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Optical coherence tomography-based contact indentation for diaphragm mechanics in a mouse model of transforming growth factor alpha induced lung disease

This study tested the utility of optical coherence tomography (OCT)-based indentation to assess mechanical properties of respiratory tissues in disease. Using OCT-based indentation, the elastic modulus of mouse diaphragm was measured from changes in diaphragm thickness in response to an applied forc...

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Autores principales: Wang, Kimberley C. W., Astell, Chrissie J., Wijesinghe, Philip, Larcombe, Alexander N., Pinniger, Gavin J., Zosky, Graeme R., Kennedy, Brendan F., Berry, Luke J., Sampson, David D., James, Alan L., Le Cras, Timothy D., Noble, Peter B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431417/
https://www.ncbi.nlm.nih.gov/pubmed/28473708
http://dx.doi.org/10.1038/s41598-017-01431-x
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author Wang, Kimberley C. W.
Astell, Chrissie J.
Wijesinghe, Philip
Larcombe, Alexander N.
Pinniger, Gavin J.
Zosky, Graeme R.
Kennedy, Brendan F.
Berry, Luke J.
Sampson, David D.
James, Alan L.
Le Cras, Timothy D.
Noble, Peter B.
author_facet Wang, Kimberley C. W.
Astell, Chrissie J.
Wijesinghe, Philip
Larcombe, Alexander N.
Pinniger, Gavin J.
Zosky, Graeme R.
Kennedy, Brendan F.
Berry, Luke J.
Sampson, David D.
James, Alan L.
Le Cras, Timothy D.
Noble, Peter B.
author_sort Wang, Kimberley C. W.
collection PubMed
description This study tested the utility of optical coherence tomography (OCT)-based indentation to assess mechanical properties of respiratory tissues in disease. Using OCT-based indentation, the elastic modulus of mouse diaphragm was measured from changes in diaphragm thickness in response to an applied force provided by an indenter. We used a transgenic mouse model of chronic lung disease induced by the overexpression of transforming growth factor-alpha (TGF-α), established by the presence of pleural and peribronchial fibrosis and impaired lung mechanics determined by the forced oscillation technique and plethysmography. Diaphragm elastic modulus assessed by OCT-based indentation was reduced by TGF-α at both left and right lateral locations (p < 0.05). Diaphragm elastic modulus at left and right lateral locations were correlated within mice (r = 0.67, p < 0.01) suggesting that measurements were representative of tissue beyond the indenter field. Co-localised images of diaphragm after TGF-α overexpression revealed a layered fibrotic appearance. Maximum diaphragm force in conventional organ bath studies was also reduced by TGF-α overexpression (p < 0.01). Results show that OCT-based indentation provided clear delineation of diseased diaphragm, and together with organ bath assessment, provides new evidence suggesting that TGF-α overexpression produces impairment in diaphragm function and, therefore, an increase in the work of breathing in chronic lung disease.
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spelling pubmed-54314172017-05-16 Optical coherence tomography-based contact indentation for diaphragm mechanics in a mouse model of transforming growth factor alpha induced lung disease Wang, Kimberley C. W. Astell, Chrissie J. Wijesinghe, Philip Larcombe, Alexander N. Pinniger, Gavin J. Zosky, Graeme R. Kennedy, Brendan F. Berry, Luke J. Sampson, David D. James, Alan L. Le Cras, Timothy D. Noble, Peter B. Sci Rep Article This study tested the utility of optical coherence tomography (OCT)-based indentation to assess mechanical properties of respiratory tissues in disease. Using OCT-based indentation, the elastic modulus of mouse diaphragm was measured from changes in diaphragm thickness in response to an applied force provided by an indenter. We used a transgenic mouse model of chronic lung disease induced by the overexpression of transforming growth factor-alpha (TGF-α), established by the presence of pleural and peribronchial fibrosis and impaired lung mechanics determined by the forced oscillation technique and plethysmography. Diaphragm elastic modulus assessed by OCT-based indentation was reduced by TGF-α at both left and right lateral locations (p < 0.05). Diaphragm elastic modulus at left and right lateral locations were correlated within mice (r = 0.67, p < 0.01) suggesting that measurements were representative of tissue beyond the indenter field. Co-localised images of diaphragm after TGF-α overexpression revealed a layered fibrotic appearance. Maximum diaphragm force in conventional organ bath studies was also reduced by TGF-α overexpression (p < 0.01). Results show that OCT-based indentation provided clear delineation of diseased diaphragm, and together with organ bath assessment, provides new evidence suggesting that TGF-α overexpression produces impairment in diaphragm function and, therefore, an increase in the work of breathing in chronic lung disease. Nature Publishing Group UK 2017-05-04 /pmc/articles/PMC5431417/ /pubmed/28473708 http://dx.doi.org/10.1038/s41598-017-01431-x Text en © The Author(s) 2017 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
Wang, Kimberley C. W.
Astell, Chrissie J.
Wijesinghe, Philip
Larcombe, Alexander N.
Pinniger, Gavin J.
Zosky, Graeme R.
Kennedy, Brendan F.
Berry, Luke J.
Sampson, David D.
James, Alan L.
Le Cras, Timothy D.
Noble, Peter B.
Optical coherence tomography-based contact indentation for diaphragm mechanics in a mouse model of transforming growth factor alpha induced lung disease
title Optical coherence tomography-based contact indentation for diaphragm mechanics in a mouse model of transforming growth factor alpha induced lung disease
title_full Optical coherence tomography-based contact indentation for diaphragm mechanics in a mouse model of transforming growth factor alpha induced lung disease
title_fullStr Optical coherence tomography-based contact indentation for diaphragm mechanics in a mouse model of transforming growth factor alpha induced lung disease
title_full_unstemmed Optical coherence tomography-based contact indentation for diaphragm mechanics in a mouse model of transforming growth factor alpha induced lung disease
title_short Optical coherence tomography-based contact indentation for diaphragm mechanics in a mouse model of transforming growth factor alpha induced lung disease
title_sort optical coherence tomography-based contact indentation for diaphragm mechanics in a mouse model of transforming growth factor alpha induced lung disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5431417/
https://www.ncbi.nlm.nih.gov/pubmed/28473708
http://dx.doi.org/10.1038/s41598-017-01431-x
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