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Dynamic evolution of emphysema and airway remodeling in two mouse models of COPD
BACKGROUND: Establishment of a mouse model is important for investigating the mechanism of chronic obstructive pulmonary disease (COPD). In this study, we observed and compared the evolution of the pathology in two mouse models of COPD induced by cigarette smoke (CS) exposure alone or in combination...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073949/ https://www.ncbi.nlm.nih.gov/pubmed/33902528 http://dx.doi.org/10.1186/s12890-021-01456-z |
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author | Yang, Yue Di, Tingting Zhang, Zixiao Liu, Jiaxin Fu, Congli Wu, Yan Bian, Tao |
author_facet | Yang, Yue Di, Tingting Zhang, Zixiao Liu, Jiaxin Fu, Congli Wu, Yan Bian, Tao |
author_sort | Yang, Yue |
collection | PubMed |
description | BACKGROUND: Establishment of a mouse model is important for investigating the mechanism of chronic obstructive pulmonary disease (COPD). In this study, we observed and compared the evolution of the pathology in two mouse models of COPD induced by cigarette smoke (CS) exposure alone or in combination with lipopolysaccharide (LPS). METHODS: One hundred eight wild-type C57BL/6 mice were equally divided into three groups: the (1) control group, (2) CS-exposed group (CS group), and (3) CS + LPS-exposed group (CS + LPS group). The body weight of the mice was recorded, and noninvasive lung function tests were performed monthly. Inflammation was evaluated by counting the number of inflammatory cells in bronchoalveolar lavage fluid and measuring the expression of the IL-6 mRNA in mouse lung tissue. Changes in pathology were assessed by performing hematoxylin and eosin and Masson staining of lung tissue sections. RESULTS: The two treatments induced emphysema and airway remodeling and decreased lung function. Emphysema was induced after 1 month of exposure to CS or CS + LPS, while airway remodeling was induced after 2 months of exposure to CS + LPS and 3 months of exposure to CS. Moreover, the mice in the CS + LPS group exhibited more severe inflammation and airway remodeling than the mice in the CS group, but the two treatments induced similar levels of emphysema. CONCLUSION: Compared with the single CS exposure method, the CS + LPS exposure method is a more suitable model of COPD in airway remodeling research. Conversely, the CS exposure method is a more suitable model of COPD for emphysema research due to its simple operation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12890-021-01456-z. |
format | Online Article Text |
id | pubmed-8073949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80739492021-04-26 Dynamic evolution of emphysema and airway remodeling in two mouse models of COPD Yang, Yue Di, Tingting Zhang, Zixiao Liu, Jiaxin Fu, Congli Wu, Yan Bian, Tao BMC Pulm Med Research BACKGROUND: Establishment of a mouse model is important for investigating the mechanism of chronic obstructive pulmonary disease (COPD). In this study, we observed and compared the evolution of the pathology in two mouse models of COPD induced by cigarette smoke (CS) exposure alone or in combination with lipopolysaccharide (LPS). METHODS: One hundred eight wild-type C57BL/6 mice were equally divided into three groups: the (1) control group, (2) CS-exposed group (CS group), and (3) CS + LPS-exposed group (CS + LPS group). The body weight of the mice was recorded, and noninvasive lung function tests were performed monthly. Inflammation was evaluated by counting the number of inflammatory cells in bronchoalveolar lavage fluid and measuring the expression of the IL-6 mRNA in mouse lung tissue. Changes in pathology were assessed by performing hematoxylin and eosin and Masson staining of lung tissue sections. RESULTS: The two treatments induced emphysema and airway remodeling and decreased lung function. Emphysema was induced after 1 month of exposure to CS or CS + LPS, while airway remodeling was induced after 2 months of exposure to CS + LPS and 3 months of exposure to CS. Moreover, the mice in the CS + LPS group exhibited more severe inflammation and airway remodeling than the mice in the CS group, but the two treatments induced similar levels of emphysema. CONCLUSION: Compared with the single CS exposure method, the CS + LPS exposure method is a more suitable model of COPD in airway remodeling research. Conversely, the CS exposure method is a more suitable model of COPD for emphysema research due to its simple operation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12890-021-01456-z. BioMed Central 2021-04-26 /pmc/articles/PMC8073949/ /pubmed/33902528 http://dx.doi.org/10.1186/s12890-021-01456-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Yang, Yue Di, Tingting Zhang, Zixiao Liu, Jiaxin Fu, Congli Wu, Yan Bian, Tao Dynamic evolution of emphysema and airway remodeling in two mouse models of COPD |
title | Dynamic evolution of emphysema and airway remodeling in two mouse models of COPD |
title_full | Dynamic evolution of emphysema and airway remodeling in two mouse models of COPD |
title_fullStr | Dynamic evolution of emphysema and airway remodeling in two mouse models of COPD |
title_full_unstemmed | Dynamic evolution of emphysema and airway remodeling in two mouse models of COPD |
title_short | Dynamic evolution of emphysema and airway remodeling in two mouse models of COPD |
title_sort | dynamic evolution of emphysema and airway remodeling in two mouse models of copd |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8073949/ https://www.ncbi.nlm.nih.gov/pubmed/33902528 http://dx.doi.org/10.1186/s12890-021-01456-z |
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