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Critical role of tumor necrosis factor receptor 1 in the pathogenesis of pulmonary emphysema in mice
COPD is a major cause of chronic morbidity and mortality throughout the world. Although tumor necrosis factor-α (TNF-α) has a critical role in the development of COPD, the role of different TNF receptors (TNFRs) in pulmonary emphysema has not been resolved. We aimed to clarify the role of TNFRs in t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968668/ https://www.ncbi.nlm.nih.gov/pubmed/27555760 http://dx.doi.org/10.2147/COPD.S108919 |
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author | Fujita, Masaki Ouchi, Hiroshi Ikegame, Satoshi Harada, Eiji Matsumoto, Takemasa Uchino, Junji Nakanishi, Yoichi Watanabe, Kentaro |
author_facet | Fujita, Masaki Ouchi, Hiroshi Ikegame, Satoshi Harada, Eiji Matsumoto, Takemasa Uchino, Junji Nakanishi, Yoichi Watanabe, Kentaro |
author_sort | Fujita, Masaki |
collection | PubMed |
description | COPD is a major cause of chronic morbidity and mortality throughout the world. Although tumor necrosis factor-α (TNF-α) has a critical role in the development of COPD, the role of different TNF receptors (TNFRs) in pulmonary emphysema has not been resolved. We aimed to clarify the role of TNFRs in the development of pulmonary emphysema. TNF-α transgenic mice, a murine model of COPD in which the mice spontaneously develop emphysema with a large increase in lung volume and pulmonary hypertension, were crossed with either TNFR1-deficient mice or TNFR2-deficient mice. After 6 months, the gross appearance of the lung, lung histology, and pulmonary and cardiac physiology were determined. In addition, the relationship between apoptosis and emphysema was investigated. Pulmonary emphysema-like changes disappeared with deletion of TNFR1. However, slight improvements were attained with deletion of TNFR2. Apoptotic cells in the interstitium of the lung were observed in TNF-α transgenic mice. The apoptotic signals through TNFR1 appear critical for the pathogenesis of pulmonary emphysema. In contrast, the inflammatory process has a less important role for the development of emphysema. |
format | Online Article Text |
id | pubmed-4968668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49686682016-08-23 Critical role of tumor necrosis factor receptor 1 in the pathogenesis of pulmonary emphysema in mice Fujita, Masaki Ouchi, Hiroshi Ikegame, Satoshi Harada, Eiji Matsumoto, Takemasa Uchino, Junji Nakanishi, Yoichi Watanabe, Kentaro Int J Chron Obstruct Pulmon Dis Original Research COPD is a major cause of chronic morbidity and mortality throughout the world. Although tumor necrosis factor-α (TNF-α) has a critical role in the development of COPD, the role of different TNF receptors (TNFRs) in pulmonary emphysema has not been resolved. We aimed to clarify the role of TNFRs in the development of pulmonary emphysema. TNF-α transgenic mice, a murine model of COPD in which the mice spontaneously develop emphysema with a large increase in lung volume and pulmonary hypertension, were crossed with either TNFR1-deficient mice or TNFR2-deficient mice. After 6 months, the gross appearance of the lung, lung histology, and pulmonary and cardiac physiology were determined. In addition, the relationship between apoptosis and emphysema was investigated. Pulmonary emphysema-like changes disappeared with deletion of TNFR1. However, slight improvements were attained with deletion of TNFR2. Apoptotic cells in the interstitium of the lung were observed in TNF-α transgenic mice. The apoptotic signals through TNFR1 appear critical for the pathogenesis of pulmonary emphysema. In contrast, the inflammatory process has a less important role for the development of emphysema. Dove Medical Press 2016-07-28 /pmc/articles/PMC4968668/ /pubmed/27555760 http://dx.doi.org/10.2147/COPD.S108919 Text en © 2016 Fujita et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Fujita, Masaki Ouchi, Hiroshi Ikegame, Satoshi Harada, Eiji Matsumoto, Takemasa Uchino, Junji Nakanishi, Yoichi Watanabe, Kentaro Critical role of tumor necrosis factor receptor 1 in the pathogenesis of pulmonary emphysema in mice |
title | Critical role of tumor necrosis factor receptor 1 in the pathogenesis of pulmonary emphysema in mice |
title_full | Critical role of tumor necrosis factor receptor 1 in the pathogenesis of pulmonary emphysema in mice |
title_fullStr | Critical role of tumor necrosis factor receptor 1 in the pathogenesis of pulmonary emphysema in mice |
title_full_unstemmed | Critical role of tumor necrosis factor receptor 1 in the pathogenesis of pulmonary emphysema in mice |
title_short | Critical role of tumor necrosis factor receptor 1 in the pathogenesis of pulmonary emphysema in mice |
title_sort | critical role of tumor necrosis factor receptor 1 in the pathogenesis of pulmonary emphysema in mice |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968668/ https://www.ncbi.nlm.nih.gov/pubmed/27555760 http://dx.doi.org/10.2147/COPD.S108919 |
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