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Reassessment of the importance of mucins in determining sputum properties in cystic fibrosis
BACKGROUND: There is conflicting evidence about the importance of airway mucins (MUC5AC and MUC5B) in determining physical properties of sputum in cystic fibrosis (CF). We studied the effects of endogenous degradation of mucins on CF sputum elasticity and apparent mucin concentrations. METHODS: Elas...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994278/ https://www.ncbi.nlm.nih.gov/pubmed/24332705 http://dx.doi.org/10.1016/j.jcf.2013.11.002 |
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author | Horsley, Alex Rousseau, Karine Ridley, Caroline Flight, William Jones, Andrew Waigh, Thomas A. Thornton, David J. |
author_facet | Horsley, Alex Rousseau, Karine Ridley, Caroline Flight, William Jones, Andrew Waigh, Thomas A. Thornton, David J. |
author_sort | Horsley, Alex |
collection | PubMed |
description | BACKGROUND: There is conflicting evidence about the importance of airway mucins (MUC5AC and MUC5B) in determining physical properties of sputum in cystic fibrosis (CF). We studied the effects of endogenous degradation of mucins on CF sputum elasticity and apparent mucin concentrations. METHODS: Elastic shear moduli (G′) and mucin concentrations in sputum of 12 CF patients were measured before and after incubation at 37 °C for 60 min. RESULTS: G′ fell from a median of 5.98 to 4.70 Pa (p = 0.01). There were significant falls in MUC5AC (8.2 to 5.2 μg/ml, p = 0.02) and MUC5B (17.3 to 12.5 μg/ml, p = 0.02) over the same period, and associated decrease in molecular weight and size. CONCLUSIONS: Sputum is not inert and degradation reduces apparent mucin concentrations and sputum elasticity. Even if care is taken to process samples rapidly, sputum may therefore differ from secretions retained in airways. Previous studies may have underestimated the role of mucins in CF sputum. |
format | Online Article Text |
id | pubmed-3994278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-39942782014-05-01 Reassessment of the importance of mucins in determining sputum properties in cystic fibrosis Horsley, Alex Rousseau, Karine Ridley, Caroline Flight, William Jones, Andrew Waigh, Thomas A. Thornton, David J. J Cyst Fibros Original Article BACKGROUND: There is conflicting evidence about the importance of airway mucins (MUC5AC and MUC5B) in determining physical properties of sputum in cystic fibrosis (CF). We studied the effects of endogenous degradation of mucins on CF sputum elasticity and apparent mucin concentrations. METHODS: Elastic shear moduli (G′) and mucin concentrations in sputum of 12 CF patients were measured before and after incubation at 37 °C for 60 min. RESULTS: G′ fell from a median of 5.98 to 4.70 Pa (p = 0.01). There were significant falls in MUC5AC (8.2 to 5.2 μg/ml, p = 0.02) and MUC5B (17.3 to 12.5 μg/ml, p = 0.02) over the same period, and associated decrease in molecular weight and size. CONCLUSIONS: Sputum is not inert and degradation reduces apparent mucin concentrations and sputum elasticity. Even if care is taken to process samples rapidly, sputum may therefore differ from secretions retained in airways. Previous studies may have underestimated the role of mucins in CF sputum. Elsevier 2014-05 /pmc/articles/PMC3994278/ /pubmed/24332705 http://dx.doi.org/10.1016/j.jcf.2013.11.002 Text en © 2013 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved. https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Original Article Horsley, Alex Rousseau, Karine Ridley, Caroline Flight, William Jones, Andrew Waigh, Thomas A. Thornton, David J. Reassessment of the importance of mucins in determining sputum properties in cystic fibrosis |
title | Reassessment of the importance of mucins in determining sputum properties in cystic fibrosis |
title_full | Reassessment of the importance of mucins in determining sputum properties in cystic fibrosis |
title_fullStr | Reassessment of the importance of mucins in determining sputum properties in cystic fibrosis |
title_full_unstemmed | Reassessment of the importance of mucins in determining sputum properties in cystic fibrosis |
title_short | Reassessment of the importance of mucins in determining sputum properties in cystic fibrosis |
title_sort | reassessment of the importance of mucins in determining sputum properties in cystic fibrosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994278/ https://www.ncbi.nlm.nih.gov/pubmed/24332705 http://dx.doi.org/10.1016/j.jcf.2013.11.002 |
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