Signal transduction due to HIV-1 envelope interactions with chemokine receptors CXCR4 or CCR5

被引:334
作者
Davis, CB
Dikic, I
Unutmaz, D
Hill, CM
Arthos, J
Siani, MA
Thompson, DA
Schlessinger, J
Littman, DR
机构
[1] NYU,MED CTR,HOWARD HUGHES MED INST,NEW YORK,NY 10016
[2] NYU,MED CTR,DEPT PHARMACOL,NEW YORK,NY 10016
[3] NIAID,NIH,BETHESDA,MD 20892
[4] GRYPHON SCI,S SAN FRANCISCO,CA 94080
关键词
D O I
10.1084/jem.186.10.1793
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Infection with HIV-1 requires expression of CD4 and the chemokine receptors CXCR4 or CCR5 at the target cell surface. Engagement of these receptors by the HIV-1 envelope glycoprotein is essential for membrane fusion, but may additionally activate intracellular signaling pathways. In this study, we demonstrate that chemokines and HIV-1 envelope glycoproteins from both T-tropic and macrophage-tropic strains rapidly induce tyrosine phosphorylation of the protein tyrosine kinase Pyk2. The response requires CXCR3 and CCR5 to be accessible on the cell surface. The results presented here provide the first evidence for activation of an intracellular signaling event that can initiate multiple signaling pathways as a consequence of contact between HIV-1 and chemokine receptors.
引用
收藏
页码:1793 / 1798
页数:6
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