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Short-chain fatty acids bind to apoptosis-associated speck-like protein to activate inflammasome complex to prevent Salmonella infection

Short-chain fatty acids (SCFAs) produced by gastrointestinal microbiota regulate immune responses, but host molecular mechanisms remain unknown. Unbiased screening using SCFA-conjugated affinity nanobeads identified apoptosis-associated speck-like protein (ASC), an adaptor protein of inflammasome co...

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Autores principales: Tsugawa, Hitoshi, Kabe, Yasuaki, Kanai, Ayaka, Sugiura, Yuki, Hida, Shigeaki, Taniguchi, Shun’ichiro, Takahashi, Toshio, Matsui, Hidenori, Yasukawa, Zenta, Itou, Hiroyuki, Takubo, Keiyo, Suzuki, Hidekazu, Honda, Kenya, Handa, Hiroshi, Suematsu, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524008/
https://www.ncbi.nlm.nih.gov/pubmed/32991574
http://dx.doi.org/10.1371/journal.pbio.3000813
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author Tsugawa, Hitoshi
Kabe, Yasuaki
Kanai, Ayaka
Sugiura, Yuki
Hida, Shigeaki
Taniguchi, Shun’ichiro
Takahashi, Toshio
Matsui, Hidenori
Yasukawa, Zenta
Itou, Hiroyuki
Takubo, Keiyo
Suzuki, Hidekazu
Honda, Kenya
Handa, Hiroshi
Suematsu, Makoto
author_facet Tsugawa, Hitoshi
Kabe, Yasuaki
Kanai, Ayaka
Sugiura, Yuki
Hida, Shigeaki
Taniguchi, Shun’ichiro
Takahashi, Toshio
Matsui, Hidenori
Yasukawa, Zenta
Itou, Hiroyuki
Takubo, Keiyo
Suzuki, Hidekazu
Honda, Kenya
Handa, Hiroshi
Suematsu, Makoto
author_sort Tsugawa, Hitoshi
collection PubMed
description Short-chain fatty acids (SCFAs) produced by gastrointestinal microbiota regulate immune responses, but host molecular mechanisms remain unknown. Unbiased screening using SCFA-conjugated affinity nanobeads identified apoptosis-associated speck-like protein (ASC), an adaptor protein of inflammasome complex, as a noncanonical SCFA receptor besides GPRs. SCFAs promoted inflammasome activation in macrophages by binding to its ASC PYRIN domain. Activated inflammasome suppressed survival of Salmonella enterica serovar Typhimurium (S. Typhimurium) in macrophages by pyroptosis and facilitated neutrophil recruitment to promote bacterial elimination and thus inhibit systemic dissemination in the host. Administration of SCFAs or dietary fibers, which are fermented to SCFAs by gut bacteria, significantly prolonged the survival of S. Typhimurium–infected mice through ASC-mediated inflammasome activation. SCFAs penetrated into the inflammatory region of the infected gut mucosa to protect against infection. This study provided evidence that SCFAs suppress Salmonella infection via inflammasome activation, shedding new light on the therapeutic activity of dietary fiber.
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spelling pubmed-75240082020-10-06 Short-chain fatty acids bind to apoptosis-associated speck-like protein to activate inflammasome complex to prevent Salmonella infection Tsugawa, Hitoshi Kabe, Yasuaki Kanai, Ayaka Sugiura, Yuki Hida, Shigeaki Taniguchi, Shun’ichiro Takahashi, Toshio Matsui, Hidenori Yasukawa, Zenta Itou, Hiroyuki Takubo, Keiyo Suzuki, Hidekazu Honda, Kenya Handa, Hiroshi Suematsu, Makoto PLoS Biol Research Article Short-chain fatty acids (SCFAs) produced by gastrointestinal microbiota regulate immune responses, but host molecular mechanisms remain unknown. Unbiased screening using SCFA-conjugated affinity nanobeads identified apoptosis-associated speck-like protein (ASC), an adaptor protein of inflammasome complex, as a noncanonical SCFA receptor besides GPRs. SCFAs promoted inflammasome activation in macrophages by binding to its ASC PYRIN domain. Activated inflammasome suppressed survival of Salmonella enterica serovar Typhimurium (S. Typhimurium) in macrophages by pyroptosis and facilitated neutrophil recruitment to promote bacterial elimination and thus inhibit systemic dissemination in the host. Administration of SCFAs or dietary fibers, which are fermented to SCFAs by gut bacteria, significantly prolonged the survival of S. Typhimurium–infected mice through ASC-mediated inflammasome activation. SCFAs penetrated into the inflammatory region of the infected gut mucosa to protect against infection. This study provided evidence that SCFAs suppress Salmonella infection via inflammasome activation, shedding new light on the therapeutic activity of dietary fiber. Public Library of Science 2020-09-29 /pmc/articles/PMC7524008/ /pubmed/32991574 http://dx.doi.org/10.1371/journal.pbio.3000813 Text en © 2020 Tsugawa et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Tsugawa, Hitoshi
Kabe, Yasuaki
Kanai, Ayaka
Sugiura, Yuki
Hida, Shigeaki
Taniguchi, Shun’ichiro
Takahashi, Toshio
Matsui, Hidenori
Yasukawa, Zenta
Itou, Hiroyuki
Takubo, Keiyo
Suzuki, Hidekazu
Honda, Kenya
Handa, Hiroshi
Suematsu, Makoto
Short-chain fatty acids bind to apoptosis-associated speck-like protein to activate inflammasome complex to prevent Salmonella infection
title Short-chain fatty acids bind to apoptosis-associated speck-like protein to activate inflammasome complex to prevent Salmonella infection
title_full Short-chain fatty acids bind to apoptosis-associated speck-like protein to activate inflammasome complex to prevent Salmonella infection
title_fullStr Short-chain fatty acids bind to apoptosis-associated speck-like protein to activate inflammasome complex to prevent Salmonella infection
title_full_unstemmed Short-chain fatty acids bind to apoptosis-associated speck-like protein to activate inflammasome complex to prevent Salmonella infection
title_short Short-chain fatty acids bind to apoptosis-associated speck-like protein to activate inflammasome complex to prevent Salmonella infection
title_sort short-chain fatty acids bind to apoptosis-associated speck-like protein to activate inflammasome complex to prevent salmonella infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524008/
https://www.ncbi.nlm.nih.gov/pubmed/32991574
http://dx.doi.org/10.1371/journal.pbio.3000813
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