Activation and evasion of inflammasomes during viral and microbial infection

被引:0
|
作者
Ren, Dan [1 ]
Ye, Xiaoou [1 ]
Chen, Ruiming [1 ]
Jia, Xiuzhi [1 ]
He, Xianhong [1 ]
Tao, Jinhui [2 ]
Jin, Tengchuan [1 ,3 ]
Wu, Songquan [1 ]
Zhang, Hongliang [1 ]
机构
[1] Lishui Univ, Coll Med, Ctr Dis Immun & Intervent, Lishui 323000, Peoples R China
[2] Univ Sci & Technol China, Affiliated Hosp 1, Dept Rheumatol & Immunol, Div Life Sci & Med,USTC, Hefei 230001, Peoples R China
[3] Univ Sci & Technol China, Div Life Sci & Med, Lab Struct Immunol, CAS Key Lab Innate Immun & Chron Dis, Hefei 230001, Peoples R China
基金
中国国家自然科学基金;
关键词
Inflammasome; NLRP3; AIM2; Viral; Microbe; Evasion; NLRP3; INFLAMMASOME; AIM2; INFLUENZA-VIRUS; PORPHYROMONAS-GINGIVALIS; CASPASE-1; ACTIVATION; IL-1-BETA PRODUCTION; SUBTILASE CYTOTOXIN; HOST-DEFENSE; GASDERMIN D; CELL-DEATH;
D O I
10.1007/s00018-025-05575-2
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 cytoplasmic multiprotein complex that induces the maturation of the proinflammatory cytokines interleukin-1 beta (IL-1 beta) and interleukin-18 (IL-18) or pyroptosis by activating caspases, which play critical roles in regulating inflammation, cell death, and various cellular processes. Multiple studies have shown that the inflammasome is a key regulator of the host defence response against pathogen infections. During the process of pathogenic microbe invasion into host cells, the host's innate immune system recognizes these microbes by activating inflammasomes, triggering inflammatory responses to clear the microbes and initiate immune responses. Moreover, microbial pathogens have evolved various mechanisms to inhibit or evade the activation of inflammasomes. Therefore, we review the interactions between viruses and microbes with inflammasomes during the invasion process, highlight the molecular mechanisms of inflammasome activation induced by microbial pathogen infection, and highlight the corresponding strategies that pathogens employ to evade inflammasome activity. Finally, we also discuss potential therapeutic strategies for the treatment of pathogenic microbial infections via the targeting of inflammasomes and their products.
引用
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页数:16
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