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胰岛素对HIRc/pCETP-CAT细胞中胆固醇酯转运蛋白(CETP)的启动子没有调节作用。

Insulin does not regulate the promoter of cholesteryl ester transfer protein (CETP) in HIRc/pCETP-CAT cells.

作者信息

MacLean P S, Barakat H A

机构信息

Department of Biochemistry, East Carolina University School of Medicine, Greenville, NC 27858, USA.

出版信息

Mol Cell Biochem. 2000 Aug;211(1-2):1-7. doi: 10.1023/a:1007027818389.

Abstract

Cholesteryl ester transfer protein (CETP) is a plasma enzyme involved in cholesterol metabolism. As a potential target in the treatment of atherosclerosis, a number of studies have focused how this enzyme is regulated. It has been postulated that insulin may regulate CETP gene expression, and these effects may be mediated through CCAAT/enhancer binding protein alpha (C/EBPalpha). The present study examines the effects of insulin on the activity of the CETP promoter in rat fibroblasts expressing the human insulin receptor (HIRc). HIRc cells were stably transfected with a chimeric construct containing 3.2 kb of the CETP promoter attached to the bacterial chloramphenicol acyltransferase gene (pCETP-CAT) without significantly affecting the expression of the insulin receptor. CAT activity was 8-fold higher in cultured HIRc/pCETP-CAT in the presence of 100 mg/dL LDL cholesterol, than those cultured without cholesterol (p < 0.05). However, culturing these cells in the presence of 100 nM insulin did not result in any change in CAT activity when compared to control cells. In HIRc/pCETP-CAT cells transiently transfected with a construct that constitutively expressed C/EBPalpha protein, a 3-fold increase in CAT activity was observed when compared to cells transiently transfected with non-specific DNA (p < 0.05). However, no observable effect on the CETP promoter was observed in the presence of insulin. Thus, in HIRc/pCETP-CAT cells, we were unable to substantiate the hypothesis that insulin regulates CETP gene transcription. These results suggest that the effects of insulin on CETP expression regulation may be downstream of transcription.

摘要

胆固醇酯转运蛋白(CETP)是一种参与胆固醇代谢的血浆酶。作为动脉粥样硬化治疗的潜在靶点,许多研究聚焦于该酶是如何被调节的。据推测,胰岛素可能调节CETP基因表达,且这些作用可能通过CCAAT/增强子结合蛋白α(C/EBPα)介导。本研究检测了胰岛素对表达人胰岛素受体(HIRc)的大鼠成纤维细胞中CETP启动子活性的影响。将含有3.2 kb CETP启动子并连接细菌氯霉素乙酰转移酶基因的嵌合构建体(pCETP-CAT)稳定转染至HIRc细胞,且未显著影响胰岛素受体的表达。在存在100 mg/dL低密度脂蛋白胆固醇的情况下,培养的HIRc/pCETP-CAT细胞中的氯霉素乙酰转移酶(CAT)活性比无胆固醇培养的细胞高8倍(p<0.05)。然而,与对照细胞相比,在100 nM胰岛素存在的情况下培养这些细胞,CAT活性未发生任何变化。在瞬时转染了组成型表达C/EBPα蛋白构建体的HIRc/pCETP-CAT细胞中,与瞬时转染非特异性DNA的细胞相比,观察到CAT活性增加了3倍(p<0.05)。然而,在胰岛素存在的情况下,未观察到对CETP启动子有明显影响。因此,在HIRc/pCETP-CAT细胞中,我们无法证实胰岛素调节CETP基因转录这一假说。这些结果表明,胰岛素对CETP表达调节的作用可能在转录下游。

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