多个未折叠蛋白质反应通路合作,将细胞质dDNA释放与干扰素基因刺激器 (STING) 激活联系起来
bioRxiv : the preprint server for biology
|May 27, 2024
概括
细胞内膜网膜应激激活了通过释放线粒体DNA来激活STING通路,涉及IRE1-XBP1和PERK等未折叠的蛋白质反应通路,即使没有直接的DNA刺激,也会导致IFN-β的产生.
科学领域:
- 免疫学 免疫学 免疫学
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
背景情况:
- 干扰素基因刺激器 (STING) 途径感知细胞质DNA,但其通过独立于直接DNA或循环二核酸的内源刺激的激活尚不清楚.
- 之前的研究将内等质网膜 (ER) 应激,特别是未折叠蛋白质反应 (UPR) 与STING激活联系起来.
结论:
- 多个UPR通路合作激活STING并诱导IFN-β,即使没有正规的STING或cGAS连接体.
- 包括病毒病原体在内的ER压力因素可以通过线粒体DNA的释放触发STING激活.
- 这种机制突出了先天免疫感应和对细胞压力和病毒感染的反应的新途径.
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