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Phase separation in cGAS-STING signaling
被引:7
|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.
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页码:855 / 866
页数:12
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