内部收益率3
干扰素调节因子
IκB激酶
坦克结合激酶1
信号转导
激酶
转录因子
细胞生物学
生物
先天免疫系统
磷酸化
免疫系统
NF-κB
免疫学
基因
蛋白激酶A
MAP激酶激酶激酶
遗传学
作者
Katherine A. Fitzgerald,Sarah M. McWhirter,L. Kerrie,Daniel C. Rowe,Eicke Latz,Douglas T. Golenbock,Anthony J. Coyle,Sha-Mei Liao,Tom Maniatis
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 IkappaB kinase homologs, IkappaB kinase-epsilon (IKKepsilon) and TANK-binding kinase-1 (TBK1), which were previously implicated in NF-kappaB activation, are also essential components of the IRF3 signaling pathway. Thus, IKKepsilon and TBK1 have a pivotal role in coordinating the activation of IRF3 and NF-kappaB in the innate immune response.
科研通智能强力驱动
Strongly Powered by AbleSci AI