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NTCP重组体外HBV感染系统

NTCP-Reconstituted In Vitro HBV Infection System.

作者信息

Sun Yinyan, Qi Yonghe, Peng Bo, Li Wenhui

机构信息

National Institute of Biological Sciences, Beijing, 102206, China.

Graduate Program in School of Life Sciences, Peking University, Beijing, 100871, China.

出版信息

Methods Mol Biol. 2017;1540:1-14. doi: 10.1007/978-1-4939-6700-1_1.

Abstract

Sodium taurocholate cotransporting polypeptide (NTCP) has been identified as a functional receptor for hepatitis B virus (HBV). Expressing human NTCP in human hepatoma HepG2 cells (HepG2-NTCP) renders these cells susceptible for HBV infection. The HepG2-NTCP stably transfected cell line provides a much-needed and easily accessible platform for studying the virus. HepG2-NTCP cells could also be used to identify chemicals targeting key steps of the virus life cycle including HBV covalent closed circular (ccc) DNA, and enable the development of novel antivirals against the infection.Many factors may contribute to the efficiency of HBV infection on HepG2-NTCP cells, with clonal differences among cell line isolates, the source of viral inoculum, and infection medium among the most critical ones. Here, we provide detailed protocols for efficient HBV infection of HepG2-NTCP cells in culture; generation and selection of single cell clones of HepG2-NTCP; production of infectious HBV virion stock through DNA transfection of recombinant plasmid that enables studying primary clinical HBV isolates; and assessing the infection with immunostaining of HBV antigens and Southern blot analysis of HBV cccDNA.

摘要

牛磺胆酸钠共转运多肽(NTCP)已被确定为乙型肝炎病毒(HBV)的功能性受体。在人肝癌HepG2细胞(HepG2-NTCP)中表达人NTCP可使这些细胞易受HBV感染。稳定转染的HepG2-NTCP细胞系为研究该病毒提供了一个急需且易于获得的平台。HepG2-NTCP细胞还可用于鉴定针对病毒生命周期关键步骤的化学物质,包括HBV共价闭合环状(ccc)DNA,并有助于开发针对该感染的新型抗病毒药物。许多因素可能影响HBV对HepG2-NTCP细胞的感染效率,其中细胞系分离株之间的克隆差异、病毒接种物来源以及感染培养基是最关键的因素。在此,我们提供了在培养中高效感染HepG2-NTCP细胞的详细方案;HepG2-NTCP单细胞克隆的生成和筛选;通过重组质粒DNA转染生产传染性HBV病毒粒子储备液,从而能够研究原发性临床HBV分离株;以及通过HBV抗原免疫染色和HBV cccDNA Southern印迹分析评估感染情况。

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