...
首页> 外文期刊>Nature immunology >Interferon-alpha induction through Toll-like receptors involves a direct interaction of IRF7 with MyD88 and TRAF6.
【24h】

Interferon-alpha induction through Toll-like receptors involves a direct interaction of IRF7 with MyD88 and TRAF6.

机译:通过Toll样受体的干扰素α诱导涉及IRF7与MyD88和TRAF6的直接相互作用。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Toll-like receptors (TLRs) are involved in the recognition of microbial pathogens. A subset of TLRs, TLR7, TLR8 and TLR9, induces antiviral responses by producing interferon-alpha (IFN-alpha). Production of IFN-alpha is dependent on the Toll-interleukin-1 receptor domain-containing adaptor MyD88. Here we show that MyD88 formed a complex with the transcription factor IRF7 but not with IRF3. The death domain of MyD88 interacted with an inhibitory domain of IRF7, and this interaction resulted in activation of the IFN-alpha-dependent promoters. Furthermore, the adaptor molecule TRAF6 also bound and activated IRF7. Ubiquitin ligase activity of TRAF6 was required for IRF7 activation. These results indicate that TLR-mediated IFN-alpha induction requires the formation of a complex consisting of MyD88, TRAF6 and IRF7 as well as TRAF6-dependent ubiquitination.
机译:Toll样受体(TLR)参与微生物病原体的识别。 TLR的一个子集TLR7,TLR8和TLR9通过产生α-干扰素(IFN-α)诱导抗病毒反应。 IFN-α的产生取决于包含Toll-白介素1受体域的衔接子MyD88。在这里,我们显示MyD88与转录因子IRF7形成复合体,但与IRF3形成复合体。 MyD88的死亡域与IRF7的抑制域相互作用,并且这种相互作用导致IFN-α依赖性启动子的激活。此外,衔接子分子TRAF6也结合并激活了IRF7。激活IRF7需要TRAF6的泛素连接酶活性。这些结果表明,TLR介导的IFN-α诱导需要形成由MyD88,TRAF6和IRF7以及TRAF6依赖性泛素化组成的复合物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号