Cao Heping, Urban Joseph F, Anderson Richard A
Diet, Genomics, and Immunology Laboratory, Beltsville Human Nutrition Research Center, Agricultural Research Service, US Department of Agriculture, Beltsville, Maryland, USA.
Obesity (Silver Spring). 2008 Jun;16(6):1208-18. doi: 10.1038/oby.2008.65. Epub 2008 Apr 3.
Tristetraprolin (TTP) family proteins (TTP/ZFP36; ZFP36L1, ZFP36L2, ZFP36L3) destabilize adenylate uridylate-rich element-containing mRNAs encoding cytokines, such as tumor necrosis factor (TNF) and vascular endothelial growth factor (VEGF). Little is known about the expression and insulin regulation of TTP and related genes in adipocytes. We analyzed the relative abundance of TTP family mRNAs in 3T3-L1 adipocytes compared to RAW264.7 macrophages and investigated insulin effects on the expression of 43 genes in 3T3-L1 adipocytes.
Insulin was added to mouse 3T3-L1 adipocytes. Relative abundance of mRNA levels was determined by quantitative real-time PCR. TTP and ZFP36L1 proteins were detected by immunoblotting.
Zfp36l1 and Zfp36l2 genes were expressed at eight- to tenfold higher than Ttp in adipocytes. Zfp36l3 mRNA was detected at approximately 1% of Ttp mRNA levels in adipocytes and its low level expression was confirmed in RAW cells. Insulin at 10 and 100 nmol/l increased Ttp mRNA levels by five- to sevenfold, but decreased those of Zfp36l3 by 40% in adipocytes after a 30-min treatment. Immunoblotting showed that insulin induced TTP but did not affect ZFP36L1 protein levels in adipocytes. Insulin decreased mRNA levels of Vegf and a number of other genes in adipocytes.
Insulin induced Ttp mRNA and protein expression and decreased Vegf mRNA levels in adipocytes. Zfp36l3 mRNA was detected, for the first time, in cells other than mouse placenta and extraembryonic tissues. This study established a basis for the investigation of TTP and VEGF genes in the regulation of obesity and suggested that Vegf mRNA may be a target of TTP in fat cells.
锌指蛋白36家族蛋白(TTP/ZFP36;ZFP36L1、ZFP36L2、ZFP36L3)可使编码细胞因子(如肿瘤坏死因子(TNF)和血管内皮生长因子(VEGF))的富含腺苷酸尿苷酸元件的mRNA不稳定。关于脂肪细胞中TTP及相关基因的表达和胰岛素调节作用,人们了解甚少。我们分析了3T3-L1脂肪细胞与RAW264.7巨噬细胞相比,TTP家族mRNA的相对丰度,并研究了胰岛素对3T3-L1脂肪细胞中43个基因表达的影响。
将胰岛素添加到小鼠3T3-L1脂肪细胞中。通过定量实时PCR测定mRNA水平的相对丰度。通过免疫印迹检测TTP和ZFP36L1蛋白。
脂肪细胞中Zfp36l1和Zfp36l2基因的表达比Ttp高8至10倍。在脂肪细胞中检测到Zfp36l3 mRNA的水平约为Ttp mRNA水平的1%,并且在RAW细胞中证实其低水平表达。在30分钟处理后,10和100 nmol/l的胰岛素使脂肪细胞中Ttp mRNA水平增加5至7倍,但使Zfp36l3 mRNA水平降低40%。免疫印迹显示胰岛素诱导脂肪细胞中TTP表达,但不影响ZFP36L1蛋白水平。胰岛素降低了脂肪细胞中Vegf和许多其他基因的mRNA水平。
胰岛素诱导脂肪细胞中Ttp mRNA和蛋白表达,并降低Vegf mRNA水平。首次在小鼠胎盘和胚外组织以外的细胞中检测到Zfp36l3 mRNA。本研究为研究TTP和VEGF基因在肥胖调节中的作用奠定了基础,并提示Vegf mRNA可能是脂肪细胞中TTP的作用靶点。