Strategies of bacterial detection by inflammasomes

被引:1
|
作者
Jastrab, Jordan B. [1 ,2 ,3 ]
Kagan, Jonathan C. [1 ,2 ]
机构
[1] Boston Childrens Hosp, Div Gastroenterol, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Div Infect Dis, Boston, MA 02115 USA
关键词
INNATE IMMUNE RECOGNITION; OUTER-MEMBRANE VESICLES; AIM2; INFLAMMASOME; STAPHYLOCOCCUS-AUREUS; NLRP3; CUTTING EDGE; PATTERN-RECOGNITION; LISTERIA-MONOCYTOGENES; CASPASE-1; ACTIVATION; MYCOBACTERIUM-TUBERCULOSIS;
D O I
10.1016/j.chembiol.2024.03.009
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
Mammalian innate immunity is regulated by pattern -recognition receptors (PRRs) and guard proteins, which use distinct strategies to detect infections. PRRs detect bacterial molecules directly, whereas guards detect host cell manipulations by microbial virulence factors. Despite sensing infection through different mechanisms, both classes of innate immune sensors can activate the inflammasome, an immune complex that can mediate cell death and inflammation. Inflammasome-mediated immune responses are crucial for host defense against many bacterial pathogens and prevent invasion by non-pathogenic organisms. In this review, we discuss the mechanisms by which inflammasomes are stimulated by PRRs and guards during bacterial infection, and the strategies used by virulent bacteria to evade inflammasome-mediated immunity.
引用
收藏
页码:835 / 850
页数:16
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