Phase separation in cGAS-STING signaling

被引:8
作者
Li, Quanjin [1 ,2 ]
Gao, Pu [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Biophys, CAS Ctr Excellence Biomacromol, CAS Key Lab Infect & Immun,Natl Lab Biomacromol, Beijing 100101, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
biomolecular condensates; phase separation; cGAS-STING pathway; cGAS; STING; cGAMP; interferon; CYCLIC GMP-AMP; DOUBLE-STRANDED DNA; CELL-FREE FORMATION; TRANSCRIPTION FACTOR; CRYSTAL-STRUCTURE; ACTIVATION; BINDING; PROTEIN; IRF-3; 2ND-MESSENGER;
D O I
10.1007/s11684-023-1026-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Biomolecular condensates formed by phase separation are widespread and play critical roles in many physiological and pathological processes. cGAS-STING signaling functions to detect aberrant DNA signals to initiate anti-infection defense and antitumor immunity. At the same time, cGAS-STING signaling must be carefully regulated to maintain immune homeostasis. Interestingly, exciting recent studies have reported that biomolecular phase separation exists and plays important roles in different steps of cGAS-STING signaling, including cGAS condensates, STING condensates, and IRF3 condensates. In addition, several intracellular and extracellular factors have been proposed to modulate the condensates in cGAS-STING signaling. These studies reveal novel activation and regulation mechanisms of cGAS-STING signaling and provide new opportunities for drug discovery. Here, we summarize recent advances in the phase separation of cGAS-STING signaling and the development of potential drugs targeting these innate immune condensates.
引用
收藏
页码:855 / 866
页数:12
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