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Sp1介导PPARγ激动剂对3T3-L1脂肪细胞中抵抗素基因的抑制作用。

Sp1 mediates repression of the resistin gene by PPARgamma agonists in 3T3-L1 adipocytes.

作者信息

Chung S S, Choi H H, Cho Y M, Lee H K, Park K S

机构信息

Genome Research Center for Diabetes and Endocrine Disease, Clinical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2006 Sep 15;348(1):253-8. doi: 10.1016/j.bbrc.2006.07.048. Epub 2006 Jul 18.

Abstract

Resistin is an adipokine related to obesity and insulin resistance. Expression of the resistin gene is repressed by the treatment of peroxisome proliferator-activated receptor gamma (PPARgamma) agonists, thiazolidinediones (TZDs). In this study, we investigated the mechanism by which TZDs inhibit the resistin gene expression. Resistin gene expression was decreased by TZD in fully differentiated 3T3-L1 adipocytes, which was abolished after treatment of cycloheximide (a protein synthesis inhibitor). TZD could not repress the expression of the resistin gene in the presence of mithramycin A (an Sp1 binding inhibitor). Sp1 binding site of the resistin promoter (-122/-114bp) was necessary for the repression. Further investigation of the effect of TZDs on the modification of Sp1 showed that the level of O-glycosylation of Sp1 was decreased in this process. These results suggest that PPARgamma activation represses the expression of the resistin gene by modulating Sp1 activity.

摘要

抵抗素是一种与肥胖和胰岛素抵抗相关的脂肪因子。过氧化物酶体增殖物激活受体γ(PPARγ)激动剂噻唑烷二酮类(TZDs)可抑制抵抗素基因的表达。在本研究中,我们探究了TZDs抑制抵抗素基因表达的机制。在完全分化的3T3-L1脂肪细胞中,TZDs可降低抵抗素基因的表达,但在用放线菌酮(一种蛋白质合成抑制剂)处理后,这种作用消失。在放线菌素A(一种Sp1结合抑制剂)存在的情况下,TZDs无法抑制抵抗素基因的表达。抵抗素启动子的Sp1结合位点(-122/-114bp)对于这种抑制作用是必需的。进一步研究TZDs对Sp1修饰的影响表明,在此过程中Sp1的O-糖基化水平降低。这些结果表明,PPARγ激活通过调节Sp1活性来抑制抵抗素基因的表达。

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