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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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.
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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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