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Live imaging of alveologenesis in precision-cut lung slices reveals dynamic epithelial cell behaviour
Damage to alveoli, the gas-exchanging region of the lungs, is a component of many chronic and acute lung diseases. In addition, insufficient generation of alveoli results in bronchopulmonary dysplasia, a disease of prematurity. Therefore visualising the process of alveolar development (alveologenesi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414680/ https://www.ncbi.nlm.nih.gov/pubmed/30862802 http://dx.doi.org/10.1038/s41467-019-09067-3 |
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author | Akram, Khondoker M. Yates, Laura L. Mongey, Róisín Rothery, Stephen Gaboriau, David C. A. Sanderson, Jeremy Hind, Matthew Griffiths, Mark Dean, Charlotte H. |
author_facet | Akram, Khondoker M. Yates, Laura L. Mongey, Róisín Rothery, Stephen Gaboriau, David C. A. Sanderson, Jeremy Hind, Matthew Griffiths, Mark Dean, Charlotte H. |
author_sort | Akram, Khondoker M. |
collection | PubMed |
description | Damage to alveoli, the gas-exchanging region of the lungs, is a component of many chronic and acute lung diseases. In addition, insufficient generation of alveoli results in bronchopulmonary dysplasia, a disease of prematurity. Therefore visualising the process of alveolar development (alveologenesis) is critical for our understanding of lung homeostasis and for the development of treatments to repair and regenerate lung tissue. Here we show live alveologenesis, using long-term, time-lapse imaging of precision-cut lung slices. We reveal that during this process, epithelial cells are highly mobile and we identify specific cell behaviours that contribute to alveologenesis: cell clustering, hollowing and cell extension. Using the cytoskeleton inhibitors blebbistatin and cytochalasin D, we show that cell migration is a key driver of alveologenesis. This study reveals important novel information about lung biology and provides a new system in which to manipulate alveologenesis genetically and pharmacologically. |
format | Online Article Text |
id | pubmed-6414680 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64146802019-03-14 Live imaging of alveologenesis in precision-cut lung slices reveals dynamic epithelial cell behaviour Akram, Khondoker M. Yates, Laura L. Mongey, Róisín Rothery, Stephen Gaboriau, David C. A. Sanderson, Jeremy Hind, Matthew Griffiths, Mark Dean, Charlotte H. Nat Commun Article Damage to alveoli, the gas-exchanging region of the lungs, is a component of many chronic and acute lung diseases. In addition, insufficient generation of alveoli results in bronchopulmonary dysplasia, a disease of prematurity. Therefore visualising the process of alveolar development (alveologenesis) is critical for our understanding of lung homeostasis and for the development of treatments to repair and regenerate lung tissue. Here we show live alveologenesis, using long-term, time-lapse imaging of precision-cut lung slices. We reveal that during this process, epithelial cells are highly mobile and we identify specific cell behaviours that contribute to alveologenesis: cell clustering, hollowing and cell extension. Using the cytoskeleton inhibitors blebbistatin and cytochalasin D, we show that cell migration is a key driver of alveologenesis. This study reveals important novel information about lung biology and provides a new system in which to manipulate alveologenesis genetically and pharmacologically. Nature Publishing Group UK 2019-03-12 /pmc/articles/PMC6414680/ /pubmed/30862802 http://dx.doi.org/10.1038/s41467-019-09067-3 Text en © The Author(s) 2019 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 Akram, Khondoker M. Yates, Laura L. Mongey, Róisín Rothery, Stephen Gaboriau, David C. A. Sanderson, Jeremy Hind, Matthew Griffiths, Mark Dean, Charlotte H. Live imaging of alveologenesis in precision-cut lung slices reveals dynamic epithelial cell behaviour |
title | Live imaging of alveologenesis in precision-cut lung slices reveals dynamic epithelial cell behaviour |
title_full | Live imaging of alveologenesis in precision-cut lung slices reveals dynamic epithelial cell behaviour |
title_fullStr | Live imaging of alveologenesis in precision-cut lung slices reveals dynamic epithelial cell behaviour |
title_full_unstemmed | Live imaging of alveologenesis in precision-cut lung slices reveals dynamic epithelial cell behaviour |
title_short | Live imaging of alveologenesis in precision-cut lung slices reveals dynamic epithelial cell behaviour |
title_sort | live imaging of alveologenesis in precision-cut lung slices reveals dynamic epithelial cell behaviour |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414680/ https://www.ncbi.nlm.nih.gov/pubmed/30862802 http://dx.doi.org/10.1038/s41467-019-09067-3 |
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