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极低密度脂蛋白(VLDL)和β-极低密度脂蛋白(β-VLDL)诱导的VLDL受体表达及其信号通路的上调。

Up-regulation of VLDL receptor expression and its signaling pathway induced by VLDL and beta-VLDL.

作者信息

Liu Zhiguo, Li He, Li Yinghong, Wang Yan, Zong Yiqiang, Feng Youmei, Feng Zongchen, Deng Yaozu, Qu Shen

机构信息

Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

J Huazhong Univ Sci Technolog Med Sci. 2009 Feb;29(1):1-7. doi: 10.1007/s11596-009-0101-9. Epub 2009 Feb 18.

Abstract

Very low density lipoprotein receptor (VLDLR) is thought to participate in the pathogenesis of atherosclerosis induced by VLDL and beta-VLDL. The present study was undertaken to elucidate the effects of VLDL and beta-VLDL on VLDLR expression and its signaling pathway. RAW264.7 cells were incubated with VLDL and beta-VLDL. The expression of VLDLR mRNA was detected by RT-PCR. The transcriptional activity of VLDLR gene was detected in recombinant plasmid pGL4.2VR-luciferase transfected RAW264.7. Western blot assay was used to detect the changes of phosphorylated ERK1/2 protein. Inhibitors or activators were used to observe the signal pathway involving VLDLR expression regulation. The results showed that VLDL and beta-VLDL stimulated ERK1/2 activity in a PKC-dependent manner. VLDL or beta-VLDL-induced VLDLR expression on macrophages was extremely abolished by inhibitors ERK1/2 or PKC. Our findings revealed that VLDL or beta-VLDL-induced VLDLR expression via PKC/ERK cascades and the effect was linked to the transcriptional activation of VLDLR gene promoter.

摘要

极低密度脂蛋白受体(VLDLR)被认为参与了由极低密度脂蛋白(VLDL)和β-极低密度脂蛋白(β-VLDL)诱导的动脉粥样硬化的发病机制。本研究旨在阐明VLDL和β-VLDL对VLDLR表达及其信号通路的影响。将RAW264.7细胞与VLDL和β-VLDL一起孵育。通过逆转录聚合酶链反应(RT-PCR)检测VLDLR mRNA的表达。在重组质粒pGL4.2VR-荧光素酶转染的RAW264.7细胞中检测VLDLR基因的转录活性。采用蛋白质免疫印迹法(Western blot assay)检测磷酸化细胞外调节蛋白激酶1/2(ERK1/2)蛋白的变化。使用抑制剂或激活剂来观察涉及VLDLR表达调控的信号通路。结果表明,VLDL和β-VLDL以蛋白激酶C(PKC)依赖的方式刺激ERK1/2活性。ERK1/2或PKC抑制剂可极大地消除VLDL或β-VLDL诱导的巨噬细胞VLDLR表达。我们的研究结果表明,VLDL或β-VLDL通过PKC/ERK级联反应诱导VLDLR表达,且该效应与VLDLR基因启动子的转录激活有关。

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