Signal Transduction Due to HIV-1 Envelope Interactions with Chemokine Receptors CXCR4 or CCR5

Author:

Davis Craig B.1,Dikic Ivan1,Unutmaz Derya11,Hill C. Mark1,Arthos James1,Siani Michael A.1,Thompson Darren A.1,Schlessinger Joseph1,Littman Dan R.11

Affiliation:

1. From the Division of Molecular Pathogenesis, Skirball Institute for Biomolecular Medicine, Howard Hughes Medical Institute, and Department of Pharmacology, New York University Medical Center, New York 10016; National Institute of Allergy and Infectious Disease, National Institutes of Health, Bethesda, Maryland 20892; and Gryphon Sciences, South San Francisco, California 94080

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.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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