Activation and Pharmacological Regulation of Inflammasomes

被引:40
作者
Chen, Chen [1 ]
Xu, Pinglong [1 ,2 ]
机构
[1] Zhejiang Univ, Life Sci Inst, MOE Lab Biosyst Homeostasis & Protect, Zhejiang Prov Key Lab Canc Mol Cell Biol, Hangzhou 310058, Peoples R China
[2] Zhejiang Univ, Canc Ctr, Hangzhou 310058, Peoples R China
关键词
inflammasome; NLRP3; AIM2; caspase; IL-1; beta; GSDMD; inflammation; targeting; disease; inhibitor; INHIBITS NLRP3 INFLAMMASOME; NF-KAPPA-B; GASDERMIN-D; NALP3; INFLAMMASOME; K+ EFFLUX; IN-VIVO; AUTOINFLAMMATORY DISEASES; PATTERN-RECOGNITION; BACTERIAL LIGANDS; CELL BIOLOGY;
D O I
10.3390/biom12071005
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
Inflammasomes are intracellular signaling complexes of the innate immune system, which is part of the response to exogenous pathogens or physiological aberration. The multiprotein complexes mainly consist of sensor proteins, adaptors, and pro-caspase-1. The assembly of the inflammasome upon extracellular and intracellular cues drives the activation of caspase-1, which processes pro-inflammatory cytokines IL-1 beta and IL-18 to maturation and gasdermin-D for pore formation, leading to pyroptosis and cytokine release. Inflammasome signaling functions in numerous infectious or sterile inflammatory diseases, including inherited autoinflammatory diseases, metabolic disorders, cardiovascular diseases, cancers, neurodegenerative disorders, and COVID-19. In this review, we summarized current ideas on the organization and activation of inflammasomes, with details on the molecular mechanisms, regulations, and interventions. The recent developments of pharmacological strategies targeting inflammasomes as disease therapeutics were also covered.
引用
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页数:25
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