Cargando…

Connexin 43 Upregulation in Mouse Lungs during Ovalbumin-Induced Asthma

BACKGROUND: Connexin (Cx)-based gap junction channels play important roles in the inflammatory response. Cx43 is involved in the pathogenesis of some lung diseases such as acute lung injury. However, the Cx43 expression in asthma is unclear. In the present study, we used a murine model of ovalbumin...

Descripción completa

Detalles Bibliográficos
Autores principales: Yao, Yin, Zeng, Qing-Xiang, Deng, Xue-Quan, Tang, Guan-Nan, Guo, Jie-Bo, Sun, Yue-Qi, Ru, Kun, Rizzo, Alicia N., Shi, Jian-Bo, Fu, Qing-Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667899/
https://www.ncbi.nlm.nih.gov/pubmed/26630490
http://dx.doi.org/10.1371/journal.pone.0144106
_version_ 1782403897687539712
author Yao, Yin
Zeng, Qing-Xiang
Deng, Xue-Quan
Tang, Guan-Nan
Guo, Jie-Bo
Sun, Yue-Qi
Ru, Kun
Rizzo, Alicia N.
Shi, Jian-Bo
Fu, Qing-Ling
author_facet Yao, Yin
Zeng, Qing-Xiang
Deng, Xue-Quan
Tang, Guan-Nan
Guo, Jie-Bo
Sun, Yue-Qi
Ru, Kun
Rizzo, Alicia N.
Shi, Jian-Bo
Fu, Qing-Ling
author_sort Yao, Yin
collection PubMed
description BACKGROUND: Connexin (Cx)-based gap junction channels play important roles in the inflammatory response. Cx43 is involved in the pathogenesis of some lung diseases such as acute lung injury. However, the Cx43 expression in asthma is unclear. In the present study, we used a murine model of ovalbumin (OVA)-induced allergic airway disease to examine the levels of Cx43 and analyze the relationship between Cx43 and airway inflammation in allergic airway disease. METHODS: Asthma was induced in mice via sensitization and challenge with OVA. Cx43 mRNA and protein expression levels were investigated via QT-PCR, western blot, and immunohistochemistry 0 h, 8 h, 1 d, 2 d and 4 d after the first challenge. The relationship between Cx43 protein levels and inflammatory cell infiltration, cytokine levels was analyzed. RESULTS: The OVA-induced mice exhibited typical pathological features of asthma, including airway hyper-responsiveness; strong inflammatory cell infiltration surrounding the bronchia and vessels; many inflammatory cells in the bronchoalveolar lavage fluid (BALF); higher IL-4, IL-5 and IL-13 levels; and high OVA specific IgE levels. Low Cx43 expression was detected in the lungs of control (PBS) mice. A dramatic increase in the Cx43 mRNA and protein levels was found in the asthmatic mice. Cx43 mRNA and protein expression levels increased in a time-dependent manner in asthma mice, and Cx43 was mostly localized in the alveolar and bronchial epithelial layers. Moreover, lung Cx43 protein levels showed a significant positive correlation with inflammatory cell infiltration in the airway and IL-4 and IL-5 levels in the BALF at different time points after challenge. Interestingly, the increase in Cx43 mRNA and protein levels occurred prior to the appearance of the inflammatory cell infiltration. CONCLUSION: Our data suggest that there is a strong upregulation of Cx43 mRNA and protein levels in the lungs in asthma. Cx43 levels also exhibited a positive correlation with allergic airway inflammation. Cx43 may represent a target to treat allergic airway diseases in the future.
format Online
Article
Text
id pubmed-4667899
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-46678992015-12-10 Connexin 43 Upregulation in Mouse Lungs during Ovalbumin-Induced Asthma Yao, Yin Zeng, Qing-Xiang Deng, Xue-Quan Tang, Guan-Nan Guo, Jie-Bo Sun, Yue-Qi Ru, Kun Rizzo, Alicia N. Shi, Jian-Bo Fu, Qing-Ling PLoS One Research Article BACKGROUND: Connexin (Cx)-based gap junction channels play important roles in the inflammatory response. Cx43 is involved in the pathogenesis of some lung diseases such as acute lung injury. However, the Cx43 expression in asthma is unclear. In the present study, we used a murine model of ovalbumin (OVA)-induced allergic airway disease to examine the levels of Cx43 and analyze the relationship between Cx43 and airway inflammation in allergic airway disease. METHODS: Asthma was induced in mice via sensitization and challenge with OVA. Cx43 mRNA and protein expression levels were investigated via QT-PCR, western blot, and immunohistochemistry 0 h, 8 h, 1 d, 2 d and 4 d after the first challenge. The relationship between Cx43 protein levels and inflammatory cell infiltration, cytokine levels was analyzed. RESULTS: The OVA-induced mice exhibited typical pathological features of asthma, including airway hyper-responsiveness; strong inflammatory cell infiltration surrounding the bronchia and vessels; many inflammatory cells in the bronchoalveolar lavage fluid (BALF); higher IL-4, IL-5 and IL-13 levels; and high OVA specific IgE levels. Low Cx43 expression was detected in the lungs of control (PBS) mice. A dramatic increase in the Cx43 mRNA and protein levels was found in the asthmatic mice. Cx43 mRNA and protein expression levels increased in a time-dependent manner in asthma mice, and Cx43 was mostly localized in the alveolar and bronchial epithelial layers. Moreover, lung Cx43 protein levels showed a significant positive correlation with inflammatory cell infiltration in the airway and IL-4 and IL-5 levels in the BALF at different time points after challenge. Interestingly, the increase in Cx43 mRNA and protein levels occurred prior to the appearance of the inflammatory cell infiltration. CONCLUSION: Our data suggest that there is a strong upregulation of Cx43 mRNA and protein levels in the lungs in asthma. Cx43 levels also exhibited a positive correlation with allergic airway inflammation. Cx43 may represent a target to treat allergic airway diseases in the future. Public Library of Science 2015-12-02 /pmc/articles/PMC4667899/ /pubmed/26630490 http://dx.doi.org/10.1371/journal.pone.0144106 Text en © 2015 Yao 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Yao, Yin
Zeng, Qing-Xiang
Deng, Xue-Quan
Tang, Guan-Nan
Guo, Jie-Bo
Sun, Yue-Qi
Ru, Kun
Rizzo, Alicia N.
Shi, Jian-Bo
Fu, Qing-Ling
Connexin 43 Upregulation in Mouse Lungs during Ovalbumin-Induced Asthma
title Connexin 43 Upregulation in Mouse Lungs during Ovalbumin-Induced Asthma
title_full Connexin 43 Upregulation in Mouse Lungs during Ovalbumin-Induced Asthma
title_fullStr Connexin 43 Upregulation in Mouse Lungs during Ovalbumin-Induced Asthma
title_full_unstemmed Connexin 43 Upregulation in Mouse Lungs during Ovalbumin-Induced Asthma
title_short Connexin 43 Upregulation in Mouse Lungs during Ovalbumin-Induced Asthma
title_sort connexin 43 upregulation in mouse lungs during ovalbumin-induced asthma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667899/
https://www.ncbi.nlm.nih.gov/pubmed/26630490
http://dx.doi.org/10.1371/journal.pone.0144106
work_keys_str_mv AT yaoyin connexin43upregulationinmouselungsduringovalbumininducedasthma
AT zengqingxiang connexin43upregulationinmouselungsduringovalbumininducedasthma
AT dengxuequan connexin43upregulationinmouselungsduringovalbumininducedasthma
AT tangguannan connexin43upregulationinmouselungsduringovalbumininducedasthma
AT guojiebo connexin43upregulationinmouselungsduringovalbumininducedasthma
AT sunyueqi connexin43upregulationinmouselungsduringovalbumininducedasthma
AT rukun connexin43upregulationinmouselungsduringovalbumininducedasthma
AT rizzoalician connexin43upregulationinmouselungsduringovalbumininducedasthma
AT shijianbo connexin43upregulationinmouselungsduringovalbumininducedasthma
AT fuqingling connexin43upregulationinmouselungsduringovalbumininducedasthma