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Inhibition Of Rig-i And Mda5-dependent Antiviral Response By Gc1qr At Mitochondria

机译:Gc1qr在线粒体抑制Rig-i和Mda5依赖性抗病毒反应

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摘要

gC1qR is one of the C1q receptors implicated in the regulation of innate and adaptive immunity. We found that gC1qR inhibits RIG-I and MDA5-dependent antiviral signaling. Double stranded RNA and virus trigger the translocation of gC1qR to the mitochondrial outer membrane leading to the interaction of gC1qR with the RIG-I and MDA5 adaptor, VISA/MAVS/IPS-1/Cardif. The interaction of gC1qR with VISA/MAVS/IPS-1/Cardif at mitochondria results in the disruption of RIG-I and MDA5 signaling and the promotion of virus replication. Knockdown of endogenous gC1qR enhances RIG-I-dependent antiviral signaling, and augments the inhibition of virus proliferation. Therefore, gC1qR is a physiological inhibitor of the RIG-I and MDA5-mediated antiviral signaling pathway. These data uncover a new viral mechanism used to negatively control antiviral signaling in host cells.
机译:gC1qR是C1q受体之一,涉及先天和适应性免疫的调节。我们发现gC1qR抑制RIG-1和MDA5依赖性抗病毒信号传导。双链RNA和病毒触发gC1qR易位至线粒体外膜,从而导致gC1qR与RIG-1和MDA5衔接子VISA / MAVS / IPS-1 / Cardif相互作用。 gC1qR与VISA / MAVS / IPS-1 / Cardif在线粒体上的相互作用导致RIG-1和MDA5信号的破坏,并促进了病毒复制。内源性gC1qR的组合可增强RIG-I依赖的抗病毒信号传导,并增强对病毒增殖的抑制作用。因此,gC1qR是RIG-1和MDA5介导的抗病毒信号通路的生理抑制剂。这些数据揭示了一种新的病毒机制,用于负控制宿主细胞中的抗病毒信号。

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