Engelking Luke J, Liang Guosheng, Hammer Robert E, Takaishi Kiyosumi, Kuriyama Hiroshi, Evers Bret M, Li Wei-Ping, Horton Jay D, Goldstein Joseph L, Brown Michael S
Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9046, USA.
J Clin Invest. 2005 Sep;115(9):2489-98. doi: 10.1172/JCI25614. Epub 2005 Aug 11.
End-product feedback inhibition of cholesterol synthesis was first demonstrated in living animals by Schoenheimer 72 years ago. Current studies define Insig proteins as essential elements of this feedback system in mouse liver. In cultured cells, Insig proteins are required for sterol-mediated inhibition of the processing of sterol regulatory element-binding proteins (SREBPs) to their nuclear forms. We produced mice with germline disruption of the Insig2 gene and Cre-mediated disruption of the Insig1 gene in liver. On a chow diet, these double-knockout mice overaccumulated cholesterol and triglycerides in liver. Despite this accumulation, levels of nuclear SREBPs and mRNAs for SREBP target genes in lipogenic pathways were not reduced. Whereas cholesterol feeding reduced nuclear SREBPs and lipogenic mRNAs in wild-type mice, this feedback response was severely blunted in the double-knockout mice, and synthesis of cholesterol and fatty acids was not repressed. The amount of HMG-CoA reductase protein was elevated out of proportion to the mRNA in the double-knockout mice, apparently owing to the failure of cholesterol to accelerate degradation of the enzyme. These studies indicate that the essential elements of the regulatory pathway for lipid synthesis function in liver as they do in cultured cells.
72年前,舍恩海默首次在活体动物中证明了胆固醇合成的终产物反馈抑制作用。目前的研究将Insig蛋白定义为小鼠肝脏中这种反馈系统的关键要素。在培养细胞中,Insig蛋白是固醇介导抑制固醇调节元件结合蛋白(SREBPs)加工成其核形式所必需的。我们构建了Insig2基因种系破坏且肝脏中Insig1基因由Cre介导破坏的小鼠。在普通饮食条件下,这些双敲除小鼠肝脏中胆固醇和甘油三酯过度蓄积。尽管有这种蓄积,但核SREBPs水平以及生脂途径中SREBP靶基因的mRNA水平并未降低。在野生型小鼠中,胆固醇喂养可降低核SREBPs和生脂mRNA水平,而在双敲除小鼠中这种反馈反应严重减弱,胆固醇和脂肪酸的合成未受到抑制。在双敲除小鼠中,HMG-CoA还原酶蛋白的量相对于mRNA不成比例地升高,这显然是由于胆固醇未能加速该酶的降解。这些研究表明,肝脏中脂质合成调节途径的关键要素与它们在培养细胞中的作用方式相同。