An emerging role for calcium signalling in innate and autoimmunity via the cGAS-STING axis

被引:40
作者
Mathavarajah, Sabateeshan [1 ]
Salsman, Jayme [1 ]
Dellaire, Graham [1 ,2 ]
机构
[1] Dalhousie Univ, Fac Med, Dept Pathol, Halifax, NS, Canada
[2] Dalhousie Univ, Dept Biochem & Mol Biol, Halifax, NS, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
STING; SLE; TREX1; cGAS; Calcium signalling; Innate immunity; Type I interferon response; GMP-AMP SYNTHASE; I INTERFERONS; MITOCHONDRIAL-DNA; KINASE IV; IMMUNE; AUTOPHAGY; TREX1; PHOSPHORYLATION; RECOGNITION; INFECTION;
D O I
10.1016/j.cytogfr.2019.04.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Type I interferons are effector cytokines essential for the regulation of the innate immunity. A key effector of the type I interferon response that is dysregulated in autoimmunity and cancer is the cGAS-STING signalling axis. Recent work suggests that calcium and associated signalling proteins can regulate both cGAS-STING and autoimmunity. How calcium regulates STING activation is complex and involves both stimulatory and inhibitory mechanisms. One of these is calmodulin-mediated signalling that is necessary for STING activation. The alterations in calcium flux that occur during STING activation can also regulate autophagy, which in turn plays a role in innate immunity through the clearance of intracellular pathogens. Also connected to calcium signalling pathways is the cGAS inhibitor TREX1, a cytoplasmic exonuclease linked to several autoimmune diseases including systemic lupus erythematosus (SLE). In this review, we summarize these and other findings that indicate a regulatory role for calcium signalling in innate and autoimmunity through the cGAS-STING pathway.
引用
收藏
页码:43 / 51
页数:9
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