Autophagy is involved in T cell death after binding of HIV-1 envelope proteins to CXCR4

被引:360
作者
Espert, Lucile
Denizot, Melanie
Grimaldi, Marina
Robert-Hebmann, Veronique
Gay, Bernard
Varbanov, Mihayl
Codogno, Patrice
Biard-Piechaczyk, Martine
机构
[1] CNRS, Lab Infect Retrovirales & Signalisat Cellulaire, UMR 5121, Inst Biol, F-34000 Montpellier, France
[2] INSERM, U504, Villejuif, France
关键词
D O I
10.1172/JCI26185
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
HIV-1 envelope glycoproteins (Env), expressed at the cell surface, induce apoptosis of uninfected CD4(+) T cells, contributing to the development of AIDS. Here we demonstrate that, independently of HIV replication, transfected or HIV-infected cells that express Env induced autophagy and accumulation of Beclin 1 in uninfected CD4(+) T lymphocytes via CXCR4. The same phenomena occurred in a T cell line and in transfected HEK.293 cells that expressed both wild-type CXCR4 and a truncated form of CD4 that is unable to bind the lymphocyte-specific protein kinase Lck. Env-mediated autophagy is required to trigger CD4(+) T cell apoptosis since blockade of autophagy at different steps, by either drugs (3-methyladenine and bafilomycin A1) or siRNAs specific for Beclin 1/Atg6 and Atg7 genes, totally inhibited the apoptotic process. Furthermore, CD4(+) T cells still underwent Env-mediated cell death with autophagic features when apoptosis was inhibited. These results suggest that HIV-infected cells can induce autophagy in bystander CD4(+) T lymphocytes through contact of Env with CXCR4, leading to apoptotic cell death, a mechanism most likely contributing to immunodeficiency.
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页码:2161 / 2172
页数:12
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