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Cytoplasmic innate immune sensing by the caspase-4 non-canonical inflammasome promotes cellular senescence
Cytoplasmic recognition of microbial lipopolysaccharides (LPS) in human cells is elicited by the caspase-4 and caspase-5 noncanonical inflammasomes, which induce a form of inflammatory cell death termed pyroptosis. Here we show that LPS-mediated activation of caspase-4 also induces a stress response...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177556/ https://www.ncbi.nlm.nih.gov/pubmed/34916628 http://dx.doi.org/10.1038/s41418-021-00917-6 |
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author | Fernández-Duran, Irene Quintanilla, Andrea Tarrats, Núria Birch, Jodie Hari, Priya Millar, Fraser R. Lagnado, Anthony B. Smer-Barreto, Vanessa Muir, Morwenna Brunton, Valerie G. Passos, João F. Acosta, Juan Carlos |
author_facet | Fernández-Duran, Irene Quintanilla, Andrea Tarrats, Núria Birch, Jodie Hari, Priya Millar, Fraser R. Lagnado, Anthony B. Smer-Barreto, Vanessa Muir, Morwenna Brunton, Valerie G. Passos, João F. Acosta, Juan Carlos |
author_sort | Fernández-Duran, Irene |
collection | PubMed |
description | Cytoplasmic recognition of microbial lipopolysaccharides (LPS) in human cells is elicited by the caspase-4 and caspase-5 noncanonical inflammasomes, which induce a form of inflammatory cell death termed pyroptosis. Here we show that LPS-mediated activation of caspase-4 also induces a stress response promoting cellular senescence, which is dependent on the caspase-4 substrate gasdermin-D and the tumor suppressor p53. Furthermore, we found that the caspase-4 noncanonical inflammasome is induced and assembled in response to oncogenic RAS signaling during oncogene-induced senescence (OIS). Moreover, targeting caspase-4 expression in OIS showed its critical role in the senescence-associated secretory phenotype and the cell cycle arrest induced in cellular senescence. Finally, we observed that caspase-4 induction occurs in vivo in mouse models of tumor suppression and ageing. Altogether, we are showing that cellular senescence is induced by cytoplasmic LPS recognition by the noncanonical inflammasome and that this pathway is conserved in the cellular response to oncogenic stress. |
format | Online Article Text |
id | pubmed-9177556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91775562022-06-10 Cytoplasmic innate immune sensing by the caspase-4 non-canonical inflammasome promotes cellular senescence Fernández-Duran, Irene Quintanilla, Andrea Tarrats, Núria Birch, Jodie Hari, Priya Millar, Fraser R. Lagnado, Anthony B. Smer-Barreto, Vanessa Muir, Morwenna Brunton, Valerie G. Passos, João F. Acosta, Juan Carlos Cell Death Differ Article Cytoplasmic recognition of microbial lipopolysaccharides (LPS) in human cells is elicited by the caspase-4 and caspase-5 noncanonical inflammasomes, which induce a form of inflammatory cell death termed pyroptosis. Here we show that LPS-mediated activation of caspase-4 also induces a stress response promoting cellular senescence, which is dependent on the caspase-4 substrate gasdermin-D and the tumor suppressor p53. Furthermore, we found that the caspase-4 noncanonical inflammasome is induced and assembled in response to oncogenic RAS signaling during oncogene-induced senescence (OIS). Moreover, targeting caspase-4 expression in OIS showed its critical role in the senescence-associated secretory phenotype and the cell cycle arrest induced in cellular senescence. Finally, we observed that caspase-4 induction occurs in vivo in mouse models of tumor suppression and ageing. Altogether, we are showing that cellular senescence is induced by cytoplasmic LPS recognition by the noncanonical inflammasome and that this pathway is conserved in the cellular response to oncogenic stress. Nature Publishing Group UK 2021-12-16 2022-06 /pmc/articles/PMC9177556/ /pubmed/34916628 http://dx.doi.org/10.1038/s41418-021-00917-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Fernández-Duran, Irene Quintanilla, Andrea Tarrats, Núria Birch, Jodie Hari, Priya Millar, Fraser R. Lagnado, Anthony B. Smer-Barreto, Vanessa Muir, Morwenna Brunton, Valerie G. Passos, João F. Acosta, Juan Carlos Cytoplasmic innate immune sensing by the caspase-4 non-canonical inflammasome promotes cellular senescence |
title | Cytoplasmic innate immune sensing by the caspase-4 non-canonical inflammasome promotes cellular senescence |
title_full | Cytoplasmic innate immune sensing by the caspase-4 non-canonical inflammasome promotes cellular senescence |
title_fullStr | Cytoplasmic innate immune sensing by the caspase-4 non-canonical inflammasome promotes cellular senescence |
title_full_unstemmed | Cytoplasmic innate immune sensing by the caspase-4 non-canonical inflammasome promotes cellular senescence |
title_short | Cytoplasmic innate immune sensing by the caspase-4 non-canonical inflammasome promotes cellular senescence |
title_sort | cytoplasmic innate immune sensing by the caspase-4 non-canonical inflammasome promotes cellular senescence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177556/ https://www.ncbi.nlm.nih.gov/pubmed/34916628 http://dx.doi.org/10.1038/s41418-021-00917-6 |
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