炎症体
线粒体
生物
线粒体DNA
细胞生物学
电压依赖性阴离子通道
胞浆
线粒体ROS
生物化学
细菌外膜
基因
酶
受体
大肠杆菌
作者
Hongxu Xian,Kosuke Watari,Elsa Sánchez‐López,Joseph Offenberger,Janset Onyuru,Harini Sampath,Wei Ying,Hal M. Hoffman,Gerald S. Shadel,Michael Karin
出处
期刊:Immunity
[Elsevier]
日期:2022-07-13
卷期号:55 (8): 1370-1385.e8
被引量:293
标识
DOI:10.1016/j.immuni.2022.06.007
摘要
Mitochondrial DNA (mtDNA) escaping stressed mitochondria provokes inflammation via cGAS-STING pathway activation and, when oxidized (Ox-mtDNA), it binds cytosolic NLRP3, thereby triggering inflammasome activation. However, it is unknown how and in which form Ox-mtDNA exits stressed mitochondria in non-apoptotic macrophages. We found that diverse NLRP3 inflammasome activators rapidly stimulated uniporter-mediated calcium uptake to open mitochondrial permeability transition pores (mPTP) and trigger VDAC oligomerization. This occurred independently of mtDNA or reactive oxygen species, which induce Ox-mtDNA generation. Within mitochondria, Ox-mtDNA was either repaired by DNA glycosylase OGG1 or cleaved by the endonuclease FEN1 to 500–650 bp fragments that exited mitochondria via mPTP- and VDAC-dependent channels to initiate cytosolic NLRP3 inflammasome activation. Ox-mtDNA fragments also activated cGAS-STING signaling and gave rise to pro-inflammatory extracellular DNA. Understanding this process will advance the development of potential treatments for chronic inflammatory diseases, exemplified by FEN1 inhibitors that suppressed interleukin-1β (IL-1β) production and mtDNA release in mice.
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