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Influenza virus activates inflammasomes through intracellular M2 channel

Influenza virus, a negative stranded RNA virus causing severe illness in humans and animals, stimulates the inflammasome through the NOD-like receptor (NLR), NLRP3. However, the mechanism by which influenza virus activates the NLRP3 inflammasome is unknown. Here, we show that the influenza virus M2...

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Autores principales: Ichinohe, Takeshi, Pang, Iris Kok-shuen, Iwasaki, Akiko
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2857582/
https://www.ncbi.nlm.nih.gov/pubmed/20383149
http://dx.doi.org/10.1038/ni.1861
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author Ichinohe, Takeshi
Pang, Iris Kok-shuen
Iwasaki, Akiko
author_facet Ichinohe, Takeshi
Pang, Iris Kok-shuen
Iwasaki, Akiko
author_sort Ichinohe, Takeshi
collection PubMed
description Influenza virus, a negative stranded RNA virus causing severe illness in humans and animals, stimulates the inflammasome through the NOD-like receptor (NLR), NLRP3. However, the mechanism by which influenza virus activates the NLRP3 inflammasome is unknown. Here, we show that the influenza virus M2 protein, a proton-selective ion channel important in viral pathogenesis, stimulates the NLRP3 inflammasome pathway. M2 channel activity was required for influenza activation of inflammasomes, and was sufficient to activate inflammasomes in primed macrophages and dendritic cells. M2-induced inflammasome activation required its localization to Golgi and was dependent on pH gradient. Our results reveal a mechanism by which influenza virus infection activates inflammasomes, and identifies the sensing of disturbances in intracellular ionic concentrations as a novel pathogen recognition pathway.
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spelling pubmed-28575822010-11-01 Influenza virus activates inflammasomes through intracellular M2 channel Ichinohe, Takeshi Pang, Iris Kok-shuen Iwasaki, Akiko Nat Immunol Article Influenza virus, a negative stranded RNA virus causing severe illness in humans and animals, stimulates the inflammasome through the NOD-like receptor (NLR), NLRP3. However, the mechanism by which influenza virus activates the NLRP3 inflammasome is unknown. Here, we show that the influenza virus M2 protein, a proton-selective ion channel important in viral pathogenesis, stimulates the NLRP3 inflammasome pathway. M2 channel activity was required for influenza activation of inflammasomes, and was sufficient to activate inflammasomes in primed macrophages and dendritic cells. M2-induced inflammasome activation required its localization to Golgi and was dependent on pH gradient. Our results reveal a mechanism by which influenza virus infection activates inflammasomes, and identifies the sensing of disturbances in intracellular ionic concentrations as a novel pathogen recognition pathway. 2010-04-11 2010-05 /pmc/articles/PMC2857582/ /pubmed/20383149 http://dx.doi.org/10.1038/ni.1861 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Ichinohe, Takeshi
Pang, Iris Kok-shuen
Iwasaki, Akiko
Influenza virus activates inflammasomes through intracellular M2 channel
title Influenza virus activates inflammasomes through intracellular M2 channel
title_full Influenza virus activates inflammasomes through intracellular M2 channel
title_fullStr Influenza virus activates inflammasomes through intracellular M2 channel
title_full_unstemmed Influenza virus activates inflammasomes through intracellular M2 channel
title_short Influenza virus activates inflammasomes through intracellular M2 channel
title_sort influenza virus activates inflammasomes through intracellular m2 channel
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2857582/
https://www.ncbi.nlm.nih.gov/pubmed/20383149
http://dx.doi.org/10.1038/ni.1861
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