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The cellular receptor for Epstein-Barr virus (EBV) is the type 2 complement receptor, CD21. At initial infection, EBV virion glycoproteins gp350 and gp220 bind to CD21. We report here that the cross-linking of CD21 by gp350/220 results in increased amounts of interleukin 6 (IL-6) RNA and IL-6 protein. This effect could be blocked with anti-gp350/220 and anti-CD21 monoclonal antibodies. Induction of IL-6 in B cells by EBV could be mimicked by treatment with the protein kinase C (PKC) activator phorbol 12,13-dibutyrate but not with the calcium ionophore ionomycin. IL-6 induction by EBV was inhibited with the PKC-specific inhibitor bisindolylmaleimide or the protein tyrosine kinase inhibitors methyl 2,5-dihydroxycinnamate and herbimycin A, indicating that the induction of IL-6 following CD21 cross-linking is mediated through PKC- and protein tyrosine kinase-dependent pathways.
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Jerome E. Tanner
Centre Hospitalier Universitaire Sainte-Justine
Caroline Alfieri
Centre Hospitalier Universitaire Sainte-Justine
Talal A. Chatila
Boston Children's Hospital
Journal of Virology
Children's Hospital of Eastern Ontario
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Tanner et al. (Mon,) studied this question.
synapsesocial.com/papers/6a1e12cf49e88a0d41608699 — DOI: https://doi.org/10.1128/jvi.70.1.570-575.1996