Dewhurst S, Sakai K, Zhang X H, Wasiak A, Volsky D J
Molecular Virology Laboratory, St. Lukes/Roosevelt Hospital Center, New York, New York.
Virology. 1988 Jan;162(1):151-9. doi: 10.1016/0042-6822(88)90404-7.
Human malignant glioma cells were cotransfected with an infectious molecular clone of the human immunodeficiency virus (HIV) and a selectable drug resistance gene (neo). HIV/neo-positive cell clones were maintained in continuous culture for over 5 months and showed the following characteristics: (i) expression of HIV antigens as detected by indirect immunofluorescence staining in 80-90% of cells; (ii) efficient production of HIV RNA and infectious progeny virus; (iii) minimal cytopathic effects (notably in cell morphology), in contrast to HIV-infected T lymphocytes. These results demonstrate that certain glial cells originating from human brain can support a chronic infection with HIV comparable to that observed in T lymphoid cell lines. The cell lines provide an in vitro model system for studies on the mechanism and biological effects of HIV infection in glial cells, and offer an alternative source of the virus that has not been Adapted to lymphocytes or macrophages.
将人类恶性胶质瘤细胞与人免疫缺陷病毒(HIV)的感染性分子克隆和一个可选的耐药基因(neo)共转染。HIV/neo阳性细胞克隆在连续培养中维持了5个多月,并表现出以下特征:(i)通过间接免疫荧光染色在80-90%的细胞中检测到HIV抗原的表达;(ii)高效产生HIV RNA和有感染性的子代病毒;(iii)与HIV感染的T淋巴细胞相比,细胞病变效应最小(特别是在细胞形态方面)。这些结果表明,源自人脑的某些胶质细胞能够支持与在T淋巴细胞系中观察到的类似的HIV慢性感染。这些细胞系为研究HIV感染胶质细胞的机制和生物学效应提供了一个体外模型系统,并提供了一种尚未适应淋巴细胞或巨噬细胞的病毒的替代来源。