JNK regulates the release of proapoptotic mitochondrial factors in reovirus-infected cells

被引:53
|
作者
Clarke, P
Meintzer, SM
Wang, YB
Moffitt, LA
Richardson-Burns, SM
Johnson, GL
Tyler, KL
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Neurol B182, Denver, CO 80262 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Immunol, Denver, CO 80262 USA
[3] Univ Colorado, Hlth Sci Ctr, Dept Neurosci, Denver, CO 80262 USA
[4] Univ Colorado, Hlth Sci Ctr, Dept Med & Microbiol, Denver, CO 80262 USA
[5] Denver Vet Affairs Med Ctr, Denver, CO USA
[6] Univ N Carolina, Sch Med, Dept Pharmacol, Chapel Hill, NC USA
[7] Univ N Carolina, Lineberger Comprehens Canc Ctr, Sch Med, Chapel Hill, NC 27599 USA
关键词
D O I
10.1128/JVI.78.23.13132-13138.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Reovirus-induced apoptosis is associated with activation of the proapoptotic mitogen-activated protein kinase c-Jun N-terminal kinase (JNK) and the JNK-associated transcription factor c-Jun. Here we show that reovirus-induced apoptosis and activation of caspase 3 are inhibited in cells deficient in MEK kinase 1, an upstream activator of JNK in reovirus-infected cells. Inhibition of JNK activity following reovirus infection delays the release of proapoptotic mitochondrial factors and the subsequent onset of apoptosis. In contrast, reovirus-induced apoptosis is not blocked by infection with adenovirus expressing dominant-negative c-Jun, and c-Jun activation does not correlate with apoptosis in reovirus-infected cells. This is the first report demonstrating that JNK is associated with regulation of mitochondrial pathways of apoptosis following viral infection.
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页码:13132 / 13138
页数:7
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