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An in vitro model of murine middle ear epithelium

Otitis media (OM), or middle ear inflammation, is the most common paediatric disease and leads to significant morbidity. Although understanding of underlying disease mechanisms is hampered by complex pathophysiology it is clear that epithelial abnormalities underpin the disease. There is currently a...

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Autores principales: Mulay, Apoorva, Akram, Khondoker M., Williams, Debbie, Armes, Hannah, Russell, Catherine, Hood, Derek, Armstrong, Stuart, Stewart, James P., Brown, Steve D. M., Bingle, Lynne, Bingle, Colin D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117233/
https://www.ncbi.nlm.nih.gov/pubmed/27660200
http://dx.doi.org/10.1242/dmm.026658
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author Mulay, Apoorva
Akram, Khondoker M.
Williams, Debbie
Armes, Hannah
Russell, Catherine
Hood, Derek
Armstrong, Stuart
Stewart, James P.
Brown, Steve D. M.
Bingle, Lynne
Bingle, Colin D.
author_facet Mulay, Apoorva
Akram, Khondoker M.
Williams, Debbie
Armes, Hannah
Russell, Catherine
Hood, Derek
Armstrong, Stuart
Stewart, James P.
Brown, Steve D. M.
Bingle, Lynne
Bingle, Colin D.
author_sort Mulay, Apoorva
collection PubMed
description Otitis media (OM), or middle ear inflammation, is the most common paediatric disease and leads to significant morbidity. Although understanding of underlying disease mechanisms is hampered by complex pathophysiology it is clear that epithelial abnormalities underpin the disease. There is currently a lack of a well-characterised in vitro model of the middle ear (ME) epithelium that replicates the complex cellular composition of the middle ear. Here, we report the development of a novel in vitro model of mouse middle ear epithelial cells (mMECs) at an air–liquid interface (ALI) that recapitulates the characteristics of the native murine ME epithelium. We demonstrate that mMECs undergo differentiation into the varied cell populations seen within the native middle ear. Proteomic analysis confirmed that the cultures secrete a multitude of innate defence proteins from their apical surface. We showed that the mMECs supported the growth of the otopathogen, nontypeable Haemophilus influenzae (NTHi), suggesting that the model can be successfully utilised to study host–pathogen interactions in the middle ear. Overall, our mMEC culture system can help to better understand the cell biology of the middle ear and improve our understanding of the pathophysiology of OM. The model also has the potential to serve as a platform for validation of treatments designed to reverse aspects of epithelial remodelling that underpin OM development.
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spelling pubmed-51172332016-12-12 An in vitro model of murine middle ear epithelium Mulay, Apoorva Akram, Khondoker M. Williams, Debbie Armes, Hannah Russell, Catherine Hood, Derek Armstrong, Stuart Stewart, James P. Brown, Steve D. M. Bingle, Lynne Bingle, Colin D. Dis Model Mech Resource Article Otitis media (OM), or middle ear inflammation, is the most common paediatric disease and leads to significant morbidity. Although understanding of underlying disease mechanisms is hampered by complex pathophysiology it is clear that epithelial abnormalities underpin the disease. There is currently a lack of a well-characterised in vitro model of the middle ear (ME) epithelium that replicates the complex cellular composition of the middle ear. Here, we report the development of a novel in vitro model of mouse middle ear epithelial cells (mMECs) at an air–liquid interface (ALI) that recapitulates the characteristics of the native murine ME epithelium. We demonstrate that mMECs undergo differentiation into the varied cell populations seen within the native middle ear. Proteomic analysis confirmed that the cultures secrete a multitude of innate defence proteins from their apical surface. We showed that the mMECs supported the growth of the otopathogen, nontypeable Haemophilus influenzae (NTHi), suggesting that the model can be successfully utilised to study host–pathogen interactions in the middle ear. Overall, our mMEC culture system can help to better understand the cell biology of the middle ear and improve our understanding of the pathophysiology of OM. The model also has the potential to serve as a platform for validation of treatments designed to reverse aspects of epithelial remodelling that underpin OM development. The Company of Biologists Ltd 2016-11-01 /pmc/articles/PMC5117233/ /pubmed/27660200 http://dx.doi.org/10.1242/dmm.026658 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Resource Article
Mulay, Apoorva
Akram, Khondoker M.
Williams, Debbie
Armes, Hannah
Russell, Catherine
Hood, Derek
Armstrong, Stuart
Stewart, James P.
Brown, Steve D. M.
Bingle, Lynne
Bingle, Colin D.
An in vitro model of murine middle ear epithelium
title An in vitro model of murine middle ear epithelium
title_full An in vitro model of murine middle ear epithelium
title_fullStr An in vitro model of murine middle ear epithelium
title_full_unstemmed An in vitro model of murine middle ear epithelium
title_short An in vitro model of murine middle ear epithelium
title_sort in vitro model of murine middle ear epithelium
topic Resource Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117233/
https://www.ncbi.nlm.nih.gov/pubmed/27660200
http://dx.doi.org/10.1242/dmm.026658
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