Membrane raft microdomains mediate lateral assemblies required for HIV-1 infection.

EMBO Rep

Department of Immunology and Oncology, Centro Nacional de Biotecnología/CSIC, Madrid, Spain.

Published: August 2000

HIV-1 infection triggers lateral membrane diffusion following interaction of the viral envelope with cell surface receptors. We show that these membrane changes are necessary for infection, as initial gp120-CD4 engagement leads to redistribution and clustering of membrane microdomains, enabling subsequent interaction of this complex with HIV-1 co-receptors. Disruption of cell membrane rafts by cholesterol depletion before viral exposure inhibits entry by both X4 and R5 strains of HIV-1, although viral replication in infected cells is unaffected by this treatment. This inhibitory effect is fully reversed by cholesterol replenishment of the cell membrane. These results indicate a general mechanism for HIV-1 envelope glycoprotein-mediated fusion by reorganization of membrane microdomains in the target cell, and offer new strategies for preventing HIV-1 infection.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1084257PMC
http://dx.doi.org/10.1093/embo-reports/kvd025DOI Listing

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