Abstract
Feline immunodeficiency virus (FIV) induces a disease similar to acquired immunodeficiency syndrome (AIDS) in cats, yet in contrast to human immunodeficiency virus (HIV), CD4 is not the viral receptor. We identified a primary receptor for FIV as CD134 (OX40), a T cell activation antigen and costimulatory molecule. CD134 expression promotes viral binding and renders cells permissive for viral entry, productive infection, and syncytium formation. Infection is CXCR4-dependent, analogous to infection with X4 strains of HIV. Thus, despite the evolutionary divergence of the feline and human lentiviruses, both viruses use receptors that target the virus to a subset of cells that are pivotal to the acquired immune response.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Amino Acid Sequence
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Animals
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Benzylamines
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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 / virology
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Cats
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Cell Line
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Cell Line, Tumor
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Cyclams
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DNA, Complementary
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Gene Library
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HIV / metabolism
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HeLa Cells
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Heterocyclic Compounds / pharmacology
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Humans
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Immunodeficiency Virus, Feline / metabolism*
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Immunodeficiency Virus, Feline / pathogenicity
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Mice
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Molecular Sequence Data
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NIH 3T3 Cells
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Receptors, CXCR4 / antagonists & inhibitors
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Receptors, CXCR4 / metabolism
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Receptors, OX40
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Receptors, Tumor Necrosis Factor / chemistry
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Receptors, Tumor Necrosis Factor / genetics
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Receptors, Tumor Necrosis Factor / immunology
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Receptors, Tumor Necrosis Factor / metabolism*
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Receptors, Virus / chemistry
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Receptors, Virus / genetics
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Receptors, Virus / immunology
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Receptors, Virus / metabolism*
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Species Specificity
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Transduction, Genetic
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Transfection
Substances
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Benzylamines
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Cyclams
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DNA, Complementary
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Heterocyclic Compounds
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Receptors, CXCR4
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Receptors, OX40
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Receptors, Tumor Necrosis Factor
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Receptors, Virus
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TNFRSF4 protein, human
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Tnfrsf4 protein, mouse
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plerixafor