The cytosolic nucleic acid sensor LRRFIP1 mediates the production of type I interferon via a β-catenin-dependent pathway

被引:310
作者
Yang, Pengyuan [1 ,2 ]
An, Huazhang [1 ,2 ]
Liu, Xingguang [1 ,2 ]
Wen, Mingyue [1 ,2 ]
Zheng, Yuanyuan [1 ,2 ]
Rui, Yaocheng [1 ,2 ]
Cao, Xuetao [1 ,2 ]
机构
[1] Second Mil Med Univ, Natl Key Lab Med Immunol, Shanghai, Peoples R China
[2] Second Mil Med Univ, Inst Immunol, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
DOUBLE-STRANDED-RNA; INNATE IMMUNE-RESPONSES; LEUCINE-RICH REPEAT; RIG-I; TRANSCRIPTION FACTORS; DAI DLM-1/ZBP1; DNA; RECOGNITION; BINDING; ACTIVATION;
D O I
10.1038/ni.1876
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Intracellular nucleic acid sensors detect microbial RNA and DNA and trigger the production of type I interferon. However, the cytosolic nucleic acid-sensing system remains to be fully identified. Here we show that the cytosolic nucleic acid-binding protein LRRFIP1 contributed to the production of interferon-beta (IFN-beta) induced by vesicular stomatitis virus (VSV) and Listeria monocytogenes in macrophages. LRRFIP1 bound exogenous nucleic acids and increased the expression of IFN-beta induced by both double-stranded RNA and double-stranded DNA. LRRFIP1 interacted with beta-catenin and promoted the activation of beta-catenin, which increased IFN-beta expression by binding to the C-terminal domain of the transcription factor IRF3 and recruiting the acetyltransferase p300 to the IFN-beta enhanceosome via IRF3. Therefore, LRRFIP1 and its downstream partner beta-catenin constitute another coactivator pathway for IRF3-mediated production of type I interferon.
引用
收藏
页码:487 / U50
页数:9
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