Abstract
HIV-1 Nef-mediated CD4 downmodulation involves various host factors. We investigated the importance of AP-1, AP-2, AP-3, V1H-ATPase, β-COP, and ACOT8 for CD4 downmodulation in HIV-1-infected short hairpin RNA (shRNA)-expressing CD4(+) T cells and characterized direct interaction with Nef by Förster resonance energy transfer (FRET). Binding of lentiviral Nefs to CD4 and AP-2 was conserved, and only AP-2 knockdown impaired Nef-mediated CD4 downmodulation from primary T cells. Altogether, among the factors tested, AP-2 is the most important player for Nef-mediated CD4 downmodulation.
Copyright © 2015, American Society for Microbiology. All Rights Reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adaptor Protein Complex 2 / genetics
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Adaptor Protein Complex 2 / immunology
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Adaptor Protein Complex 2 / metabolism*
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CD4 Antigens / biosynthesis*
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CD4 Antigens / genetics
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CD4 Antigens / immunology
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CD4-Positive T-Lymphocytes / immunology
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CD4-Positive T-Lymphocytes / metabolism*
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CD4-Positive T-Lymphocytes / pathology
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Down-Regulation*
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Gene Knockdown Techniques
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HIV Infections / genetics
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HIV Infections / immunology
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HIV Infections / metabolism*
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HIV Infections / pathology
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HIV-1 / genetics
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HIV-1 / immunology
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HIV-1 / metabolism*
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Humans
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nef Gene Products, Human Immunodeficiency Virus / genetics
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nef Gene Products, Human Immunodeficiency Virus / immunology
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nef Gene Products, Human Immunodeficiency Virus / metabolism*
Substances
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Adaptor Protein Complex 2
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CD4 Antigens
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nef Gene Products, Human Immunodeficiency Virus
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nef protein, Human immunodeficiency virus 1