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Tetraspanins CD9 and CD81 Modulate HIV-1-Induced Membrane Fusion
Author(s) -
Mónica GordónAlonso,
Marı́a Yáñez-Mó,
Olga Barreiro,
Susana Álvarez,
María Ángeles MuñozFernández,
Agustı́n Valenzuela-Fernández,
Francisco SánchezMadrid
Publication year - 2006
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.177.8.5129
Subject(s) - tetraspanin , cd81 , syncytium , microbiology and biotechnology , cell fusion , transmembrane protein , lipid bilayer fusion , viral entry , biology , gp41 , viral envelope , membrane protein , virology , cell , receptor , membrane , human immunodeficiency virus (hiv) , virus , viral replication , antigen , epitope , biochemistry , immunology , hepatitis c virus
Protein organization on the membrane of target cells may modulate HIV-1 transmission. Since the tetraspanin CD81 is associated to CD4, the receptor of HIV-1 envelope protein (Env; gp120/gp41), we have explored the possibility that this molecule may modulate the initial steps of HIV-1 infection. On the other hand, CD81 belongs to the tetraspanin family, which has been described as organizers of protein microdomains on the plasma membrane. Therefore, the role of CD81 and other related tetraspanin, CD9, on the cell-to-cell fusion process mediated by HIV-1 was studied. We found that anti-tetraspanin Abs enhanced the syncytia formation induced by HIV-1 envelope proteins and viral entry in human T lymphoblasts. In addition, anti-CD81 Abs triggered its clustering in patches, where CD4 and CXCR4 were included. Moreover, the knocking down of CD81 and CD9 expression resulted in an increase in syncytia formation and viral entry. Accordingly, overexpression of CD81 and CD9 rendered cells less susceptible to Env-mediated syncytia formation. These data indicate that CD9 and CD81 have an important role in membrane fusion induced by HIV-1 envelope.

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