Channelling inflammation: gasdermins in physiology and disease

被引:559
作者
Liu, Xing [1 ]
Xia, Shiyu [2 ,3 ]
Zhang, Zhibin [2 ,4 ]
Wu, Hao [2 ,3 ]
Lieberman, Judy [2 ,4 ]
机构
[1] Chinese Acad Sci, Ctr Microbes Dev & Hlth, Inst Pasteur Shanghai, Key Lab Mol Virol & Immunol, Shanghai, Peoples R China
[2] Boston Childrens Hosp, Program Cellular & Mol Med, Boston, MA 02115 USA
[3] Harvard Med Sch, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[4] Harvard Med Sch, Dept Pediat, Boston, MA 02115 USA
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
NONSYNDROMIC HEARING IMPAIRMENT; NEUTROPHIL EXTRACELLULAR TRAPS; DFNA5; GENE; GASTRIC-CANCER; HAIR FOLLICLE; GASTROINTESTINAL-TRACT; PROMOTER METHYLATION; MACROPHAGE APOPTOSIS; IL-1-BETA RELEASE; CELL-DEATH;
D O I
10.1038/s41573-021-00154-z
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Gasdermins were recently identified as the mediators of pyroptosis - inflammatory cell death triggered by cytosolic sensing of invasive infection and danger signals. Upon activation, gasdermins form cell membrane pores, which release pro-inflammatory cytokines and alarmins and damage the integrity of the cell membrane. Roles for gasdermins in autoimmune and inflammatory diseases, infectious diseases, deafness and cancer are emerging, revealing potential novel therapeutic avenues. Here, we review current knowledge of the family of gasdermins, focusing on their mechanisms of action and roles in normal physiology and disease. Efforts to develop drugs to modulate gasdermin activity to reduce inflammation or activate more potent immune responses are highlighted. Gasdermins (GSDMs) are a recently characterized protein family that mediate a programmed inflammatory cell death termed pyroptosis. Here, Lieberman and colleagues review current understanding of the expression, activation and regulation of GSDMs, highlighting their roles in cell death, cytokine secretion and inflammation. Emerging opportunities to develop GSDM-targeted drugs and the associated challenges are highlighted.
引用
收藏
页码:384 / 405
页数:22
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