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Resveratrol suppresses NTHi-induced inflammation via up-regulation of the negative regulator MyD88 short
Upper respiratory tract inflammatory diseases such as asthma and chronic obstructive pulmonary diseases (COPD) affect more than one-half billion people globally and are characterized by chronic inflammation that is often exacerbated by respiratory pathogens such as nontypeable Haemophilus influenzae...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039644/ https://www.ncbi.nlm.nih.gov/pubmed/27677845 http://dx.doi.org/10.1038/srep34445 |
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author | Andrews, Carla S. Matsuyama, Shingo Lee, Byung-Cheol Li, Jian-Dong |
author_facet | Andrews, Carla S. Matsuyama, Shingo Lee, Byung-Cheol Li, Jian-Dong |
author_sort | Andrews, Carla S. |
collection | PubMed |
description | Upper respiratory tract inflammatory diseases such as asthma and chronic obstructive pulmonary diseases (COPD) affect more than one-half billion people globally and are characterized by chronic inflammation that is often exacerbated by respiratory pathogens such as nontypeable Haemophilus influenzae (NTHi). The increasing numbers of antibiotic-resistant bacterial strains and the limited success of currently available pharmaceuticals used to manage the symptoms of these diseases present an urgent need for the development of novel anti-inflammatory therapeutic agents. Resveratrol has long been thought as an interesting therapeutic agent for various diseases including inflammatory diseases. However, the molecular mechanisms underlying its anti-inflammatory properties remain largely unknown. Here we show for the first time that resveratrol decreases expression of pro-inflammatory mediators in airway epithelial cells and in the lung of mice by enhancing NTHi-induced MyD88 short, a negative regulator of inflammation, via inhibition of ERK1/2 activation. Furthermore, resveratrol inhibits NTHi-induced ERK1/2 phosphorylation by increasing MKP-1 expression via a cAMP-PKA-dependent signaling pathway. Finally, we show that resveratrol has anti-inflammatory effects post NTHi infection, thereby demonstrating its therapeutic potential. Together these data reveal a novel mechanism by which resveratrol alleviates NTHi-induced inflammation in airway disease by up-regulating the negative regulator of inflammation MyD88s. |
format | Online Article Text |
id | pubmed-5039644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50396442016-09-30 Resveratrol suppresses NTHi-induced inflammation via up-regulation of the negative regulator MyD88 short Andrews, Carla S. Matsuyama, Shingo Lee, Byung-Cheol Li, Jian-Dong Sci Rep Article Upper respiratory tract inflammatory diseases such as asthma and chronic obstructive pulmonary diseases (COPD) affect more than one-half billion people globally and are characterized by chronic inflammation that is often exacerbated by respiratory pathogens such as nontypeable Haemophilus influenzae (NTHi). The increasing numbers of antibiotic-resistant bacterial strains and the limited success of currently available pharmaceuticals used to manage the symptoms of these diseases present an urgent need for the development of novel anti-inflammatory therapeutic agents. Resveratrol has long been thought as an interesting therapeutic agent for various diseases including inflammatory diseases. However, the molecular mechanisms underlying its anti-inflammatory properties remain largely unknown. Here we show for the first time that resveratrol decreases expression of pro-inflammatory mediators in airway epithelial cells and in the lung of mice by enhancing NTHi-induced MyD88 short, a negative regulator of inflammation, via inhibition of ERK1/2 activation. Furthermore, resveratrol inhibits NTHi-induced ERK1/2 phosphorylation by increasing MKP-1 expression via a cAMP-PKA-dependent signaling pathway. Finally, we show that resveratrol has anti-inflammatory effects post NTHi infection, thereby demonstrating its therapeutic potential. Together these data reveal a novel mechanism by which resveratrol alleviates NTHi-induced inflammation in airway disease by up-regulating the negative regulator of inflammation MyD88s. Nature Publishing Group 2016-09-28 /pmc/articles/PMC5039644/ /pubmed/27677845 http://dx.doi.org/10.1038/srep34445 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Andrews, Carla S. Matsuyama, Shingo Lee, Byung-Cheol Li, Jian-Dong Resveratrol suppresses NTHi-induced inflammation via up-regulation of the negative regulator MyD88 short |
title | Resveratrol suppresses NTHi-induced inflammation via up-regulation of the negative regulator MyD88 short |
title_full | Resveratrol suppresses NTHi-induced inflammation via up-regulation of the negative regulator MyD88 short |
title_fullStr | Resveratrol suppresses NTHi-induced inflammation via up-regulation of the negative regulator MyD88 short |
title_full_unstemmed | Resveratrol suppresses NTHi-induced inflammation via up-regulation of the negative regulator MyD88 short |
title_short | Resveratrol suppresses NTHi-induced inflammation via up-regulation of the negative regulator MyD88 short |
title_sort | resveratrol suppresses nthi-induced inflammation via up-regulation of the negative regulator myd88 short |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039644/ https://www.ncbi.nlm.nih.gov/pubmed/27677845 http://dx.doi.org/10.1038/srep34445 |
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