Induction of interleukin-6 after stimulation of human B-cell CD21 by Epstein-Barr virus glycoproteins gp350 and gp220

被引:44
|
作者
Tanner, JE
Alfieri, C
Chatila, TA
DiazMitoma, F
机构
[1] UNIV OTTAWA,OTTAWA,ON K1H 8L1,CANADA
[2] HOP ST JUSTINE,PEDIAT RES CTR,MOLEC VIROL LAB,MONTREAL,PQ H3T 1C5,CANADA
[3] WASHINGTON UNIV,DEPT PEDIAT,DIV IMMUNOL,ST LOUIS,MO 63110
关键词
D O I
10.1128/JVI.70.1.570-575.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:570 / 575
页数:6
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