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可诱导的1型人类免疫缺陷病毒包装细胞系。

Inducible human immunodeficiency virus type 1 packaging cell lines.

作者信息

Yu H, Rabson A B, Kaul M, Ron Y, Dougherty J P

机构信息

Department of Molecular Genetics and Microbiology, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway, New Jersey 08854-5635, USA.

出版信息

J Virol. 1996 Jul;70(7):4530-7. doi: 10.1128/JVI.70.7.4530-4537.1996.

Abstract

Packaging cell lines are important tools for transferring genes into eukaryotic cells. Human immunodeficiency virus type 1 (HIV-1)-based packaging cell lines are difficult to obtain, in part owing to the problem that some HIV-1 proteins are cytotoxic in a variety of cells. To overcome this, we have developed an HIV-1-based packaging cell line which has an inducible expression system. The tetracycline-inducible expression system was utilized to control the expression of the Rev regulatory protein, which in turn controls the expression of the late proteins including Gag, Pol, and Env. Western blotting (immunoblotting) demonstrated that the expression of p24gag and gp120env from the packaging cells peaked on days 6 and 7 postinduction. Reverse transcriptase activity could be detected by day 4 after induction and also peaked on days 6 and 7. Defective vector virus could be propagated, yielding titers as high as 7 x 10(3) CFU/ml, while replication-competent virus was not detectable at any time. Thus, the cell line should enable the transfer of specific genes into CD4+ cells and should be a useful tool for studying the biology of HIV-1. We have also established an inducible HIV-1 Env-expressing cell line which could be used to propagate HIV-1 vectors that require only Env in trans. The env-minus vector virus titer produced from the Env-expressing cells reached 2 x 10(4) CFU/ml. The inducible HIV-1 Env-expressing cell line should be a useful tool for the study of HIV-1 Env as well.

摘要

包装细胞系是将基因导入真核细胞的重要工具。基于1型人类免疫缺陷病毒(HIV-1)的包装细胞系难以获得,部分原因是一些HIV-1蛋白在多种细胞中具有细胞毒性。为克服这一问题,我们开发了一种基于HIV-1的具有诱导表达系统的包装细胞系。利用四环素诱导表达系统来控制Rev调节蛋白的表达,而Rev调节蛋白又控制包括Gag、Pol和Env在内的晚期蛋白的表达。蛋白质印迹法(免疫印迹法)表明,包装细胞中p24gag和gp120env的表达在诱导后第6天和第7天达到峰值。诱导后第4天可检测到逆转录酶活性,其在第6天和第7天也达到峰值。有缺陷的载体病毒能够繁殖,产生的滴度高达7×10³CFU/ml,而在任何时候都检测不到具有复制能力的病毒。因此,该细胞系应能够将特定基因导入CD4⁺细胞,并且应是研究HIV-1生物学的有用工具。我们还建立了一种可诱导表达HIV-1 Env的细胞系,该细胞系可用于繁殖仅需Env反式作用的HIV-1载体。从表达Env的细胞产生的env缺失载体病毒滴度达到2×10⁴CFU/ml。可诱导表达HIV-1 Env的细胞系也应是研究HIV-1 Env的有用工具。

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