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用克隆的病毒DNA转染后,鸭乙型肝炎病毒在两种分化的人肝癌细胞系中的复制。

Replication of duck hepatitis B virus in two differentiated human hepatoma cell lines after transfection with cloned viral DNA.

作者信息

Hirsch R, Colgrove R, Ganem D

机构信息

Department of Biochemistry and Biophysics, University of California Medical Center, San Francisco 94143.

出版信息

Virology. 1988 Nov;167(1):136-42. doi: 10.1016/0042-6822(88)90062-1.

Abstract

Cloned DNA of duck hepatitis B virus (DHBV) was used to transfect two differentiated human hepatoma cell lines, Huh 7 and Hep G2. Use of the transfected genome as a transcriptional template was demonstrated by the appearance of virus-specific subgenomic and genomic transcripts. Comparison of the steady-state ratio of subgenomic to genomic transcripts in Huh 7 and Hep G2 cells suggests that there are differences in the relative stability and/or rate of production of these transcripts between these cell lines. Viral genomic replication proceeded in both lines, as judged by the presence of DHBV DNA replicative intermediates in cytoplasmic core particles; the levels of these replicative intermediates is roughly equivalent in Huh 7 and Hep G2 cells. Subcutaneous injection of tissue culture medium from transfected Huh 7 cells into Pekin ducks resulted in productive DHBV infection, indicating the production and export of biologically active virus. These cell lines should provide a valuable system for studying the molecular mechanisms of the hepadnaviral life cycle.

摘要

鸭乙型肝炎病毒(DHBV)的克隆DNA被用于转染两种分化的人肝癌细胞系,Huh 7和Hep G2。病毒特异性亚基因组和基因组转录本的出现证明了转染基因组作为转录模板的作用。对Huh 7和Hep G2细胞中亚基因组与基因组转录本的稳态比率进行比较表明,这些细胞系之间这些转录本的相对稳定性和/或产生速率存在差异。通过细胞质核心颗粒中DHBV DNA复制中间体的存在判断,病毒基因组复制在两种细胞系中均有进行;这些复制中间体的水平在Huh 7和Hep G2细胞中大致相当。将转染的Huh 7细胞的组织培养基皮下注射到北京鸭中导致了有生产性的DHBV感染,表明产生并分泌了具有生物活性的病毒。这些细胞系应为研究嗜肝DNA病毒生命周期的分子机制提供一个有价值的系统。

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