Abstract
Infectious entry of JC virus (JCV) into human glial cells occurs by receptor-mediated clathrin-dependent endocytosis. In this report we demonstrate that the tyrosine kinase inhibitor genistein blocks virus entry and inhibits infection. Transient expression of dominant-negative eps15 mutants, including a phosphorylation-defective mutant, inhibited both virus entry and infection. We also show that the JCV-induced signal activates the mitogen-activated protein kinases ERK1 and ERK2. These data demonstrate that JC virus binding to human glial cells induces an intracellular signal that is critical for entry and infection by a ligand-inducible clathrin-dependent mechanism.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adaptor Proteins, Signal Transducing
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Calcium-Binding Proteins / genetics
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Calcium-Binding Proteins / metabolism*
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Clathrin / metabolism*
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Humans
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Intracellular Signaling Peptides and Proteins
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Isoflavones / pharmacology
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JC Virus / pathogenicity*
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Mitogen-Activated Protein Kinase 1 / genetics
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Mitogen-Activated Protein Kinase 1 / metabolism
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Mitogen-Activated Protein Kinase 3
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Mitogen-Activated Protein Kinases / genetics
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Mitogen-Activated Protein Kinases / metabolism
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Mutation
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Neuroglia / virology*
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Phosphoproteins / genetics
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Phosphoproteins / metabolism*
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Signal Transduction*
Substances
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Adaptor Proteins, Signal Transducing
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Calcium-Binding Proteins
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Clathrin
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EPS15 protein, human
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Intracellular Signaling Peptides and Proteins
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Isoflavones
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Phosphoproteins
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genistin
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Mitogen-Activated Protein Kinase 1
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Mitogen-Activated Protein Kinase 3
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Mitogen-Activated Protein Kinases