Early endosome autoantigen 1 regulates IL-1β release upon caspase-1 activation independently of gasdermin D membrane permeabilization

被引:22
作者
Baroja-Mazo, Alberto [1 ]
Compan, Vincent [2 ,3 ]
Martin-Sanchez, Fatima [1 ]
Tapia-Abellan, Ana [1 ]
Couillin, Isabelle [4 ]
Pelegrin, Pablo [1 ]
机构
[1] Clin Univ Hosp Virgen de la Arrixaca, Inflammat & Expt Surg Unit, Biomed Res Inst Murcia IMIB Arrixaca, Murcia 30120, Spain
[2] Inst Funct Genom, Labex ICST, F-34094 Montpellier 5, France
[3] Univ Montpellier 141, CNRS UMR5203, INSERM U661, F-34094 Montpellier 5, France
[4] Univ Orleans, UMR7355, Mol & Expt Immunol & Neurogenet, NEM,CNRS, F-45071 Orleans, France
关键词
NLRP3; INFLAMMASOME; ACTIVE CASPASE-1; PLASMA-MEMBRANE; SECRETION; EEA1; MECHANISM; PROTEIN; INTERLEUKIN-1-BETA; PYROPTOSIS; AUTOANTIBODIES;
D O I
10.1038/s41598-019-42298-4
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
Unconventional protein secretion represents an important process of the inflammatory response. The release of the pro-inflammatory cytokine interleukin (IL)-1 beta which burst during pyroptosis as a consequence of gasdermin D plasma membrane pore formation, can also occur through other unconventional secretion pathways dependent on caspase-1 activation. However, how caspase-1 mediates cytokine release independently of gasdermin D remains poorly understood. Here we show that following caspase-1 activation by different inflammasomes, caspase-1 cleaves early endosome autoantigen 1 (EEA1) protein at Asp(127/132). Caspase-1 activation also results in the release of the endosomal EEA1 protein in a gasdermin D-independent manner. EEA1 knock-down results in adecreased release of caspase-1 and IL-1 beta, but the pyroptotic release of other inflammasome components and lactate dehydrogenase was not affected. This study shows how caspase-1 control the release of EEA1 and IL-1 beta in a pyroptotic-independent manner.
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页数:10
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