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miR‐148a and miR‐30a limit HCV‐dependent suppression of the lipid droplet protein, ADRP, in HCV infected cell models

机译:miR-148a和miR-30a限制HCV依赖性抑制脂液滴蛋白,ADRP,在HCV感染细胞模型中

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摘要

Hepatitis C Virus (HCV) promotes lipid droplet (LD) formation and perturbs the expression of the LD associated PAT proteins ADRP and TIP47, to promote its own lifecycle. HCV enhances TIP47 and suppresses ADRP by displacing it from LD surface in infected cell models. We have previously shown that suppression of TIP47 by miR‐148a and miR‐30a decreased intracellular LDs and HCV RNA. Thus, this study aimed at examining whether this microRNA‐mediated suppression of HCV would limit HCV‐dependent displacement of ADRP from LDs. ADRP expression was examined in 21 HCV‐infected liver biopsies and 9 healthy donor liver tissues as well as in HCV‐infected Huh7 cells using qRT‐PCR. miR‐148a and miR‐30a expression was manipulated using specific oligos in JFH‐1 infected, oleic acid treated cells, to study their impact on ADRP expression using qRT‐PCR, and immunofluorescence microscopy. Intracellular HCV RNA was assessed using qRT‐PCR. ADRP is down regulated in patients as well as HCVcc‐JFH‐I infected cell models. Forcing the expression of both miRNAs induced ADRP on the mRNA and protein levels. This study shows that HCV suppresses hepatic ADRP expression in infected patients and cell lines. Forcing the expression of miR‐148a and miR‐30a limits the suppressive effect of HCV on ADRP. J. Med. Virol. 89:653–659, 2017 . ? 2016 Wiley Periodicals, Inc.
机译:丙型肝炎病毒(HCV)促进脂质液滴(LD)形成并渗透LD相关帕特蛋白ADRP和TIP47的表达,以促进其自身的生命周期。 HCV通过从感染的细胞模型中从LD表面移位来增强TIP47并抑制ADRP。我们之前已经表明,MiR-148a和miR-30a的抑制尖端47和miR-30a降低了细胞内LD和HCV RNA。因此,本研究旨在检查该微润罗纳介导的HCV的抑制是否会限制来自LDS的HCV依赖性位移。使用QRT-PCR在21例HCV感染的肝脏活组织检查和9个健康供体肝组织以及HCV感染HUH7细胞中检查ADRP表达。使用JFH-1感染的油酸处理细胞中的特定寡核苷酸操纵miR-148a和miR-30a表达,以使用QRT-PCR和免疫荧光显微镜来研究它们对ADRP表达的影响。使用QRT-PCR评估细胞内HCV RNA。 ADRP在患者以及HCVCC-JFH-I感染的细胞模型中受到调节。迫使两种miRNA的表达诱导mRNA和蛋白质水平的ADRP。本研究表明,HCV抑制了感染患者和细胞系中的肝脏ADRP表达。强制miR-148a和miR-30a的表达限制了HCV对ADRP的抑制作用。 J.Med。病毒。 89:653-659,2017。还2016 Wiley期刊,Inc。

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