首页> 外文期刊>Immunity >Antiviral protein Viperin promotes Toll-like receptor 7- and Toll-like receptor 9-mediated type I interferon production in plasmacytoid dendritic cells.
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Antiviral protein Viperin promotes Toll-like receptor 7- and Toll-like receptor 9-mediated type I interferon production in plasmacytoid dendritic cells.

机译:抗病毒蛋白毒蛇毒素可促进浆细胞样树突状细胞中Toll样受体7和Toll样受体9介导的I型干扰素产生。

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摘要

Toll-like receptor 7 (TLR7) and TLR9 sense viral nucleic acids and induce production of type I interferon (IFN) by plasmacytoid dendritic cells (pDCs) to protect the host from virus infection. We showed that the IFN-inducible antiviral protein Viperin promoted TLR7- and TLR9-mediated production of type I IFN by pDCs. Viperin expression was potently induced after TLR7 or TLR9 stimulation and Viperin localized to the cytoplasmic lipid-enriched compartments, lipid bodies, in pDCs. Viperin interacted with the signal mediators IRAK1 and TRAF6 to recruit them to the lipid bodies and facilitated K63-linked ubiquitination of IRAK1 to induce the nuclear translocation of transcription factor IRF7. Loss of Viperin reduced TLR7- and TLR9-mediated production of type I IFN by pDCs. However, Viperin was dispensable for the production of type I IFN induced by intracellular nucleic acids. Thus, Viperin mediates its antiviral function via the regulation of the TLR7 and TLR9-IRAK1 signaling axis in pDCs.
机译:Toll样受体7(TLR7)和TLR9感应病毒核酸并诱导浆细胞样树突状细胞(pDC)产生I型干扰素(IFN),以保护宿主免受病毒感染。我们显示,IFN诱导型抗病毒蛋白毒蛇毒素可促进pDCs的TLR7和TLR9介导的I型IFN的产生。在TLR7或TLR9刺激后,Viperin的表达被有效诱导,Viperin定位于pDC中细胞质富含脂质的区室,脂质体。毒蛇毒蛋白与信号介质IRAK1和TRAF6相互作用,将它们募集到脂质体上,并促进IRAK1的K63连接泛素化,以诱导转录因子IRF7的核易位。失去Viperin减少了pDCs的TLR7和TLR9介导的I型IFN产生。然而,Viperin对于细胞内核酸诱导的I型IFN的产生是必不可少的。因此,Viperin通过调节pDC中的TLR7和TLR9-IRAK1信号轴来介导其抗病毒功能。

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