内部收益率3
IRF7
干扰素
干扰素调节因子
MDA5型
生物
基因敲除
钻机-I
细胞生物学
小干扰RNA
RNA解旋酶A
坦克结合激酶1
病毒学
先天免疫系统
内部收益率1
Ⅰ型干扰素
核糖核酸
转录因子
信号转导衔接蛋白
RNA干扰
免疫系统
信号转导
基因
激酶
解旋酶
免疫学
蛋白激酶A
遗传学
丝裂原活化蛋白激酶激酶
作者
Taro Kawai,Ken Takahashi,Shintaro Sato,Cevayir Coban,Himanshu Kumar,Hiroki Kato,Ken J. Ishii,Osamu Takeuchi,Shizuo Akira
摘要
Type I interferons are central mediators for antiviral responses. Using high-throughput functional screening of interferon inducers, we have identified here a molecule we call interferon-beta promoter stimulator 1 (IPS-1). Overexpression of IPS-1 induced type I interferon and interferon-inducible genes through activation of IRF3, IRF7 and NF-kappaB transcription factors. TBK1 and IKKi protein kinases were required for the IPS-1-mediated interferon induction. IPS-1 contained an N-terminal CARD-like structure that mediated interaction with the CARD of RIG-I and Mda5, which are cytoplasmic RNA helicases that sense viral infection. 'Knockdown' of IPS-1 by small interfering RNA blocked interferon induction by virus infection. Thus, IPS-1 is an adaptor involved in RIG-I- and Mda5-mediated antiviral immune responses.
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