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Temporal differentiation of bovine airway epithelial cells grown at an air-liquid interface

There is an urgent need to develop improved, physiologically-relevant in vitro models of airway epithelia with which to better understand the pathological processes associated with infection, allergies and toxicological insults of the respiratory tract of both humans and domesticated animals. In the...

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Autores principales: Cozens, Daniel, Sutherland, Erin, Marchesi, Francesco, Taylor, Geraldine, Berry, Catherine C., Davies, Robert L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6173764/
https://www.ncbi.nlm.nih.gov/pubmed/30291311
http://dx.doi.org/10.1038/s41598-018-33180-w
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author Cozens, Daniel
Sutherland, Erin
Marchesi, Francesco
Taylor, Geraldine
Berry, Catherine C.
Davies, Robert L.
author_facet Cozens, Daniel
Sutherland, Erin
Marchesi, Francesco
Taylor, Geraldine
Berry, Catherine C.
Davies, Robert L.
author_sort Cozens, Daniel
collection PubMed
description There is an urgent need to develop improved, physiologically-relevant in vitro models of airway epithelia with which to better understand the pathological processes associated with infection, allergies and toxicological insults of the respiratory tract of both humans and domesticated animals. In the present study, we have characterised the proliferation and differentiation of primary bovine bronchial epithelial cells (BBECs) grown at an air-liquid interface (ALI) at three-day intervals over a period of 42 days from the introduction of the ALI. The differentiated BBEC model was highly representative of the ex vivo epithelium from which the epithelial cells were derived; a columnar, pseudostratified epithelium that was highly reflective of native airway epithelium was formed which comprised ciliated, goblet and basal cells. The hallmark defences of the respiratory tract, namely barrier function and mucociliary clearance, were present, thus demonstrating that the model is an excellent mimic of bovine respiratory epithelium. The epithelium was fully differentiated by day 21 post-ALI and, crucially, remained healthy and stable for a further 21 days. Thus, the differentiated BBEC model has a three-week window which will allow wide-ranging and long-term experiments to be performed in the fields of infection, toxicology or general airway physiology.
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spelling pubmed-61737642018-10-09 Temporal differentiation of bovine airway epithelial cells grown at an air-liquid interface Cozens, Daniel Sutherland, Erin Marchesi, Francesco Taylor, Geraldine Berry, Catherine C. Davies, Robert L. Sci Rep Article There is an urgent need to develop improved, physiologically-relevant in vitro models of airway epithelia with which to better understand the pathological processes associated with infection, allergies and toxicological insults of the respiratory tract of both humans and domesticated animals. In the present study, we have characterised the proliferation and differentiation of primary bovine bronchial epithelial cells (BBECs) grown at an air-liquid interface (ALI) at three-day intervals over a period of 42 days from the introduction of the ALI. The differentiated BBEC model was highly representative of the ex vivo epithelium from which the epithelial cells were derived; a columnar, pseudostratified epithelium that was highly reflective of native airway epithelium was formed which comprised ciliated, goblet and basal cells. The hallmark defences of the respiratory tract, namely barrier function and mucociliary clearance, were present, thus demonstrating that the model is an excellent mimic of bovine respiratory epithelium. The epithelium was fully differentiated by day 21 post-ALI and, crucially, remained healthy and stable for a further 21 days. Thus, the differentiated BBEC model has a three-week window which will allow wide-ranging and long-term experiments to be performed in the fields of infection, toxicology or general airway physiology. Nature Publishing Group UK 2018-10-05 /pmc/articles/PMC6173764/ /pubmed/30291311 http://dx.doi.org/10.1038/s41598-018-33180-w Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Cozens, Daniel
Sutherland, Erin
Marchesi, Francesco
Taylor, Geraldine
Berry, Catherine C.
Davies, Robert L.
Temporal differentiation of bovine airway epithelial cells grown at an air-liquid interface
title Temporal differentiation of bovine airway epithelial cells grown at an air-liquid interface
title_full Temporal differentiation of bovine airway epithelial cells grown at an air-liquid interface
title_fullStr Temporal differentiation of bovine airway epithelial cells grown at an air-liquid interface
title_full_unstemmed Temporal differentiation of bovine airway epithelial cells grown at an air-liquid interface
title_short Temporal differentiation of bovine airway epithelial cells grown at an air-liquid interface
title_sort temporal differentiation of bovine airway epithelial cells grown at an air-liquid interface
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6173764/
https://www.ncbi.nlm.nih.gov/pubmed/30291311
http://dx.doi.org/10.1038/s41598-018-33180-w
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