Pathogen blockade of TAK1 triggers caspase-8-dependent cleavage of gasdermin D and cell death

被引:715
|
作者
Orning, Pontus [1 ,2 ]
Weng, Dan [1 ,3 ]
Starheim, Kristian [1 ,2 ]
Ratner, Dmitry [1 ]
Best, Zachary [1 ]
Lee, Bettina [4 ]
Brooks, Alexandria [1 ]
Xia, Shiyu [5 ,6 ]
Wu, Hao [5 ,6 ]
Kelliher, Michelle A. [7 ]
Berger, Scott B. [8 ]
Gough, Peter J. [8 ]
Bertin, John [8 ]
Proulx, Megan M. [9 ]
Goguen, Jon D. [9 ]
Kayagaki, Nobuhiko [4 ]
Fitzgerald, Katherine A. [2 ]
Lien, Egil [1 ,2 ]
机构
[1] Univ Massachusetts, Div Infect Dis & Immunol, Dept Med, Program Innate Immun,Med Sch, Worcester, MA 01605 USA
[2] Norwegian Univ Sci & Technol, Dept Clin & Mol Med, Ctr Mol Inflammat Res, N-7491 Trondheim, Norway
[3] Nanjing Univ Sci & Technol, Ctr Mol Metab, Nanjing 210094, Jiangsu, Peoples R China
[4] Genentech Inc, Dept Physiol Chem, San Francisco, CA 94080 USA
[5] Harvard Med Sch, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[6] Boston Childrens Hosp, Program Cellular & Mol Med, Boston, MA 02115 USA
[7] Univ Massachusetts, Dept Canc Biol, Med Sch, Worcester, MA 01605 USA
[8] GlaxoSmithKline, Pattern Recognit Receptor Discovery Performance U, Immunoinflammat Therapeut Area, Collegeville, PA 19426 USA
[9] Univ Massachusetts, Dept Microbiol & Physiol, Med Sch, Worcester, MA 01655 USA
基金
美国国家卫生研究院;
关键词
NF-KAPPA-B; YERSINIA-PESTIS; ACTIVATION; CASPASE-1; PYROPTOSIS; NECROSIS; GSDMD; TRIF; PHOSPHORYLATION; COLONIZATION;
D O I
10.1126/science.aau2818
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Limited proteolysis of gasdermin D (GSDMD) generates an N-terminal pore-forming fragment that controls pyroptosis in macrophages. GSDMD is processed via inflammasome-activated caspase-1 or -11. It is currently unknown whether macrophage GSDMD can be processed by other mechanisms. Here, we describe an additional pathway controlling GSDMD processing. The inhibition of TAK1 or I kappa B kinase (IKK) by the Yersinia effector protein YopJ elicits RIPK1- and caspase-8-dependent cleavage of GSDMD, which subsequently results in cell death. GSDMD processing also contributes to the NLRP3 inflammasome-dependent release of interleukin-1 beta (IL-1 beta). Thus, caspase-8 acts as a regulator of GSDMD-driven cell death. Furthermore, this study establishes the importance of TAK1 and IKK activity in the control of GSDMD cleavage and cytotoxicity.
引用
收藏
页码:1064 / +
页数:32
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