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The transcriptional landscape of the cultured murine middle ear epithelium in vitro
Otitis media (OM) 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. The mechanisms underpinning epithelial remodelli...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8084567/ https://www.ncbi.nlm.nih.gov/pubmed/33913472 http://dx.doi.org/10.1242/bio.056564 |
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author | Mulay, Apoorva Chowdhury, Md Miraj K. James, Cameron T. Bingle, Lynne Bingle, Colin D. |
author_facet | Mulay, Apoorva Chowdhury, Md Miraj K. James, Cameron T. Bingle, Lynne Bingle, Colin D. |
author_sort | Mulay, Apoorva |
collection | PubMed |
description | Otitis media (OM) 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. The mechanisms underpinning epithelial remodelling in OM remain unclear. We recently described a novel in vitro model of mouse middle ear epithelial cells (mMEECs) that undergoes mucociliary differentiation into the varied epithelial cell populations seen in the middle ear cavity. We now describe genome wide gene expression profiles of mMEECs as they undergo differentiation. We compared the gene expression profiles of original (uncultured) middle ear cells, confluent cultures of undifferentiated cells and cells that had been differentiated for 7 days at an air liquid interface (ALI). >5000 genes were differentially expressed among the three groups of cells. Approximately 4000 genes were differentially expressed between the original cells and day 0 of ALI culture. The original cell population was shown to contain a mix of cell types, including contaminating inflammatory cells that were lost on culture. Approximately 500 genes were upregulated during ALI induced differentiation. These included some secretory genes and some enzymes but most were associated with the process of ciliogenesis. The data suggest that the in vitro model of differentiated murine middle ear epithelium exhibits a transcriptional profile consistent with the mucociliary epithelium seen within the middle ear. Knowledge of the transcriptional landscape of this epithelium will provide a basis for understanding the phenotypic changes seen in murine models of OM. |
format | Online Article Text |
id | pubmed-8084567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-80845672021-04-30 The transcriptional landscape of the cultured murine middle ear epithelium in vitro Mulay, Apoorva Chowdhury, Md Miraj K. James, Cameron T. Bingle, Lynne Bingle, Colin D. Biol Open Research Article Otitis media (OM) 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. The mechanisms underpinning epithelial remodelling in OM remain unclear. We recently described a novel in vitro model of mouse middle ear epithelial cells (mMEECs) that undergoes mucociliary differentiation into the varied epithelial cell populations seen in the middle ear cavity. We now describe genome wide gene expression profiles of mMEECs as they undergo differentiation. We compared the gene expression profiles of original (uncultured) middle ear cells, confluent cultures of undifferentiated cells and cells that had been differentiated for 7 days at an air liquid interface (ALI). >5000 genes were differentially expressed among the three groups of cells. Approximately 4000 genes were differentially expressed between the original cells and day 0 of ALI culture. The original cell population was shown to contain a mix of cell types, including contaminating inflammatory cells that were lost on culture. Approximately 500 genes were upregulated during ALI induced differentiation. These included some secretory genes and some enzymes but most were associated with the process of ciliogenesis. The data suggest that the in vitro model of differentiated murine middle ear epithelium exhibits a transcriptional profile consistent with the mucociliary epithelium seen within the middle ear. Knowledge of the transcriptional landscape of this epithelium will provide a basis for understanding the phenotypic changes seen in murine models of OM. The Company of Biologists Ltd 2021-04-23 /pmc/articles/PMC8084567/ /pubmed/33913472 http://dx.doi.org/10.1242/bio.056564 Text en © 2021. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Mulay, Apoorva Chowdhury, Md Miraj K. James, Cameron T. Bingle, Lynne Bingle, Colin D. The transcriptional landscape of the cultured murine middle ear epithelium in vitro |
title | The transcriptional landscape of the cultured murine middle ear epithelium in vitro |
title_full | The transcriptional landscape of the cultured murine middle ear epithelium in vitro |
title_fullStr | The transcriptional landscape of the cultured murine middle ear epithelium in vitro |
title_full_unstemmed | The transcriptional landscape of the cultured murine middle ear epithelium in vitro |
title_short | The transcriptional landscape of the cultured murine middle ear epithelium in vitro |
title_sort | transcriptional landscape of the cultured murine middle ear epithelium in vitro |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8084567/ https://www.ncbi.nlm.nih.gov/pubmed/33913472 http://dx.doi.org/10.1242/bio.056564 |
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