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Inhibition of IRE1α RNase activity reduces NLRP3 inflammasome assembly and processing of pro-IL1β

The inflammasome is a multiprotein complex assembled in response to Pathogen Associated Molecular Patterns (PAMPs) and Danger Associated Molecular Patterns (DAMPs). Inflammasome activation occurs through a two-step mechanism, with the first signal facilitating priming of inflammasome components whil...

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Autores principales: Talty, Aaron, Deegan, Shane, Ljujic, Mila, Mnich, Katarzyna, Naicker, Serika D., Quandt, Dagmar, Zeng, Qingping, Patterson, John B., Gorman, Adrienne M., Griffin, Matthew D., Samali, Afshin, Logue, Susan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695440/
https://www.ncbi.nlm.nih.gov/pubmed/31417078
http://dx.doi.org/10.1038/s41419-019-1847-z
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author Talty, Aaron
Deegan, Shane
Ljujic, Mila
Mnich, Katarzyna
Naicker, Serika D.
Quandt, Dagmar
Zeng, Qingping
Patterson, John B.
Gorman, Adrienne M.
Griffin, Matthew D.
Samali, Afshin
Logue, Susan E.
author_facet Talty, Aaron
Deegan, Shane
Ljujic, Mila
Mnich, Katarzyna
Naicker, Serika D.
Quandt, Dagmar
Zeng, Qingping
Patterson, John B.
Gorman, Adrienne M.
Griffin, Matthew D.
Samali, Afshin
Logue, Susan E.
author_sort Talty, Aaron
collection PubMed
description The inflammasome is a multiprotein complex assembled in response to Pathogen Associated Molecular Patterns (PAMPs) and Danger Associated Molecular Patterns (DAMPs). Inflammasome activation occurs through a two-step mechanism, with the first signal facilitating priming of inflammasome components while the second signal triggers complex assembly. Once assembled, the inflammasome recruits and activates pro-caspase-1, which in turn processes pro-interleukin (IL)-18 and pro-IL-1β into their bio-active forms. Owing to its key role in the regulation of innate immune responses, the inflammasome has emerged as a therapeutic target for the treatment of inflammatory conditions. In this study we demonstrate that IRE1α, a key component of the Unfolded Protein Response, contributes to assembly of the NLRP3 inflammasome. Blockade of IRE1α RNase signaling lowered NLRP3 inflammasome assembly, caspase-1 activation and pro-IL-1β processing. These results underscore both the importance and potential therapeutic relevance of targeting IRE1α signaling in conditions of excessive inflammasome formation.
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spelling pubmed-66954402019-08-19 Inhibition of IRE1α RNase activity reduces NLRP3 inflammasome assembly and processing of pro-IL1β Talty, Aaron Deegan, Shane Ljujic, Mila Mnich, Katarzyna Naicker, Serika D. Quandt, Dagmar Zeng, Qingping Patterson, John B. Gorman, Adrienne M. Griffin, Matthew D. Samali, Afshin Logue, Susan E. Cell Death Dis Article The inflammasome is a multiprotein complex assembled in response to Pathogen Associated Molecular Patterns (PAMPs) and Danger Associated Molecular Patterns (DAMPs). Inflammasome activation occurs through a two-step mechanism, with the first signal facilitating priming of inflammasome components while the second signal triggers complex assembly. Once assembled, the inflammasome recruits and activates pro-caspase-1, which in turn processes pro-interleukin (IL)-18 and pro-IL-1β into their bio-active forms. Owing to its key role in the regulation of innate immune responses, the inflammasome has emerged as a therapeutic target for the treatment of inflammatory conditions. In this study we demonstrate that IRE1α, a key component of the Unfolded Protein Response, contributes to assembly of the NLRP3 inflammasome. Blockade of IRE1α RNase signaling lowered NLRP3 inflammasome assembly, caspase-1 activation and pro-IL-1β processing. These results underscore both the importance and potential therapeutic relevance of targeting IRE1α signaling in conditions of excessive inflammasome formation. Nature Publishing Group UK 2019-08-16 /pmc/articles/PMC6695440/ /pubmed/31417078 http://dx.doi.org/10.1038/s41419-019-1847-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Talty, Aaron
Deegan, Shane
Ljujic, Mila
Mnich, Katarzyna
Naicker, Serika D.
Quandt, Dagmar
Zeng, Qingping
Patterson, John B.
Gorman, Adrienne M.
Griffin, Matthew D.
Samali, Afshin
Logue, Susan E.
Inhibition of IRE1α RNase activity reduces NLRP3 inflammasome assembly and processing of pro-IL1β
title Inhibition of IRE1α RNase activity reduces NLRP3 inflammasome assembly and processing of pro-IL1β
title_full Inhibition of IRE1α RNase activity reduces NLRP3 inflammasome assembly and processing of pro-IL1β
title_fullStr Inhibition of IRE1α RNase activity reduces NLRP3 inflammasome assembly and processing of pro-IL1β
title_full_unstemmed Inhibition of IRE1α RNase activity reduces NLRP3 inflammasome assembly and processing of pro-IL1β
title_short Inhibition of IRE1α RNase activity reduces NLRP3 inflammasome assembly and processing of pro-IL1β
title_sort inhibition of ire1α rnase activity reduces nlrp3 inflammasome assembly and processing of pro-il1β
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695440/
https://www.ncbi.nlm.nih.gov/pubmed/31417078
http://dx.doi.org/10.1038/s41419-019-1847-z
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