NLRC5 Negatively Regulates the NF-κB and Type I Interferon Signaling Pathways

被引:394
作者
Cui, Jun [1 ,2 ,3 ]
Zhu, Liang [1 ,2 ,4 ]
Xia, Xiaojun [1 ,2 ]
Wang, Helen Y. [1 ,2 ]
Legras, Xavier [1 ,2 ]
Hong, Jun [1 ,2 ]
Ji, Jiabing [1 ,2 ]
Shen, Pingping [3 ]
Zheng, Shu [4 ]
Chen, Zhijian J. [5 ]
Wang, Rong-Fu [1 ,2 ]
机构
[1] Baylor Coll Med, Ctr Cell & Gene Therapy, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Pathol & Immunol, Houston, TX 77030 USA
[3] Nanjing Univ, Coll Life Sci, Nanjing 210008, Peoples R China
[4] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Inst Canc, Hangzhou 310003, Zhejiang, Peoples R China
[5] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Howard Hughes Med Inst, Dallas, TX 75390 USA
关键词
PATTERN-RECOGNITION RECEPTORS; RIG-I; TOLL-LIKE; INNATE IMMUNITY; T-CELLS; INFLAMMATORY DISEASE; NALP3; INFLAMMASOME; UBIQUITIN LIGASE; KINASE COMPLEX; RNA;
D O I
10.1016/j.cell.2010.03.040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Stringent control of the NF-kappa B and type I interferon signaling pathways is critical to effective host immune responses, yet the molecular mechanisms that negatively regulate these pathways are poorly understood. Here, we show that NLRC5, a member of the highly conserved NOD-like protein family, can inhibit the IKK complex and RIG-I/MDA5 function. NLRC5 inhibited NF-kappa B-dependent responses by interacting with IKK alpha and IKK beta and blocking their phosphorylation. It also interacted with RIG-I and MDA5, but not with MAVS, to inhibit RLR-mediated type I interferon responses. Consistent with these observations, NLRC5-specific siRNA knockdown not only enhanced the activation of NF-kappa B and its responsive genes, TNF-alpha and IL-6, but also promoted type I interferon signaling and antiviral immunity. Our findings identify NLRC5 as a negative regulator that blocks two central components of the NF-kappa B and type I interferon signaling pathways and suggest an important role for NLRC5 in homeostatic control of innate immunity.
引用
收藏
页码:483 / 496
页数:14
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