Structure, Activation and Regulation of NLRP3 and AIM2 Inflammasomes

被引:113
|
作者
Sharma, Meenakshi [1 ]
de Alba, Eva [1 ]
机构
[1] Univ Calif Merced, Sch Engn, Dept Bioengn, 5200 North Lake Rd, Merced, CA 95343 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
inflammation; ASC (apoptosis-associated speck-like protein containing a CARD); NLRP3; AIM2; NMR; protein structure; protein assembly; NF-KAPPA-B; MULTISYSTEM INFLAMMATORY DISEASE; RECEPTOR-INTERACTING PROTEIN-2; INTERFERON-INDUCIBLE PROTEIN; RECRUITMENT DOMAIN PROTEIN; ASC PYRIN DOMAIN; CRYSTAL-STRUCTURE; CUTTING EDGE; CELL-DEATH; NALP3; INFLAMMASOME;
D O I
10.3390/ijms22020872
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
The inflammasome is a three-component (sensor, adaptor, and effector) filamentous signaling platform that shields from multiple pathogenic infections by stimulating the proteolytical maturation of proinflammatory cytokines and pyroptotic cell death. The signaling process initiates with the detection of endogenous and/or external danger signals by specific sensors, followed by the nucleation and polymerization from sensor to downstream adaptor and then to the effector, caspase-1. Aberrant activation of inflammasomes promotes autoinflammatory diseases, cancer, neurodegeneration, and cardiometabolic disorders. Therefore, an equitable level of regulation is required to maintain the equilibrium between inflammasome activation and inhibition. Recent advancement in the structural and mechanistic understanding of inflammasome assembly potentiates the emergence of novel therapeutics against inflammasome-regulated diseases. In this review, we have comprehensively discussed the recent and updated insights into the structure of inflammasome components, their activation, interaction, mechanism of regulation, and finally, the formation of densely packed filamentous inflammasome complex that exists as micron-sized punctum in the cells and mediates the immune responses.
引用
收藏
页码:1 / 37
页数:37
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