IKKε and TBK1 are essential components of the IRF3 signaling pathway

被引:2243
作者
Fitzgerald, KA
McWhirter, SM
Faia, KL
Rowe, DC
Latz, E
Golenbock, DT
Coyle, AJ
Liao, SM
Maniatis, T [1 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[2] Univ Massachusetts, Div Infect Dis & Immunol, Worcester, MA 01605 USA
[3] Millennium Pharmaceut Inc, Dept Inflammat, Cambridge, MA 02139 USA
关键词
D O I
10.1038/ni921
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The transcription factors interferon regulatory factor 3 (IRF3) and NF-kappaB are required for the expression of many genes involved in the innate immune response. Viral infection, or the binding of double-stranded RNA to Toll-like receptor 3, results in the coordinate activation of IRF3 and NF-kappaB. Activation of IRF3 requires signal-dependent phosphorylation, but little is known about the signaling pathway or kinases involved. Here we report that the noncanonical lkappaB kinase homologs, IkappaB kinase-epsilon, (IKKepsilon) and TANK-binding kinase-I (TBK1), which were previously implicated in NF-kappaB activation, are also essential components of the IRF3 signaling pathway. Thus, IKKKepsilon and TBKI have a pivotal role in coordinating the activation of IRF3 and NF-kappaB in the innate immune response.
引用
收藏
页码:491 / 496
页数:6
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