炎症体
调节器
上睑下垂
半胱氨酸蛋白酶1
细胞生物学
炎症
化学
胞浆
谷胱甘肽
生物
酶
生物化学
基因
免疫学
作者
Mark Hughes,Alexander Hooftman,Stefano Angiari,Padmaja Tummala,Zbigniew Zasłona,Marah C. Runtsch,Anne F. McGettrick,Caroline E. Sutton,Ciana Diskin,Melissa Rooke,Shuhei Takahashi,Srinivasan Sundararaj,Marco G. Casarotto,Jane E. Dahlstrom,Eva M. Pålsson‐McDermott,Sinéad C. Corr,Kingston H. G. Mills,Roger J. S. Preston,Nouri Neamati,Yiyue Xie,Jonathan B. Baell,Philip G. Board,Luke O'neill
出处
期刊:Cell Reports
[Elsevier]
日期:2019-10-01
卷期号:29 (1): 151-161.e5
被引量:70
标识
DOI:10.1016/j.celrep.2019.08.072
摘要
The NLRP3 inflammasome is a cytosolic complex sensing phagocytosed material and various damage-associated molecular patterns, triggering production of the pro-inflammatory cytokines interleukin-1 beta (IL)-1β and IL-18 and promoting pyroptosis. Here, we characterize glutathione transferase omega 1-1 (GSTO1-1), a constitutive deglutathionylating enzyme, as a regulator of the NLRP3 inflammasome. Using a small molecule inhibitor of GSTO1-1 termed C1-27, endogenous GSTO1-1 knockdown, and GSTO1-1-/- mice, we report that GSTO1-1 is involved in NLRP3 inflammasome activation. Mechanistically, GSTO1-1 deglutathionylates cysteine 253 in NIMA related kinase 7 (NEK7) to promote NLRP3 activation. We therefore identify GSTO1-1 as an NLRP3 inflammasome regulator, which has potential as a drug target to limit NLRP3-mediated inflammation.
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