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肝脏脂质分子诱导磷酸烯醇式丙酮酸羧激酶(细胞溶质型)基因转录并减弱胰岛素作用。

Liver lipid molecules induce PEPCK-C gene transcription and attenuate insulin action.

作者信息

Chen Guoxun

机构信息

Department of Nutrition, The University of Tennessee at Knoxville, 229 Jessie Harris Building, 1215 West Cumberland Avenue, Knoxville, TN 37996, USA.

出版信息

Biochem Biophys Res Commun. 2007 Sep 28;361(3):805-10. doi: 10.1016/j.bbrc.2007.07.108. Epub 2007 Jul 27.

Abstract

Cytosolic phosphoenolpyruvate carboxykinase (PEPCK-C) plays key roles in gluconeogenesis, glyceroneogenesis, and cataplerosis. Experiments were designed to examine the effects of endogenous lipid molecules from rat livers on the expression of PEPCK-C gene in primary rat hepatocytes. The lipid extracts prepared from livers of Zucker fatty, lean, and Wistar rats induced the expression levels of PEPCK-C transcripts. Insulin-mediated reduction of PEPCK-C gene expression was attenuated by the same treatment. The lipid extracts induced the relative luciferase activity of reporter gene constructs that contain a 2.2-kb 5' promoter fragment of PEPCK-C gene, but not the construct that contains only the 3' untranslated region (UTR) of its mRNA. The estimated half life of PEPCK-C transcripts in the presence of the lipid extract is the same as that in the absence of it. My results demonstrate for the first time that endogenous lipid molecules induce PEPCK-C gene transcription and attenuate insulin action in liver.

摘要

胞质磷酸烯醇式丙酮酸羧激酶(PEPCK-C)在糖异生、甘油生成和回补反应中起关键作用。本实验旨在研究大鼠肝脏内源性脂质分子对原代大鼠肝细胞中PEPCK-C基因表达的影响。从 Zucker 肥胖大鼠、瘦大鼠和 Wistar 大鼠肝脏中提取的脂质提取物可诱导 PEPCK-C 转录本的表达水平。相同处理可减弱胰岛素介导的 PEPCK-C 基因表达降低。脂质提取物可诱导含有 PEPCK-C 基因 2.2 kb 5'启动子片段的报告基因构建体的相对荧光素酶活性,但对仅含有其 mRNA 3'非翻译区(UTR)的构建体无此作用。在有脂质提取物存在的情况下,PEPCK-C 转录本的估计半衰期与无脂质提取物时相同。我的研究结果首次证明内源性脂质分子可诱导肝脏中 PEPCK-C 基因转录并减弱胰岛素作用。

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