Srinivasakumar N, Chazal N, Helga-Maria C, Prasad S, Hammarskjöld M L, Rekosh D
Myles H. Thaler Center for AIDS and Human Retrovirus Research and Department of Microbiology, University of Virginia, Charlottesville 22908, USA.
J Virol. 1997 Aug;71(8):5841-8. doi: 10.1128/JVI.71.8.5841-5848.1997.
We describe the generation of stable human immunodeficiency virus type 1 (HIV-1)-packaging lines that constitutively express high levels of HIV-1 structural proteins in either a Rev-dependent or a Rev-independent fashion. These cell lines were used to assess gene transfer by using an HIV-1 vector expressing the hygromycin B resistance gene and to study the effects of Rev, Tat, and Nef on the vector titer. The Rev-independent cell lines were created by using gag-pol and env expression vectors that contain the Mason-Pfizer monkey virus (MPMV) constitutive transport element (CTE). Vector titers approaching 10(4) CFU/ml were routinely obtained with these cell lines, as well as with the Rev-dependent cell lines, with HeLa-CD4 cells as targets. The presence of Nef and Tat in the producer cell each increased the vector titer 5- to 10-fold. Rev, on the other hand, was absolutely essential for gene transfer, unless the MPMV CTE was present in the vector. In that case, by using the Rev-independent cell lines for packaging, Rev could be completely eliminated from the system without a reduction in vector titer.
我们描述了稳定的1型人类免疫缺陷病毒(HIV-1)包装细胞系的构建,这些细胞系以依赖Rev或不依赖Rev的方式持续高水平表达HIV-1结构蛋白。这些细胞系用于通过使用表达潮霉素B抗性基因的HIV-1载体评估基因转移,并研究Rev、Tat和Nef对载体滴度的影响。不依赖Rev的细胞系是通过使用含有马森-辉瑞猴病毒(MPMV)组成型转运元件(CTE)的gag-pol和env表达载体构建的。以HeLa-CD4细胞为靶细胞,使用这些细胞系以及依赖Rev的细胞系,常规获得的载体滴度接近10⁴CFU/ml。生产细胞中Nef和Tat的存在各自使载体滴度提高了5至10倍。另一方面,Rev对于基因转移绝对必要,除非载体中存在MPMV CTE。在那种情况下,通过使用不依赖Rev的细胞系进行包装,Rev可以从系统中完全去除而不会降低载体滴度。