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
A JC virus-induced signal is required for infection of glial cells by a clathrin- and eps15-dependent pathway / W. Querbes, A. Benmerah, D. Tosoni, P.P. Di Fiore, W.J. Atwood. - In: JOURNAL OF VIROLOGY. - ISSN 0022-538X. - 78:1(2004 Jan), pp. 250-256.
A JC virus-induced signal is required for infection of glial cells by a clathrin- and eps15-dependent pathway
D. Tosoni;P.P. Di FiorePenultimo
;
2004
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 mechanismPubblicazioni consigliate
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