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{"title":"Hepatitis C Virus Infection of Cultured Cells and Primary Human Hepatocytes","authors":"Brianna Lowey, Qisheng Li","doi":"10.1002/cpcb.54","DOIUrl":null,"url":null,"abstract":"<p>Hepatitis C virus (HCV) is a positive-sense, single-stranded RNA virus in the family <i>Flaviviridae</i> with specific hepatotropism. HCV poses a significant health burden worldwide, frequently causing chronic infections associated with progressive liver damage and various extrahepatic manifestations. In recent years, the development of several permissive cell culture (HCVcc) systems has allowed for <i>in vitro</i> propagation of HCV, study of the viral life cycle and virus–host interactions, and identification of novel antivirals. Here we describe the use of human hepatoma cell lines Huh7 and HepG2/CD81/miR-122, as well as primary human hepatocytes (PHHs), for HCV infection and propagation. We also provide protocols for the quantitative analysis of intracellular and extracellular HCV RNA and detection of HCV core protein expression by immunostaining. In addition, we describe methods to manipulate cellular gene expression, including transfection of small interfering RNAs (siRNAs) targeting HCV host factors or overexpressing cellular microRNAs in hepatocytes, to assess their effects on productive HCV infection and liver pathogenesis. © 2018 by John Wiley & Sons, Inc.</p>","PeriodicalId":40051,"journal":{"name":"Current Protocols in Cell Biology","volume":"80 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpcb.54","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Cell Biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpcb.54","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
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Abstract
Hepatitis C virus (HCV) is a positive-sense, single-stranded RNA virus in the family Flaviviridae with specific hepatotropism. HCV poses a significant health burden worldwide, frequently causing chronic infections associated with progressive liver damage and various extrahepatic manifestations. In recent years, the development of several permissive cell culture (HCVcc) systems has allowed for in vitro propagation of HCV, study of the viral life cycle and virus–host interactions, and identification of novel antivirals. Here we describe the use of human hepatoma cell lines Huh7 and HepG2/CD81/miR-122, as well as primary human hepatocytes (PHHs), for HCV infection and propagation. We also provide protocols for the quantitative analysis of intracellular and extracellular HCV RNA and detection of HCV core protein expression by immunostaining. In addition, we describe methods to manipulate cellular gene expression, including transfection of small interfering RNAs (siRNAs) targeting HCV host factors or overexpressing cellular microRNAs in hepatocytes, to assess their effects on productive HCV infection and liver pathogenesis. © 2018 by John Wiley & Sons, Inc.
培养细胞和原代人肝细胞的丙型肝炎病毒感染
丙型肝炎病毒(HCV)是黄病毒科的一种阳性单链RNA病毒,具有特异性嗜肝性。丙型肝炎病毒在世界范围内造成严重的健康负担,经常引起与进行性肝损害和各种肝外表现相关的慢性感染。近年来,几种允许细胞培养(HCVcc)系统的发展使得HCV的体外繁殖、病毒生命周期和病毒-宿主相互作用的研究以及新型抗病毒药物的鉴定成为可能。在这里,我们描述了使用人肝癌细胞系Huh7和HepG2/CD81/miR-122,以及原代人肝细胞(phh),用于HCV感染和繁殖。我们还提供了细胞内和细胞外HCV RNA的定量分析方案,并通过免疫染色检测HCV核心蛋白的表达。此外,我们描述了操纵细胞基因表达的方法,包括转染靶向HCV宿主因子的小干扰rna (sirna)或在肝细胞中过表达细胞microrna,以评估其对生产性HCV感染和肝脏发病机制的影响。©2018 by John Wiley &儿子,Inc。
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