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Cytotoxicity and Induction of Inflammation by Pepsin in Acid in Bronchial Epithelial Cells
Introduction. Gastroesophageal reflux has been associated with chronic inflammatory diseases and may be a cause of airway remodelling. Aspiration of gastric fluids may cause damage to airway epithelial cells, not only because acidity is toxic to bronchial epithelial cells, but also since it contains...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE-Hindawi Access to Research
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3139191/ https://www.ncbi.nlm.nih.gov/pubmed/21785693 http://dx.doi.org/10.4061/2011/569416 |
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author | Bathoorn, Erik Daly, Paul Gaiser, Birgit Sternad, Karl Poland, Craig MacNee, William Drost, Ellen M. |
author_facet | Bathoorn, Erik Daly, Paul Gaiser, Birgit Sternad, Karl Poland, Craig MacNee, William Drost, Ellen M. |
author_sort | Bathoorn, Erik |
collection | PubMed |
description | Introduction. Gastroesophageal reflux has been associated with chronic inflammatory diseases and may be a cause of airway remodelling. Aspiration of gastric fluids may cause damage to airway epithelial cells, not only because acidity is toxic to bronchial epithelial cells, but also since it contains digestive enzymes, such as pepsin. Aim. To study whether pepsin enhances cytotoxicity and inflammation in airway epithelial cells, and whether this is pH-dependent. Methods. Human bronchial epithelial cells were exposed to increasing pepsin concentrations in varying acidic milieus, and cell proliferation and cytokine release were assessed. Results. Cell survival was decreased by pepsin exposure depending on its concentration (F = 17.4) and pH level of the medium (F = 6.5) (both P < 0.01). Pepsin-induced interleukin-8 release was greater at lower pH (F = 5.1; P < 0.01). Interleukin-6 induction by pepsin was greater at pH 1.5 compared to pH 2.5 (mean difference 434%; P = 0.03). Conclusion. Pepsin is cytotoxic to bronchial epithelial cells and induces inflammation in addition to acid alone, dependent on the level of acidity. Future studies should assess whether chronic aspiration causes airway remodelling in chronic inflammatory lung diseases. |
format | Online Article Text |
id | pubmed-3139191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | SAGE-Hindawi Access to Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-31391912011-07-22 Cytotoxicity and Induction of Inflammation by Pepsin in Acid in Bronchial Epithelial Cells Bathoorn, Erik Daly, Paul Gaiser, Birgit Sternad, Karl Poland, Craig MacNee, William Drost, Ellen M. Int J Inflam Research Article Introduction. Gastroesophageal reflux has been associated with chronic inflammatory diseases and may be a cause of airway remodelling. Aspiration of gastric fluids may cause damage to airway epithelial cells, not only because acidity is toxic to bronchial epithelial cells, but also since it contains digestive enzymes, such as pepsin. Aim. To study whether pepsin enhances cytotoxicity and inflammation in airway epithelial cells, and whether this is pH-dependent. Methods. Human bronchial epithelial cells were exposed to increasing pepsin concentrations in varying acidic milieus, and cell proliferation and cytokine release were assessed. Results. Cell survival was decreased by pepsin exposure depending on its concentration (F = 17.4) and pH level of the medium (F = 6.5) (both P < 0.01). Pepsin-induced interleukin-8 release was greater at lower pH (F = 5.1; P < 0.01). Interleukin-6 induction by pepsin was greater at pH 1.5 compared to pH 2.5 (mean difference 434%; P = 0.03). Conclusion. Pepsin is cytotoxic to bronchial epithelial cells and induces inflammation in addition to acid alone, dependent on the level of acidity. Future studies should assess whether chronic aspiration causes airway remodelling in chronic inflammatory lung diseases. SAGE-Hindawi Access to Research 2011-07-12 /pmc/articles/PMC3139191/ /pubmed/21785693 http://dx.doi.org/10.4061/2011/569416 Text en Copyright © 2011 Erik Bathoorn et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bathoorn, Erik Daly, Paul Gaiser, Birgit Sternad, Karl Poland, Craig MacNee, William Drost, Ellen M. Cytotoxicity and Induction of Inflammation by Pepsin in Acid in Bronchial Epithelial Cells |
title | Cytotoxicity and Induction of Inflammation by Pepsin in Acid in Bronchial Epithelial Cells |
title_full | Cytotoxicity and Induction of Inflammation by Pepsin in Acid in Bronchial Epithelial Cells |
title_fullStr | Cytotoxicity and Induction of Inflammation by Pepsin in Acid in Bronchial Epithelial Cells |
title_full_unstemmed | Cytotoxicity and Induction of Inflammation by Pepsin in Acid in Bronchial Epithelial Cells |
title_short | Cytotoxicity and Induction of Inflammation by Pepsin in Acid in Bronchial Epithelial Cells |
title_sort | cytotoxicity and induction of inflammation by pepsin in acid in bronchial epithelial cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3139191/ https://www.ncbi.nlm.nih.gov/pubmed/21785693 http://dx.doi.org/10.4061/2011/569416 |
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