THE DIFFERENCE IN GP160 AND GP120 OF HIV TYPE-1 IN THE INDUCTION OF CD4 DOWN-REGULATION PRECEDING SINGLE-CELL KILLING

被引:23
作者
KOGA, Y
NAKAMURA, K
SASAKI, M
KIMURA, G
NOMOTO, K
机构
[1] KYUSHU UNIV,MED INST BIOREGULAT,DEPT IMMUNOL,FUKUOKA 812,JAPAN
[2] KYUSHU UNIV,MED INST BIOREGULAT,DEPT VIROL,FUKUOKA 812,JAPAN
关键词
D O I
10.1006/viro.1994.1274
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The human immunodeficiency virus type 1 (HIV-I) 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. (C) 1994 Academic Press, Inc.
引用
收藏
页码:137 / 141
页数:5
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