Li Jinping, Takaishi Kiyosumi, Cook William, McCorkle Sara Kay, Unger Roger H
Touchstone Center for Diabetes Research, University of Texas Southwestern Medical Center and Veterans Affairs Medical Center, Dallas, TX 75390, USA.
Proc Natl Acad Sci U S A. 2003 Aug 5;100(16):9476-81. doi: 10.1073/pnas.1133426100. Epub 2003 Jul 17.
We have examined gene expression in the fat tissue of normal mice at the onset of diet-induced obesity. Insulin-induced gene 1 (insig-1) mRNA rose progressively with a high-fat diet and declined on a restricted diet. Because insig-1 binds sterol regulatory element-binding protein cleavage-activating protein in the endoplasmic reticulum, thereby blocking proteolytic processing required for sterol regulatory element-binding protein activation, we tested its influence on lipogenesis. In differentiating 3T3-L1 cells, insig-1 and -2 rose in parallel with aP2 mRNA during differentiation. The mRNA of the lipogenic transcription factor, carbohydrate response element-binding protein, was undetectable in undifferentiated 3T3-L1 preadipocytes but rose dramatically during differentiation in 25 mM, but not in 5 mM, glucose. Transfection of mouse or human insig-1 into 3T3-L1 preadipocytes completely prevented oil red O staining and blocked upregulation of aP2, peroxisome proliferator-activated receptor gamma2, and carbohydrate response element-binding protein, while reducing down-regulation of preadipocyte factor 1. The results suggest that insig-1 expression restricts lipogenesis in mature adipocytes and blocks differentiation in preadipocytes.
我们检测了饮食诱导肥胖开始时正常小鼠脂肪组织中的基因表达。胰岛素诱导基因1(insig-1)mRNA在高脂饮食时逐渐升高,而在限制饮食时下降。由于insig-1在内质网中与固醇调节元件结合蛋白裂解激活蛋白结合,从而阻断固醇调节元件结合蛋白激活所需的蛋白水解过程,我们测试了其对脂肪生成的影响。在分化的3T3-L1细胞中,insig-1和-2在分化过程中与aP2 mRNA平行升高。脂肪生成转录因子碳水化合物反应元件结合蛋白的mRNA在未分化的3T3-L1前脂肪细胞中无法检测到,但在25 mM而非5 mM葡萄糖的分化过程中显著升高。将小鼠或人类insig-1转染到3T3-L1前脂肪细胞中可完全阻止油红O染色,并阻断aP2、过氧化物酶体增殖物激活受体γ2和碳水化合物反应元件结合蛋白的上调,同时减少前脂肪细胞因子1的下调。结果表明,insig-1表达限制成熟脂肪细胞中的脂肪生成,并阻断前脂肪细胞的分化。