%, and maximally inhibited insulin release by 47%, at 22 mmol/1 glucose. This is the first report of UCP-2 expression in human islets and provides novel evidence of its role in the loss of beta-cell function in diabetes. (C) 2002 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:189 / 192
页数:4
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