RACK1与STING相关,以促进I型干扰素激活,并抑制伪狂热病毒感染
Yixuan Li1, Yiyu Liu1, Yu Dai1
1Joint International Research Laboratory of Animal Health and Animal Food Safety, College of Veterinary Medicine, Southwest University, Chongqing, 400715, China, swu.edu.cn.
Transboundary and emerging diseases
|December 15, 2025
概括
活性蛋白激酶C 1 (RACK1) 的受体通过增强I型干扰素 (IFN-I) 信号传递来抑制伪狂犬病病毒 (PRV) 复制. RACK1与STING相互作用,促进IFN-I激活,并限制猪细胞中的PRV感染.
科学领域:
- 病毒学 病毒学
- 免疫学 免疫学 免疫学
- 细胞生物学 细胞生物学
背景情况:
- 伪狂犬病病毒 (PRV) 在全球猪生产中造成重大经济损失.
- 活性蛋白激酶C 1 (RACK1) 的受体与各种病毒感染有关,但其在PRV中的作用尚不清楚.
研究的目的:
- 研究RACK1在PRV感染中的作用及其对宿主免疫反应的影响.
主要方法:
- 在猪-15 (PK-15) 细胞中感染PRV.
- 对RACK1,IFN-β,ISG15和ISG20表达水平的分析.
- 研究RACK1与STING和IRF3酸化的相互作用.
主要成果:
- 在受PRV感染的细胞中,RACK1表达与IFN-β,ISG15和ISG20正相关.
- RACK1抑制了PRV复制,并增强了I型干扰素 (IFN-I) 信号传输.
- RACK1促进了依赖STING的IRF3酸化,并与STING相互作用,促进其聚合.
结论:
- RACK1作为一种宿主因子,通过促进依赖STING的IFN-I激活来限制PRV感染.
- 这项研究增强了对RACK1的抗病毒机制和在PRV感染期间的IFN-I反应的理解.
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