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首页> 外文期刊>The journal of immunology >Cutting Edge: Role of TANK-Binding Kinase 1 and Inducible IκB Kinase in IFN Responses against Viruses in Innate Immune Cells
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Cutting Edge: Role of TANK-Binding Kinase 1 and Inducible IκB Kinase in IFN Responses against Viruses in Innate Immune Cells

机译:前沿:TANK结合激酶1和诱导型IκB激酶在天然免疫细胞对病毒的IFN反应中的作用

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摘要

TANK-binding kinase 1 (TBK1) and inducible IκB kinase (IKK- i ) are involved in the activation of transcription factors inducing the production of type I IFNs. Although TBK1, but not IKK- i , is critical for LPS-induced IFN induction, the role of these kinases in the responses against viral infection is yet to be determined. In this study, we show that type I IFN production against various RNA viruses was completely abrogated in conventional dendritic cells (DCs) and macrophages induced from fetal liver cells lacking both TBK1 and IKK- i , whereas considerable amounts of IFN were produced in cells lacking either of them. Microarray analysis revealed that various IFN-inducible genes were also regulated by the kinases. In contrast, Fms-like tyrosine kinase 3 ligand-induced DCs produced IFN-α even in the absence of both TBK1 and IKK- i . Thus, these two kinases are essential and compensate each other for the regulation of IFN responses in innate immune cells except plasmacytoid DCs.
机译:TANK结合激酶1(TBK1)和诱导型IκB激酶(IKK-i)参与转录因子的激活,从而诱导I型IFN的产生。尽管TBK1而不是IKK-1对于LPS诱导的IFN诱导至关重要,但是这些激酶在抵抗病毒感染的反应中的作用尚待确定。在这项研究中,我们表明,针对传统的树突状细胞(DC)和缺乏TBK1和IKK-i的胎儿肝细胞诱导的巨噬细胞,针对各种RNA病毒的I型IFN产生已被完全废除,而缺乏TBK1和IKK-i的胎儿肝细胞诱导产生了大量的IFN。的任何一方。基因芯片分析显示,各种IFN诱导型基因也受激酶调节。相反,即使在没有TBK1和IKK-i的情况下,Fms样酪氨酸激酶3配体诱导的DC也会产生IFN-α。因此,这两种激酶是必不可少的,并且在除浆细胞样DC以外的先天免疫细胞中相互补偿,以调节IFN反应。

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