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Non-destructive vacuum-assisted measurement of lung elastic modulus

In living tissues, mechanical stiffness and biological function are intrinsically linked. Alterations in the stiffness of tissues can induce pathological interactions that affect cellular activity and tissue function. Underlying connections between tissue stiffness and disease highlights the importa...

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Autores principales: Chen, Jiawen, Mir, Seyed Mohammad, Pinezich, Meghan R., O’Neill, John D., Guenthart, Brandon A., Bacchetta, Matthew, Vunjak-Novakovic, Gordana, Huang, Sarah X.L., Kim, Jinho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245063/
https://www.ncbi.nlm.nih.gov/pubmed/34192570
http://dx.doi.org/10.1016/j.actbio.2021.06.037
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author Chen, Jiawen
Mir, Seyed Mohammad
Pinezich, Meghan R.
O’Neill, John D.
Guenthart, Brandon A.
Bacchetta, Matthew
Vunjak-Novakovic, Gordana
Huang, Sarah X.L.
Kim, Jinho
author_facet Chen, Jiawen
Mir, Seyed Mohammad
Pinezich, Meghan R.
O’Neill, John D.
Guenthart, Brandon A.
Bacchetta, Matthew
Vunjak-Novakovic, Gordana
Huang, Sarah X.L.
Kim, Jinho
author_sort Chen, Jiawen
collection PubMed
description In living tissues, mechanical stiffness and biological function are intrinsically linked. Alterations in the stiffness of tissues can induce pathological interactions that affect cellular activity and tissue function. Underlying connections between tissue stiffness and disease highlights the importance of accurate quantitative characterizations of soft tissue mechanics, which can improve our understanding of disease and inform therapeutic development. In particular, accurate measurement of lung mechanical properties has been especially challenging due to the anatomical and mechanobiological complexities of the lung. Discrepancies between measured mechanical properties of dissected lung tissue samples and intact lung tissues in vivo has limited the ability to accurately characterize integral lung mechanics. Here, we report a non-destructive vacuum-assisted method to evaluate mechanical properties of soft biomaterials, including intact tissues and hydrogels. Using this approach, we measured elastic moduli of rat lung tissue that varied depending on stress-strain distribution throughout the lung. We also observed that the elastic moduli of enzymatically disrupted lung parenchyma increased by at least 64%. The reported methodology enables assessment of the nonlinear viscoelastic characteristics of intact lungs under normal and abnormal (i.e., injured, diseased) conditions and allows measurement of mechanical properties of tissue-mimetic biomaterials for use in therapeutics or in vitro models.
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spelling pubmed-92450632022-06-30 Non-destructive vacuum-assisted measurement of lung elastic modulus Chen, Jiawen Mir, Seyed Mohammad Pinezich, Meghan R. O’Neill, John D. Guenthart, Brandon A. Bacchetta, Matthew Vunjak-Novakovic, Gordana Huang, Sarah X.L. Kim, Jinho Acta Biomater Article In living tissues, mechanical stiffness and biological function are intrinsically linked. Alterations in the stiffness of tissues can induce pathological interactions that affect cellular activity and tissue function. Underlying connections between tissue stiffness and disease highlights the importance of accurate quantitative characterizations of soft tissue mechanics, which can improve our understanding of disease and inform therapeutic development. In particular, accurate measurement of lung mechanical properties has been especially challenging due to the anatomical and mechanobiological complexities of the lung. Discrepancies between measured mechanical properties of dissected lung tissue samples and intact lung tissues in vivo has limited the ability to accurately characterize integral lung mechanics. Here, we report a non-destructive vacuum-assisted method to evaluate mechanical properties of soft biomaterials, including intact tissues and hydrogels. Using this approach, we measured elastic moduli of rat lung tissue that varied depending on stress-strain distribution throughout the lung. We also observed that the elastic moduli of enzymatically disrupted lung parenchyma increased by at least 64%. The reported methodology enables assessment of the nonlinear viscoelastic characteristics of intact lungs under normal and abnormal (i.e., injured, diseased) conditions and allows measurement of mechanical properties of tissue-mimetic biomaterials for use in therapeutics or in vitro models. 2021-09-01 2021-06-27 /pmc/articles/PMC9245063/ /pubmed/34192570 http://dx.doi.org/10.1016/j.actbio.2021.06.037 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Article
Chen, Jiawen
Mir, Seyed Mohammad
Pinezich, Meghan R.
O’Neill, John D.
Guenthart, Brandon A.
Bacchetta, Matthew
Vunjak-Novakovic, Gordana
Huang, Sarah X.L.
Kim, Jinho
Non-destructive vacuum-assisted measurement of lung elastic modulus
title Non-destructive vacuum-assisted measurement of lung elastic modulus
title_full Non-destructive vacuum-assisted measurement of lung elastic modulus
title_fullStr Non-destructive vacuum-assisted measurement of lung elastic modulus
title_full_unstemmed Non-destructive vacuum-assisted measurement of lung elastic modulus
title_short Non-destructive vacuum-assisted measurement of lung elastic modulus
title_sort non-destructive vacuum-assisted measurement of lung elastic modulus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245063/
https://www.ncbi.nlm.nih.gov/pubmed/34192570
http://dx.doi.org/10.1016/j.actbio.2021.06.037
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