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Alcohol-Induced Mucociliary Dysfunction: Role of Defective CFTR Channel Function
Excessive alcohol use is thought to increase the risk of respiratory infections by impairing mucociliary clearance (MCC). In this study, we investigate the hypothesis that alcohol reduces the function of CFTR, the protein that is defective in individuals with cystic fibrosis, thus altering mucus pro...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370077/ https://www.ncbi.nlm.nih.gov/pubmed/37502889 http://dx.doi.org/10.1101/2023.07.17.548927 |
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author | Rasmussen, Lawrence Stafford, Denise LaFontaine, Jennifer Allen, Antonio Antony, Linto Kim, Hyunki Raju, S. Vamsee |
author_facet | Rasmussen, Lawrence Stafford, Denise LaFontaine, Jennifer Allen, Antonio Antony, Linto Kim, Hyunki Raju, S. Vamsee |
author_sort | Rasmussen, Lawrence |
collection | PubMed |
description | Excessive alcohol use is thought to increase the risk of respiratory infections by impairing mucociliary clearance (MCC). In this study, we investigate the hypothesis that alcohol reduces the function of CFTR, the protein that is defective in individuals with cystic fibrosis, thus altering mucus properties to impair MCC and the airway’s defense against inhaled pathogens. METHODS: Sprague Dawley rats with wild type CFTR (+/+), matched for age and sex, were administered either a Lieber-DeCarli alcohol diet or a control diet with the same number of calories for eight weeks. CFTR activity was measured using nasal potential difference (NPD) assay and Ussing chamber electrophysiology of tracheal tissue samples. In vivo MCC was determined by measuring the radiographic clearance of inhaled Tc99 particles and the depth of the airway periciliary liquid (PCL) and mucus transport rate in excised trachea using micro-optical coherence tomography (μOCT). The levels of rat lung MUC5b and CFTR were estimated by protein and mRNA analysis. RESULTS: Alcohol diet was found to decrease CFTR ion transport in the nasal and tracheal epithelium in vivo and ex vivo. This decrease in activity was also reflected in partially reduced full-length CFTR protein levels but not, in mRNA copies, in the lungs of rats. Furthermore, alcohol-fed rats showed a significant decrease in MCC after 8 weeks of alcohol consumption. The trachea from these rats also showed reduced PCL depth, indicating a decrease in mucosal surface hydration that was reflected in delayed mucus transport. Diminished MCC rate was also likely due to the elevated MUC5b expression in alcohol-fed rat lungs. CONCLUSIONS: Excessive alcohol use can decrease the expression and activity of CFTR channels, leading to reduced airway surface hydration and impaired mucus clearance. This suggests that CFTR dysfunction plays a role in the compromised lung defense against respiratory pathogens in individuals who drink alcohol excessively. |
format | Online Article Text |
id | pubmed-10370077 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-103700772023-07-27 Alcohol-Induced Mucociliary Dysfunction: Role of Defective CFTR Channel Function Rasmussen, Lawrence Stafford, Denise LaFontaine, Jennifer Allen, Antonio Antony, Linto Kim, Hyunki Raju, S. Vamsee bioRxiv Article Excessive alcohol use is thought to increase the risk of respiratory infections by impairing mucociliary clearance (MCC). In this study, we investigate the hypothesis that alcohol reduces the function of CFTR, the protein that is defective in individuals with cystic fibrosis, thus altering mucus properties to impair MCC and the airway’s defense against inhaled pathogens. METHODS: Sprague Dawley rats with wild type CFTR (+/+), matched for age and sex, were administered either a Lieber-DeCarli alcohol diet or a control diet with the same number of calories for eight weeks. CFTR activity was measured using nasal potential difference (NPD) assay and Ussing chamber electrophysiology of tracheal tissue samples. In vivo MCC was determined by measuring the radiographic clearance of inhaled Tc99 particles and the depth of the airway periciliary liquid (PCL) and mucus transport rate in excised trachea using micro-optical coherence tomography (μOCT). The levels of rat lung MUC5b and CFTR were estimated by protein and mRNA analysis. RESULTS: Alcohol diet was found to decrease CFTR ion transport in the nasal and tracheal epithelium in vivo and ex vivo. This decrease in activity was also reflected in partially reduced full-length CFTR protein levels but not, in mRNA copies, in the lungs of rats. Furthermore, alcohol-fed rats showed a significant decrease in MCC after 8 weeks of alcohol consumption. The trachea from these rats also showed reduced PCL depth, indicating a decrease in mucosal surface hydration that was reflected in delayed mucus transport. Diminished MCC rate was also likely due to the elevated MUC5b expression in alcohol-fed rat lungs. CONCLUSIONS: Excessive alcohol use can decrease the expression and activity of CFTR channels, leading to reduced airway surface hydration and impaired mucus clearance. This suggests that CFTR dysfunction plays a role in the compromised lung defense against respiratory pathogens in individuals who drink alcohol excessively. Cold Spring Harbor Laboratory 2023-07-19 /pmc/articles/PMC10370077/ /pubmed/37502889 http://dx.doi.org/10.1101/2023.07.17.548927 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Rasmussen, Lawrence Stafford, Denise LaFontaine, Jennifer Allen, Antonio Antony, Linto Kim, Hyunki Raju, S. Vamsee Alcohol-Induced Mucociliary Dysfunction: Role of Defective CFTR Channel Function |
title | Alcohol-Induced Mucociliary Dysfunction: Role of Defective CFTR Channel Function |
title_full | Alcohol-Induced Mucociliary Dysfunction: Role of Defective CFTR Channel Function |
title_fullStr | Alcohol-Induced Mucociliary Dysfunction: Role of Defective CFTR Channel Function |
title_full_unstemmed | Alcohol-Induced Mucociliary Dysfunction: Role of Defective CFTR Channel Function |
title_short | Alcohol-Induced Mucociliary Dysfunction: Role of Defective CFTR Channel Function |
title_sort | alcohol-induced mucociliary dysfunction: role of defective cftr channel function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370077/ https://www.ncbi.nlm.nih.gov/pubmed/37502889 http://dx.doi.org/10.1101/2023.07.17.548927 |
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