New frontiers in the cGAS-STING intracellular DNA-sensing pathway

被引:45
作者
Dvorkin, Steve [1 ,2 ]
Cambier, Stephanie [1 ,2 ]
Volkman, Hannah E. [1 ,2 ]
Stetson, Daniel B. [1 ,2 ]
机构
[1] Univ Washington, Sch Med, Dept Immunol, Seattle, WA 98109 USA
[2] Univ Washington, Sch Med, Dept Med, Seattle, WA 98109 USA
基金
美国国家科学基金会;
关键词
AICARDI-GOUTIERES SYNDROME; CYCLIC GMP-AMP; MITOCHONDRIAL-DNA; I INTERFERON; EXTRACELLULAR CGAMP; STRUCTURAL BASIS; CHROMATIN; ACTIVATION; MECHANISMS; RECOGNITION;
D O I
10.1016/j.immuni.2024.02.019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The cGAS-STING intracellular DNA-sensing pathway has emerged as a key element of innate antiviral immunity and a promising therapeutic target. The existence of an innate immune sensor that can be activated by any double-stranded DNA (dsDNA) of any origin raises fundamental questions about how cGAS is regulated and how it responds to "foreign"DNA while maintaining tolerance to ubiquitous self-DNA. In this review, we summarize recent evidence implicating important roles for cGAS in the detection of foreign and self-DNA. We describe two recent and surprising insights into cGAS-STING biology: that cGAS is tightly tethered to the nucleosome and that the cGAMP product of cGAS is an immunotransmitter acting at a distance to control innate immunity. We consider how these advances influence our understanding of the emerging roles of cGAS in the DNA damage response (DDR), senescence, aging, and cancer biology. Finally, we describe emerging approaches to harness cGAS-STING biology for therapeutic benefit.
引用
收藏
页码:718 / 730
页数:13
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