ATP release and purinergic signaling: a common pathway for particle-mediated inflammasome activation

被引:238
作者
Riteau, N. [1 ]
Baron, L. [1 ]
Villeret, B. [1 ]
Guillou, N. [1 ]
Savigny, F. [1 ]
Ryffel, B. [1 ]
Rassendren, F. [2 ,3 ]
Le Bert, M. [1 ]
Gombault, A. [1 ]
Couillin, I. [1 ]
机构
[1] Univ Orleans, INEM, UMR7355, Transgenose Inst,CNRS, F-45071 Orleans, France
[2] Univ Montpellier I, IGF, CNRS UMR 5203, INSERM U661, Montpellier, France
[3] Univ Montpellier 2, IGF, CNRS UMR 5203, INSERM U661, Montpellier, France
关键词
ATP; danger signal; inflammasome; P2R; NLR; NALP3; INFLAMMASOME; P2X(7) RECEPTOR; DANGER SIGNAL; INTERLEUKIN-1-BETA RELEASE; DIFFERENTIAL REQUIREMENT; CASPASE-1; ACTIVATION; NLRP3; AMYLOID-BETA; URIC-ACID; PANNEXIN-1;
D O I
10.1038/cddis.2012.144
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Deposition of uric acid crystals in joints causes the acute and chronic inflammatory disease known as gout and prolonged airway exposure to silica crystals leads to the development of silicosis, an irreversible fibrotic pulmonary disease. Aluminum salt (Alum) crystals are frequently used as vaccine adjuvant. The mechanisms by which crystals activate innate immunity through the Nlrp3 inflammasome are not well understood. Here, we show that uric acid, silica and Alum crystals trigger the extracellular delivery of endogenous ATP, which just precedes the secretion of mature interleukin-1b (IL-1b) by macrophages, both events depending on purinergic receptors and connexin/pannexin channels. Interestingly, not only ATP but also ADP and UTP are involved in IL-1b production upon these Nlrp3 inflammasome activators through multiple purinergic receptor signaling. These findings support a pivotal role for nucleotides as danger signals and provide a new molecular mechanism to explain how chemically and structurally diverse stimuli can activate the Nlrp3 inflammasome. Cell Death and Disease (2012) 3, e403; doi:10.1038/cddis.2012.144; published online 11 October 2012
引用
收藏
页码:e403 / e403
页数:10
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