Reovirus-induced apoptosis is mediated by TRAIL

被引:168
作者
Clarke, P
Meintzer, SM
Gibson, S
Widmann, C
Garrington, TP
Johnson, GL
Tyler, KL
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Neurol, Denver, CO 80262 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Pharmacol, Denver, CO 80262 USA
[3] Univ Colorado, Hlth Sci Ctr, Dept Med Microbiol & Immunol, Denver, CO 80262 USA
[4] Denver Vet Affairs Med Ctr, Denver, CO 80262 USA
[5] Natl Jewish Ctr Immunol & Resp Med, Program Mol Signal Transduct, Denver, CO 80206 USA
[6] Natl Jewish Ctr Immunol & Resp Med, Div Basic Sci, Denver, CO 80206 USA
关键词
D O I
10.1128/JVI.74.17.8135-8139.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Members of the tumor necrosis factor (TNF) receptor superfamily and their activating ligands transmit apoptotic signals in a variety of systems. We now show that the binding of TNF-related, apoptosis-inducing ligand (TRAIL) to its cellular receptors DR5 (TRAILR2) and DR4 (TRAILR1) mediates reovirus-induced apoptosis. Anti-TRAIL antibody and soluble TRAIL receptors block reovirus-induced apoptosis by preventing TRAIL-receptor binding. In addition, reovirus induces both TRAIL release and an increase in the expression of DR5 and DR4 in infected cells. Reovirus-induced apoptosis is also blocked following inhibition of the death receptor-associated, apoptosis-inducing molecules FADD (for LAS-associated death domain) and caspase 8. We propose that reovirus infection promotes apoptosis via the expression of DR5 and the release of TRAIL from infected cells. Virus-induced regulation of the TRAIL apoptotic pathway defines a novel mechanism for virus-induced apoptosis.
引用
收藏
页码:8135 / 8139
页数:5
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