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首页> 外文期刊>Cellular Physiology and Biochemistry >Mipu1 Inhibits Lipid Accumulation Through Down-Regulation of CD36 in RAW264.7 Cells
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Mipu1 Inhibits Lipid Accumulation Through Down-Regulation of CD36 in RAW264.7 Cells

机译:Mipu1通过下调RAW264.7细胞中的CD36抑制脂质积累。

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Background/Aims: Our recent data indicated that Mipu1 overexpression reduces lipid intake and CD36 expression of macrophages in the presence of oxLDL. However, the mechanism of Mipu1 inhibiting lipid accumulation in macrophages is not elucidated. Methods: Real-time quantitative polymerase chain reaction (PCR) and western blot analysis were used to detect expression of Mipu1 and CD36. The promoter activity of CD36 was studied using luciferase assays. Chromatin immunoprecipitation (ChIP) was used to show the recruitment of Mipu1 onto the CD36 promoter. High-performance liquid chromatography and Dil-labeled lipoprotein were used to detect cholesterol accumulation. Results: Here, we show that CD36 overexpression rescues oxLDL-induced cholesterol accumulation in RAW264.7-Mipu1 cells. Analysis of the mouse CD36 promoter revealed two potential Mipu1-response elements (MRE), one of which (from -237bp to -244bp, ACTTAC) was shown, using mutagenesis and deletion analysis, to be functional. Mipu1 was demonstrated to bind to CD36 promoter, and oxLDL treatment resulted in increases in their interaction as assessed by ChIP. Conclusions: It was demonstrated that Mipu1 inhibited the lipid accumulation of macrophages and it down-regulated CD36 expression in the presence of oxLDL.
机译:背景/目的:我们的最新数据表明,在存在oxLDL的情况下,Mipu1的过表达减少了脂质的摄入和巨噬细胞CD36的表达。但是,尚未阐明Mipu1抑制巨噬细胞脂质积累的机制。方法:采用实时定量聚合酶链反应(PCR)和蛋白质印迹分析检测Mipu1和CD36的表达。使用荧光素酶测定法研究了CD36的启动子活性。染色质免疫沉淀(ChIP)用于显示Mipu1在CD36启动子上的募集。高效液相色谱法和Dil标记的脂蛋白用于检测胆固醇积累。结果:在这里,我们表明CD36过表达可以挽救oxLDL诱导的RAW264.7-Mipu1细胞中胆固醇的积累。小鼠CD36启动子的分析揭示了两个潜在的Mipu1反应元件(MRE),其中一个(从-237bp至-244bp,ACTTAC)通过诱变和缺失分析显示具有功能。据ChIP评估,Mipu1被证明与CD36启动子结合,oxLDL处理导致它们的相互作用增加。结论:在有oxLDL的情况下,Mipu1抑制了巨噬细胞的脂质蓄积并下调了CD36的表达。

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