Author/Authors :
Jun Cui، نويسنده , , Liang Zhu، نويسنده , , Xiaojun Xia، نويسنده , , Helen Y. Wang، نويسنده , , Xavier Legras، نويسنده , , Jun Hong، نويسنده , , Jiabing Ji، نويسنده , , Pingping Shen، نويسنده , , Shu Zheng، نويسنده , , Zhijian J. Chen، نويسنده , , Rong-Fu Wang، نويسنده ,
Abstract :
Stringent control of the NF-κB 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-κB-dependent responses by interacting with IKKα and IKKβ 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-κB and its responsive genes, TNF-α 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-κB and type I interferon signaling pathways and suggest an important role for NLRC5 in homeostatic control of innate immunity.