抑制HIF因子通过IKKε的氧化来负面调节抗病毒先天免疫力
Xiaolian Cai1, Rui Wang2, Junji Zhu1
1Key Laboratory of Breeding Biotechnology and Sustainable Aquaculture, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, P.R. China.
Cell reports
|December 21, 2023
概括
抑制低氧诱导因子 (FIH) 抑制I型干扰素 (IFN-I) 信号通过化IκB激酶epsilon (IKKε). 缺乏FIH的模型显示对病毒感染的抗性增强,揭示了FIH在免疫力中的新作用.
科学领域:
- 免疫学 免疫学 免疫学
- 分子生物学分子生物学
- 病毒学 病毒学
背景情况:
- I型干扰素 (IFN-I) 信号传输对于抗病毒防御至关重要.
- 在病毒感染期间IκB激酶epsilon (IKKε) 激活的精确调节尚未完全理解.
研究的目的:
- 研究抑制缺氧诱导因子 (FIH) 在调节IKKε激活和随后的IFN-I信号传递中的作用.
- 阐明FIH控制IKKε活动的分子机制.
主要方法:
- 同免疫沉测试检测蛋白质相互作用.
- 质谱测量以确定IKKε上的基化位点.
- 使用缺乏FIH的小鼠和斑马鱼进行体内研究,以评估病毒耐药性.
主要成果:
- FIH与IKKε直接相互作用,并在Asn-254,Asn-700和Asn-701中氧化它.
- 通过FIH介导的基化抑制IKKε的激活,通过防止结合TBK1和TRAF3.
- 此外,FIH还可以抑制IKKε的K63结合的多比基化.
- 缺乏FIH的小鼠和斑马鱼对病毒感染的抵抗力增加.
结论:
- FIH充当IKKε激活的负调节器,从而抑制IFN-I信号传输.
- 这项研究揭示了FIH调节抗病毒免疫反应的新机制.
- 针对FIH-IKKε相互作用可以为病毒感染提供新的治疗策略.
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