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首页> 外文期刊>BioMed research international >Human Cytomegalovirus-Encoded miR-US25-l Aggravates the Oxidised Low Density Lipoprotein-Induced Apoptosis of Endothelial Cells
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Human Cytomegalovirus-Encoded miR-US25-l Aggravates the Oxidised Low Density Lipoprotein-Induced Apoptosis of Endothelial Cells

机译:人类巨细胞病毒编码的miR-US25-1加重了氧化的低密度脂蛋白诱导的内皮细胞凋亡。

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Human cytomegalovirus (HCMV) infection is linked to the development and severity of the cardiovascular disease atherosclerosis; however, there is little known about the promotion of atherosclerosis. miR-US25-l is one of HCMV-encoded miRNAs and targets cellular genes that are essential for virus growth to control the life cycle of the virus and host cells. The prominent regulation on cell cycle genes of the miR-US25-l attracts us to explore its role in the atherosclerosis promotion. It was indicated that miR-US25-1 level was upregulated in subjects or in endothelial cells with HCMV infection; and the miR-US25-l downregulated the expression of BRCC 3 by targeting the 5' UTR of BRCC 3. And a miR-US25-l mimics transfection could reduce the EAhy926 cell viability but did not induce apoptosis in EAhy926 cells. And what is more, miR-US25-l mimicis transfection deteriorated the ox-LDL-induced apoptosis and aggravated the upregulation of apoptosis-associated molecules by oxidised low density lipoprotein (ox-LDL) in EAhy926 cells. And we have also confirmed the deregulation of BRCC 3 expression by miR-US25-l by targeting the 5' UTR of it. Given the vital role of BRCC 3 in DNA damage repairing, we speculated that the targeting inhibition of BRCC 3 by miR-US25-l may contribute to the aggravation of ox-LDL-promoted apoptosis of endothelial EAhy926 cells.
机译:人类巨细胞病毒(HCMV)感染与心血管疾病动脉粥样硬化的发展和严重程度有关;但是,关于动脉粥样硬化的促进知之甚少。 miR-US25-1是HCMV编码的miRNA之一,并靶向对于病毒生长至关重要的细胞基因,以控制病毒和宿主细胞的生命周期。 miR-US25-1对细胞周期基因的突出调控吸引了我们探索其在促进动脉粥样硬化中的作用。结果表明,受HCMV感染的受试者或内皮细胞中的miR-US25-1水平上调; miR-US25-1通过靶向BRCC 3的5'UTR下调BRCC 3的表达。miR-US25-1模拟转染可以降低EAhy926细胞的活力,但不诱导EAhy926细胞凋亡。而且,miR-US25-1模仿物转染可恶化ox-LDL诱导的凋亡,并加剧EAhy926细胞中氧化的低密度脂蛋白(ox-LDL)对凋亡相关分子的上调。并且我们还证实了miR-US25-1通过靶向BRCC 3的5'UTR来解除其表达。考虑到BRCC 3在DNA损伤修复中的重要作用,我们推测miR-US25-1对BRCC 3的靶向抑制作用可能会加剧ox-LDL促进的内皮EAhy926细胞凋亡。

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