Koga Y, Nakamura K, Sasaki M, Kimura G, Nomoto K
Department of Infectious Disease, School of Medicine, Tohkai University, Kanagawa, Japan.
Virology. 1994 May 15;201(1):137-41. doi: 10.1006/viro.1994.1274.
The human immunodeficiency virus type 1 (HIV-1) envelope glycoprotein is synthesized as a precursor glycoprotein, gp160, and is then processed into gp120 and gp41. In the present study, CD4+ cell clones expressing either gp160 or gp120 of HIV-1 under the transcriptional control of an inducible promoter were made in order to examine the effect of these env products on the downregulation of surface CD4 and cell injury. A complete disappearance of surface CD4 preceding single-cell death occurred in the cell clones expressing gp160, in which a complex between CD4 and gp160 was formed and then accumulated intracellularly. In contrast to this, the cell clones expressing gp120 neither exhibited any such depletion of surface CD4 nor showed any apparent cytopathic effect. Therefore, it is thought that gp160 but not gp120 plays a crucial role in both the downregulation of surface CD4 and the resultant cell death in the cells infected with HIV-1.
人类免疫缺陷病毒1型(HIV-1)包膜糖蛋白最初作为前体糖蛋白gp160合成,随后加工成gp120和gp41。在本研究中,构建了在可诱导启动子转录控制下表达HIV-1的gp160或gp120的CD4+细胞克隆,以研究这些env产物对表面CD4下调和细胞损伤的影响。在表达gp160的细胞克隆中,单细胞死亡前表面CD4完全消失,其中CD4与gp160形成复合物并在细胞内积累。与此相反,表达gp120的细胞克隆既未表现出表面CD4的任何此类消耗,也未显示出任何明显的细胞病变效应。因此,认为gp160而非gp120在感染HIV-1的细胞中表面CD4的下调和由此导致的细胞死亡中起关键作用。