Cargando…
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...
Autores principales: | , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783444040463679488 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6695440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT taltyaaron inhibitionofire1arnaseactivityreducesnlrp3inflammasomeassemblyandprocessingofproil1b AT deeganshane inhibitionofire1arnaseactivityreducesnlrp3inflammasomeassemblyandprocessingofproil1b AT ljujicmila inhibitionofire1arnaseactivityreducesnlrp3inflammasomeassemblyandprocessingofproil1b AT mnichkatarzyna inhibitionofire1arnaseactivityreducesnlrp3inflammasomeassemblyandprocessingofproil1b AT naickerserikad inhibitionofire1arnaseactivityreducesnlrp3inflammasomeassemblyandprocessingofproil1b AT quandtdagmar inhibitionofire1arnaseactivityreducesnlrp3inflammasomeassemblyandprocessingofproil1b AT zengqingping inhibitionofire1arnaseactivityreducesnlrp3inflammasomeassemblyandprocessingofproil1b AT pattersonjohnb inhibitionofire1arnaseactivityreducesnlrp3inflammasomeassemblyandprocessingofproil1b AT gormanadriennem inhibitionofire1arnaseactivityreducesnlrp3inflammasomeassemblyandprocessingofproil1b AT griffinmatthewd inhibitionofire1arnaseactivityreducesnlrp3inflammasomeassemblyandprocessingofproil1b AT samaliafshin inhibitionofire1arnaseactivityreducesnlrp3inflammasomeassemblyandprocessingofproil1b AT loguesusane inhibitionofire1arnaseactivityreducesnlrp3inflammasomeassemblyandprocessingofproil1b |