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Bacterial recognition pathways that lead to inflammasome activation

Inflammasomes are multi-protein signaling platforms that upon activation trigger the maturation of the pro-inflammatory cytokines, interleukin-1β (IL-1β) and IL-18, and cell death. Inflammasome sensors detect microbial and host-derived molecules. Here, we review the mechanisms of inflammasome activa...

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Detalles Bibliográficos
Autores principales: Storek, Kelly M, Monack, Denise M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437016/
https://www.ncbi.nlm.nih.gov/pubmed/25879288
http://dx.doi.org/10.1111/imr.12289
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author Storek, Kelly M
Monack, Denise M
author_facet Storek, Kelly M
Monack, Denise M
author_sort Storek, Kelly M
collection PubMed
description Inflammasomes are multi-protein signaling platforms that upon activation trigger the maturation of the pro-inflammatory cytokines, interleukin-1β (IL-1β) and IL-18, and cell death. Inflammasome sensors detect microbial and host-derived molecules. Here, we review the mechanisms of inflammasome activation triggered by bacterial infection, primarily focusing on two model intracellular bacterial pathogens, Francisella novicida and Salmonella typhimurium. We discuss the complex relationship between bacterial recognition through direct and indirect detection by inflammasome sensors. We highlight regulation mechanisms that potentiate or limit inflammasome activation. We discuss the importance of caspase-1 and caspase-11 in host defense, and we examine the downstream consequences of inflammasome activation within the context of bacterial infections.
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spelling pubmed-44370162015-05-28 Bacterial recognition pathways that lead to inflammasome activation Storek, Kelly M Monack, Denise M Immunol Rev Invited Reviews Inflammasomes are multi-protein signaling platforms that upon activation trigger the maturation of the pro-inflammatory cytokines, interleukin-1β (IL-1β) and IL-18, and cell death. Inflammasome sensors detect microbial and host-derived molecules. Here, we review the mechanisms of inflammasome activation triggered by bacterial infection, primarily focusing on two model intracellular bacterial pathogens, Francisella novicida and Salmonella typhimurium. We discuss the complex relationship between bacterial recognition through direct and indirect detection by inflammasome sensors. We highlight regulation mechanisms that potentiate or limit inflammasome activation. We discuss the importance of caspase-1 and caspase-11 in host defense, and we examine the downstream consequences of inflammasome activation within the context of bacterial infections. Blackwell Publishing Ltd 2015-05 2015-04-16 /pmc/articles/PMC4437016/ /pubmed/25879288 http://dx.doi.org/10.1111/imr.12289 Text en © 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Invited Reviews
Storek, Kelly M
Monack, Denise M
Bacterial recognition pathways that lead to inflammasome activation
title Bacterial recognition pathways that lead to inflammasome activation
title_full Bacterial recognition pathways that lead to inflammasome activation
title_fullStr Bacterial recognition pathways that lead to inflammasome activation
title_full_unstemmed Bacterial recognition pathways that lead to inflammasome activation
title_short Bacterial recognition pathways that lead to inflammasome activation
title_sort bacterial recognition pathways that lead to inflammasome activation
topic Invited Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437016/
https://www.ncbi.nlm.nih.gov/pubmed/25879288
http://dx.doi.org/10.1111/imr.12289
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