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由于HIV-1包膜与趋化因子受体CXCR4或CCR5相互作用而导致的信号转导。

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

作者信息

Davis C B, Dikic I, Unutmaz D, Hill C M, Arthos J, Siani M A, Thompson D A, Schlessinger J, Littman D R

机构信息

Division of Molecular Pathogenesis, Skirball Institute for Biomolecular Medicine, NYU Medical Center 10016, USA.

出版信息

J Exp Med. 1997 Nov 17;186(10):1793-8. doi: 10.1084/jem.186.10.1793.

Abstract

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 CXCR4 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.

摘要

感染HIV-1需要在靶细胞表面表达CD4和趋化因子受体CXCR4或CCR5。HIV-1包膜糖蛋白与这些受体的结合对于膜融合至关重要,但也可能额外激活细胞内信号通路。在本研究中,我们证明来自T嗜性和巨噬细胞嗜性毒株的趋化因子和HIV-1包膜糖蛋白能迅速诱导蛋白酪氨酸激酶Pyk2的酪氨酸磷酸化。该反应要求CXCR4和CCR5在细胞表面可及。此处给出的结果首次证明了一种细胞内信号事件的激活,该事件可因HIV-1与趋化因子受体接触而启动多条信号通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/637e/2199136/883450a855b4/JEM.971343f1a.jpg

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