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脂肪细胞分化与决定因子1/固醇调节元件结合蛋白1对过氧化物酶体增殖物激活受体γ表达的调控:对脂肪细胞分化和代谢的影响

Regulation of peroxisome proliferator-activated receptor gamma expression by adipocyte differentiation and determination factor 1/sterol regulatory element binding protein 1: implications for adipocyte differentiation and metabolism.

作者信息

Fajas L, Schoonjans K, Gelman L, Kim J B, Najib J, Martin G, Fruchart J C, Briggs M, Spiegelman B M, Auwerx J

机构信息

LBRE, U 325 INSERM, Institut Pasteur, F-59019 Lille, France.

出版信息

Mol Cell Biol. 1999 Aug;19(8):5495-503. doi: 10.1128/MCB.19.8.5495.

Abstract

Peroxisome proliferator-activated receptor gamma (PPARgamma) is a nuclear receptor implicated in adipocyte differentiation and insulin sensitivity. We investigated whether PPARgamma expression is dependent on the activity of adipocyte differentiation and determination factor 1/sterol regulatory element binding protein 1 (ADD-1/SREBP-1), another transcription factor associated with both adipocyte differentiation and cholesterol homeostasis. Ectopic expression of ADD-1/SREBP-1 in 3T3-L1 and HepG2 cells induced endogenous PPARgamma mRNA levels. The related transcription factor SREBP-2 likewise induced PPARgamma expression. In addition, cholesterol depletion, a condition known to result in proteolytic activation of transcription factors of the SREBP family, induced PPARgamma expression and improved PPRE-driven transcription. The effect of the SREBPs on PPARgamma expression was mediated through the PPARgamma1 and -3 promoters. Both promoters contain a consensus E-box motif that mediates the regulation of the PPARgamma gene by ADD-1/SREBP-1 and SREBP-2. These results suggest that PPARgamma expression can be controlled by the SREBP family of transcription factors and demonstrate new interactions between transcription factors that can regulate different pathways of lipid metabolism.

摘要

过氧化物酶体增殖物激活受体γ(PPARγ)是一种与脂肪细胞分化和胰岛素敏感性相关的核受体。我们研究了PPARγ的表达是否依赖于脂肪细胞分化和决定因子1/固醇调节元件结合蛋白1(ADD-1/SREBP-1)的活性,ADD-1/SREBP-1是另一种与脂肪细胞分化和胆固醇稳态相关的转录因子。在3T3-L1和HepG2细胞中异位表达ADD-1/SREBP-1可诱导内源性PPARγ mRNA水平。相关转录因子SREBP-2同样可诱导PPARγ表达。此外,胆固醇耗竭是一种已知会导致SREBP家族转录因子发生蛋白水解激活的情况,它可诱导PPARγ表达并改善PPRE驱动的转录。SREBPs对PPARγ表达的影响是通过PPARγ1和-3启动子介导的。这两个启动子都含有一个共有E-box基序,该基序介导ADD-1/SREBP-1和SREBP-2对PPARγ基因的调控。这些结果表明,PPARγ的表达可由SREBP转录因子家族控制,并证明了可调节不同脂质代谢途径的转录因子之间存在新的相互作用。

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