APOPTOSIS AS A MECHANISM OF CELL-DEATH IN CULTURED T-LYMPHOBLASTS ACUTELY INFECTED WITH HIV-1

被引:414
作者
TERAI, C
KORNBLUTH, RS
PAUZA, CD
RICHMAN, DD
CARSON, DA
机构
[1] UNIV CALIF SAN DIEGO,DEPT MED,S-045,LA JOLLA,CA 92093
[2] UNIV CALIF SAN DIEGO,DEPT PATHOL,LA JOLLA,CA 92093
[3] UNIV CALIF SAN DIEGO,SAM & ROSE STEIN INST RES AGING,LA JOLLA,CA 92093
[4] UNIV WISCONSIN,SCH MED,DEPT PATHOL & LAB MED,MADISON,WI 53706
关键词
AIDS; PROGRAMMED CELL DEATH; MT2; CELL; GP120; DNA FRAGMENTATION;
D O I
10.1172/JCI115188
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The mechanisms by which HIV-1 infection kills T lymphocytes are not clearly established. Apoptosis is an internally programmed cell death pathway that may regulate both T cell development and senescence, and that is characterized by cleavage of DNA at internucleosomal regions. The present experiments show that acute HIV-1 infection of MT2 lymphoblasts and activated normal peripheral blood mononuclear cells induces apoptosis. The addition of anti-gp 120 neutralizing antibody, after HIV-1 infection of MT2 cells, permitted sustained high levels of viral replication, but blocked apoptosis and cell death. Apoptosis may account for the direct cytopathologic effects of HIV-1 in T cells.
引用
收藏
页码:1710 / 1715
页数:6
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