坦克结合激酶1
激酶
IκB激酶
生物
干扰素
磷酸化
信号转导
细胞生物学
RNA沉默
Toll样受体
干扰素调节因子
分子生物学
病毒学
NF-κB
基因
先天免疫系统
核糖核酸
MAP激酶激酶激酶
RNA干扰
蛋白激酶A
免疫系统
免疫学
生物化学
作者
Hiroaki Hemmi,Osamu Takeuchi,Shintaro Sato,Masahiro Yamamoto,Tsuneyasu Kaisho,Hideki Sanjo,Taro Kawai,Katsuaki Hoshino,Kiyoshi Takeda,Shizuo Akira
摘要
Viral infection and stimulation with lipopolysaccharide (LPS) or double stranded RNA (dsRNA) induce phosphorylation of interferon (IFN) regulatory factor (IRF)-3 and its translocation to the nucleus, thereby leading to the IFN-β gene induction. Recently, two IκB kinase (IKK)–related kinases, inducible IκB kinase (IKK-i) and TANK-binding kinase 1 (TBK1), were suggested to act as IRF-3 kinases and be involved in IFN-β production in Toll-like receptor (TLR) signaling and viral infection. In this work, we investigated the physiological roles of these kinases by gene targeting. TBK1-deficient embryonic fibroblasts (EFs) showed dramatic decrease in induction of IFN-β and IFN-inducible genes in response to LPS or dsRNA as well as after viral infection. However, dsRNA-induced expression of these genes was residually detected in TBK1-deficient cells and intact in IKK-i–deficient cells, but completely abolished in IKK-i/TBK1 doubly deficient cells. IRF-3 activation, in response not only to dsRNA but also to viral infection, was impaired in TBK1-deficient cells. Together, these results demonstrate that TBK1 as well as, albeit to a lesser extent, IKK-i play a crucial role in the induction of IFN-β and IFN-inducible genes in both TLR-stimulated and virus-infected EFs.
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