干扰素
RNA沉默
干扰素调节因子
Toll样受体
TLR4型
生物
脂多糖
先天免疫系统
促炎细胞因子
细胞生物学
转录因子
趋化因子
信号转导
受体
微生物学
核糖核酸
免疫学
基因
炎症
RNA干扰
遗传学
作者
Noriaki Shinobu,Tomokatsu Iwamura,Mitsutoshi Yoneyama,Kazumi Yamaguchi,Wakako Suhara,Yukiko Fukuhara,Fumio Amano,Takashi Fujita
出处
期刊:FEBS Letters
[Wiley]
日期:2002-04-05
卷期号:517 (1-3): 251-256
被引量:48
标识
DOI:10.1016/s0014-5793(02)02636-4
摘要
Infections of bacteria and viruses induce host defense reactions known as innate responses that include the production of cytokines and chemokines. The production of type I interferon (IFN) is known to be induced by viral double‐stranded (ds) RNA or bacterial lipopolysaccharide (LPS). Although important functions for the transcription factors NF‐κB and interferon regulatory factor‐3 (IRF‐3) are indicated, the molecular signals leading to the activation of IFN genes have yet to be elucidated. We provide several lines of evidence that LPS and dsRNA trigger distinct intracellular signals upstream. Notably, our investigation revealed a critical function for TIRAP/MAL, a signaling adapter for Toll‐like receptor (TLR) 4, in LPS‐induced but not dsRNA‐induced activation of IRF‐3. These results highlight cross‐talk between TLR‐mediated and virus/dsRNA‐induced signals resulting in activation of the IFN system.
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