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肥胖基因型诱导转染脂肪细胞中GLUT4启动子活性增加:两个脂肪应答区域的描绘及葡萄糖效应

Fatty genotype-induced increase in GLUT4 promoter activity in transfected adipocytes: delineation of two fa-responsive regions and glucose effect.

作者信息

Hainault I, Hajduch E, Lavau M

机构信息

INSERM U177, Unité de Recherches sur la physiopathologie de la Nutrition 15, Paris, France.

出版信息

Biochem Biophys Res Commun. 1995 Apr 26;209(3):1053-61. doi: 10.1006/bbrc.1995.1604.

Abstract

We have previously shown that adipocytes from genetically obese rats exhibited increases in GLUT4 protein and mRNA expressions. In order to elucidate the responsible defect we examined here the activity of GLUT4 promoter using adipocytes transiently transfected with -2212 + 164 rat GLUT4 gene fragment fused to luciferase reporter gene. GLUT4 promoter activity was several-fold higher in obese than in lean rat adipocytes (x4 in suckling 16 days old and x6 in weaned 30 days old rats), demonstrating the implication of transcription factors in the fatty genotype effect on GLUT4 expression. 5' deletion analysis of GLUT4 promoter allowed us to delineate two regions, -907 to -502 and -151 to -68, critical to the genotype effect, suggesting that they harbor fa-response element(s). In lean rat adipocytes GLUT4 promoter activity was not affected by the presence of glucose in the culture medium. In contrast, in obese rat adipocytes GLUT4 transcriptional activity was increased 3-fold from 0 to 5mM glucose, the concentration required for the full genotype effect, suggesting interactions between glucose and fa-dependent GLUT4 transactivator(s).

摘要

我们之前已经表明,遗传性肥胖大鼠的脂肪细胞中GLUT4蛋白和mRNA表达增加。为了阐明其中的缺陷,我们在此使用瞬时转染了与荧光素酶报告基因融合的-2212 + 164大鼠GLUT4基因片段的脂肪细胞,检测了GLUT4启动子的活性。肥胖大鼠脂肪细胞中的GLUT4启动子活性比瘦大鼠脂肪细胞高几倍(16日龄哺乳期大鼠中高4倍,30日龄断奶大鼠中高6倍),这表明转录因子参与了脂肪基因型对GLUT4表达的影响。对GLUT4启动子进行5'缺失分析使我们能够确定两个对基因型效应至关重要的区域,即-907至-502和-151至-68,这表明它们含有脂肪反应元件。在瘦大鼠脂肪细胞中,培养基中葡萄糖的存在不影响GLUT4启动子活性。相反,在肥胖大鼠脂肪细胞中,从0到5mM葡萄糖(产生完全基因型效应所需的浓度),GLUT4转录活性增加了3倍,这表明葡萄糖与脂肪依赖性GLUT4反式激活因子之间存在相互作用。

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