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Animal models of acute exacerbation of pulmonary fibrosis
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive scarring interstitial lung disease with an unknown cause. Some patients may experience acute exacerbations (AE), which result in severe lung damage visible on imaging or through examination of tissue samples, often leading to high mortali...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675932/ https://www.ncbi.nlm.nih.gov/pubmed/38007420 http://dx.doi.org/10.1186/s12931-023-02595-z |
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author | Ye, Xu Zhang, Mingrui Gu, Huimin Liu, Mengying Zhao, Yichao Shi, Yanchen Wu, Shufei Jiang, Cheng Ye, Xiaoling Zhu, Huihui Li, Qi Huang, Xinmei Cao, Mengshu |
author_facet | Ye, Xu Zhang, Mingrui Gu, Huimin Liu, Mengying Zhao, Yichao Shi, Yanchen Wu, Shufei Jiang, Cheng Ye, Xiaoling Zhu, Huihui Li, Qi Huang, Xinmei Cao, Mengshu |
author_sort | Ye, Xu |
collection | PubMed |
description | Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive scarring interstitial lung disease with an unknown cause. Some patients may experience acute exacerbations (AE), which result in severe lung damage visible on imaging or through examination of tissue samples, often leading to high mortality rates. However, the etiology and pathogenesis of AE-IPF remain unclear. AE-IPF patients exhibit diffuse lung damage, apoptosis of type II alveolar epithelial cells, and an excessive inflammatory response. Establishing a reliable animal model of AE is critical for investigating the pathogenesis. Recent studies have reported a variety of animal models for AE-IPF, each with its own advantages and disadvantages. These models are usually established in mice with bleomycin-induced pulmonary fibrosis, using viruses, bacteria, small peptides, or specific drugs. In this review, we present an overview of different AE models, hoping to provide a useful resource for exploring the mechanisms and targeted therapies for AE-IPF. |
format | Online Article Text |
id | pubmed-10675932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106759322023-11-25 Animal models of acute exacerbation of pulmonary fibrosis Ye, Xu Zhang, Mingrui Gu, Huimin Liu, Mengying Zhao, Yichao Shi, Yanchen Wu, Shufei Jiang, Cheng Ye, Xiaoling Zhu, Huihui Li, Qi Huang, Xinmei Cao, Mengshu Respir Res Review Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive scarring interstitial lung disease with an unknown cause. Some patients may experience acute exacerbations (AE), which result in severe lung damage visible on imaging or through examination of tissue samples, often leading to high mortality rates. However, the etiology and pathogenesis of AE-IPF remain unclear. AE-IPF patients exhibit diffuse lung damage, apoptosis of type II alveolar epithelial cells, and an excessive inflammatory response. Establishing a reliable animal model of AE is critical for investigating the pathogenesis. Recent studies have reported a variety of animal models for AE-IPF, each with its own advantages and disadvantages. These models are usually established in mice with bleomycin-induced pulmonary fibrosis, using viruses, bacteria, small peptides, or specific drugs. In this review, we present an overview of different AE models, hoping to provide a useful resource for exploring the mechanisms and targeted therapies for AE-IPF. BioMed Central 2023-11-25 2023 /pmc/articles/PMC10675932/ /pubmed/38007420 http://dx.doi.org/10.1186/s12931-023-02595-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 | Review Ye, Xu Zhang, Mingrui Gu, Huimin Liu, Mengying Zhao, Yichao Shi, Yanchen Wu, Shufei Jiang, Cheng Ye, Xiaoling Zhu, Huihui Li, Qi Huang, Xinmei Cao, Mengshu Animal models of acute exacerbation of pulmonary fibrosis |
title | Animal models of acute exacerbation of pulmonary fibrosis |
title_full | Animal models of acute exacerbation of pulmonary fibrosis |
title_fullStr | Animal models of acute exacerbation of pulmonary fibrosis |
title_full_unstemmed | Animal models of acute exacerbation of pulmonary fibrosis |
title_short | Animal models of acute exacerbation of pulmonary fibrosis |
title_sort | animal models of acute exacerbation of pulmonary fibrosis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675932/ https://www.ncbi.nlm.nih.gov/pubmed/38007420 http://dx.doi.org/10.1186/s12931-023-02595-z |
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