共 22 条
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
来源:
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.
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页码:1064 / +
页数:32
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