Noncanonical NF-κB Pathway Controls the Production of Type I Interferons in Antiviral Innate Immunity

被引:108
|
作者
Jin, Jin [1 ]
Hu, Hongbo [1 ]
Li, Haiyan S. [1 ]
Yu, Jiayi [1 ]
Xiao, Yichuan [1 ]
Brittain, George C. [1 ]
Zou, Qiang [1 ]
Cheng, Xuhong [1 ]
Mallette, Frederick A. [2 ]
Watowich, Stephanie S. [1 ,3 ]
Sun, Shao-Cong [1 ,3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
[2] Univ Montreal, Dept Med, Montreal, PQ H1T 2M4, Canada
[3] Univ Texas Grad Sch Biomed Sci Houston, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
GENE-EXPRESSION; IFN-BETA; KINASE; ACTIVATION; ALPHA; TRAF3; INDUCTION; COMPLEX; UBIQUITINATION; METHYLATION;
D O I
10.1016/j.immuni.2014.02.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Production of type I interferons (IFN-I) is a crucial innate immune mechanism against viral infections. IFN-I induction is subject to negative regulation by both viral and cellular factors, but the underlying mechanism remains unclear. We report that the noncanonical NF-kappa B pathway was stimulated along with innate immune cell differentiation and viral infections and had a vital role in negatively regulating IFN-I induction. Genetic deficiencies in major components of the noncanonical NF-kappa B pathway caused IFN-I hyperinduction and rendered cells and mice substantially more resistant to viral infection. Noncanonical NF-kappa B suppressed signal-induced histone modifications at the Ifnb promoter, an action that involved attenuated recruitment of the transcription factor RelA and a histone demethylase, JMJD2A. These findings reveal an unexpected function of the noncanonical NF-kappa B pathway and highlight an important mechanism regulating antiviral innate immunity.
引用
收藏
页码:342 / 354
页数:13
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