IRF7
TLR7型
TLR9型
调节器
细胞生物学
干扰素
主调节器
化学
生物
受体
Toll样受体
先天免疫系统
免疫学
生物化学
基因
基因表达
DNA甲基化
转录因子
作者
Yanming Wang,Shanshan Yan,Bo Yang,Yan Wang,Haiyan Zhou,Qiaoshi Lian,Bing Sun
出处
期刊:FEBS Letters
[Wiley]
日期:2015-04-20
卷期号:589 (12): 1322-1330
被引量:32
标识
DOI:10.1016/j.febslet.2015.04.019
摘要
Toll‐like receptor 7 (TLR7) and TLR9 sense viral nucleic acids and induce type I IFN production, which must be properly controlled to avoid autoimmune diseases. Here, we report the negative regulation of TLR7/9‐mediated type I IFN production by TRIM35. TRIM35 expression is induced by TLR7/9 stimulation and then interacts with IRF7, which is the master regulator of type I IFN response. Furthermore, TRIM35 promotes the K48‐linked ubiquitination of IRF7 and induces its degradation via a proteasome‐dependent pathway. Therefore, TRIM35 is a negative feedback regulator of TLR7/9‐mediated type I IFN production due to its ability to suppress the stability of IRF7.
科研通智能强力驱动
Strongly Powered by AbleSci AI