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DUOX-Mediated Signaling Is Not Required for LPS-Induced Neutrophilic Response in the Airways

Oxidant production from DUOX1 has been proposed to lead to neutrophil recruitment into the airways when lung homeostasis is compromised. The objective of this study was to determine whether DUOX-derived hydrogen peroxide is required for LPS-induced neutrophil recruitment, using a functional DUOX kno...

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Detalles Bibliográficos
Autores principales: Chang, Sandra, Linderholm, Angela, Harper, Richart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493023/
https://www.ncbi.nlm.nih.gov/pubmed/26148206
http://dx.doi.org/10.1371/journal.pone.0131810
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author Chang, Sandra
Linderholm, Angela
Harper, Richart
author_facet Chang, Sandra
Linderholm, Angela
Harper, Richart
author_sort Chang, Sandra
collection PubMed
description Oxidant production from DUOX1 has been proposed to lead to neutrophil recruitment into the airways when lung homeostasis is compromised. The objective of this study was to determine whether DUOX-derived hydrogen peroxide is required for LPS-induced neutrophil recruitment, using a functional DUOX knock out mouse model. We found that LPS induced profound neutrophilic lung inflammation in both Duoxa+/+ and Duoxa-/- mice between 3h and 24h. Duoxa-/- mice had significantly higher neutrophil influx 24h after LPS instillation despite similar cytokine levels (KC, MIP-2, or TGF-α) between the two groups. These findings suggest that LPS-TLR-4-induced KC or MIP-2 cytokine induction and subsequent neutrophil recruitment in the airway does not require DUOX-derived hydrogen peroxide from airway epithelium.
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spelling pubmed-44930232015-07-15 DUOX-Mediated Signaling Is Not Required for LPS-Induced Neutrophilic Response in the Airways Chang, Sandra Linderholm, Angela Harper, Richart PLoS One Research Article Oxidant production from DUOX1 has been proposed to lead to neutrophil recruitment into the airways when lung homeostasis is compromised. The objective of this study was to determine whether DUOX-derived hydrogen peroxide is required for LPS-induced neutrophil recruitment, using a functional DUOX knock out mouse model. We found that LPS induced profound neutrophilic lung inflammation in both Duoxa+/+ and Duoxa-/- mice between 3h and 24h. Duoxa-/- mice had significantly higher neutrophil influx 24h after LPS instillation despite similar cytokine levels (KC, MIP-2, or TGF-α) between the two groups. These findings suggest that LPS-TLR-4-induced KC or MIP-2 cytokine induction and subsequent neutrophil recruitment in the airway does not require DUOX-derived hydrogen peroxide from airway epithelium. Public Library of Science 2015-07-06 /pmc/articles/PMC4493023/ /pubmed/26148206 http://dx.doi.org/10.1371/journal.pone.0131810 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Chang, Sandra
Linderholm, Angela
Harper, Richart
DUOX-Mediated Signaling Is Not Required for LPS-Induced Neutrophilic Response in the Airways
title DUOX-Mediated Signaling Is Not Required for LPS-Induced Neutrophilic Response in the Airways
title_full DUOX-Mediated Signaling Is Not Required for LPS-Induced Neutrophilic Response in the Airways
title_fullStr DUOX-Mediated Signaling Is Not Required for LPS-Induced Neutrophilic Response in the Airways
title_full_unstemmed DUOX-Mediated Signaling Is Not Required for LPS-Induced Neutrophilic Response in the Airways
title_short DUOX-Mediated Signaling Is Not Required for LPS-Induced Neutrophilic Response in the Airways
title_sort duox-mediated signaling is not required for lps-induced neutrophilic response in the airways
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493023/
https://www.ncbi.nlm.nih.gov/pubmed/26148206
http://dx.doi.org/10.1371/journal.pone.0131810
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