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ATP release and purinergic signaling: a common pathway for particle-mediated inflammasome activation
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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3481132/ https://www.ncbi.nlm.nih.gov/pubmed/23059822 http://dx.doi.org/10.1038/cddis.2012.144 |
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author | Riteau, N Baron, L Villeret, B Guillou, N Savigny, F Ryffel, B Rassendren, F Le Bert, M Gombault, A Couillin, I |
author_facet | Riteau, N Baron, L Villeret, B Guillou, N Savigny, F Ryffel, B Rassendren, F Le Bert, M Gombault, A Couillin, I |
author_sort | Riteau, N |
collection | PubMed |
description | 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-1β (IL-1β) 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-1β 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. |
format | Online Article Text |
id | pubmed-3481132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-34811322012-10-26 ATP release and purinergic signaling: a common pathway for particle-mediated inflammasome activation Riteau, N Baron, L Villeret, B Guillou, N Savigny, F Ryffel, B Rassendren, F Le Bert, M Gombault, A Couillin, I Cell Death Dis Original Article 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-1β (IL-1β) 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-1β 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. Nature Publishing Group 2012-10 2012-10-11 /pmc/articles/PMC3481132/ /pubmed/23059822 http://dx.doi.org/10.1038/cddis.2012.144 Text en Copyright © 2012 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Riteau, N Baron, L Villeret, B Guillou, N Savigny, F Ryffel, B Rassendren, F Le Bert, M Gombault, A Couillin, I ATP release and purinergic signaling: a common pathway for particle-mediated inflammasome activation |
title | ATP release and purinergic signaling: a common pathway for particle-mediated inflammasome activation |
title_full | ATP release and purinergic signaling: a common pathway for particle-mediated inflammasome activation |
title_fullStr | ATP release and purinergic signaling: a common pathway for particle-mediated inflammasome activation |
title_full_unstemmed | ATP release and purinergic signaling: a common pathway for particle-mediated inflammasome activation |
title_short | ATP release and purinergic signaling: a common pathway for particle-mediated inflammasome activation |
title_sort | atp release and purinergic signaling: a common pathway for particle-mediated inflammasome activation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3481132/ https://www.ncbi.nlm.nih.gov/pubmed/23059822 http://dx.doi.org/10.1038/cddis.2012.144 |
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