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Inverse poroelasticity as a fundamental mechanism in biomechanics and mechanobiology

Understanding the mechanisms of deformation of biological materials is important for improved diagnosis and therapy, fundamental investigations in mechanobiology, and applications in tissue engineering. Here we demonstrate the essential role of interstitial fluid mobility in determining the mechanic...

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Autores principales: Ehret, Alexander E., Bircher, Kevin, Stracuzzi, Alberto, Marina, Vita, Zündel, Manuel, Mazza, Edoardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714996/
https://www.ncbi.nlm.nih.gov/pubmed/29042539
http://dx.doi.org/10.1038/s41467-017-00801-3
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author Ehret, Alexander E.
Bircher, Kevin
Stracuzzi, Alberto
Marina, Vita
Zündel, Manuel
Mazza, Edoardo
author_facet Ehret, Alexander E.
Bircher, Kevin
Stracuzzi, Alberto
Marina, Vita
Zündel, Manuel
Mazza, Edoardo
author_sort Ehret, Alexander E.
collection PubMed
description Understanding the mechanisms of deformation of biological materials is important for improved diagnosis and therapy, fundamental investigations in mechanobiology, and applications in tissue engineering. Here we demonstrate the essential role of interstitial fluid mobility in determining the mechanical properties of soft tissues. Opposite to the behavior expected for a poroelastic material, the tissue volume of different collagenous membranes is observed to strongly decrease with tensile loading. Inverse poroelasticity governs monotonic and cyclic responses of soft biomembranes, and induces chemo-mechanical coupling, such that tensile forces are modulated by the chemical potential of the interstitial fluid. Correspondingly, the osmotic pressure varies with mechanical loads, thus providing an effective mechanism for mechanotransduction. Water mobility determines the tissue’s ability to adapt to deformation through compaction and dilation of the collagen fiber network. In the near field of defects this mechanism activates the reversible formation of reinforcing collagen structures which effectively avoid propagation of cracks.
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spelling pubmed-57149962017-12-06 Inverse poroelasticity as a fundamental mechanism in biomechanics and mechanobiology Ehret, Alexander E. Bircher, Kevin Stracuzzi, Alberto Marina, Vita Zündel, Manuel Mazza, Edoardo Nat Commun Article Understanding the mechanisms of deformation of biological materials is important for improved diagnosis and therapy, fundamental investigations in mechanobiology, and applications in tissue engineering. Here we demonstrate the essential role of interstitial fluid mobility in determining the mechanical properties of soft tissues. Opposite to the behavior expected for a poroelastic material, the tissue volume of different collagenous membranes is observed to strongly decrease with tensile loading. Inverse poroelasticity governs monotonic and cyclic responses of soft biomembranes, and induces chemo-mechanical coupling, such that tensile forces are modulated by the chemical potential of the interstitial fluid. Correspondingly, the osmotic pressure varies with mechanical loads, thus providing an effective mechanism for mechanotransduction. Water mobility determines the tissue’s ability to adapt to deformation through compaction and dilation of the collagen fiber network. In the near field of defects this mechanism activates the reversible formation of reinforcing collagen structures which effectively avoid propagation of cracks. Nature Publishing Group UK 2017-10-17 /pmc/articles/PMC5714996/ /pubmed/29042539 http://dx.doi.org/10.1038/s41467-017-00801-3 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
Ehret, Alexander E.
Bircher, Kevin
Stracuzzi, Alberto
Marina, Vita
Zündel, Manuel
Mazza, Edoardo
Inverse poroelasticity as a fundamental mechanism in biomechanics and mechanobiology
title Inverse poroelasticity as a fundamental mechanism in biomechanics and mechanobiology
title_full Inverse poroelasticity as a fundamental mechanism in biomechanics and mechanobiology
title_fullStr Inverse poroelasticity as a fundamental mechanism in biomechanics and mechanobiology
title_full_unstemmed Inverse poroelasticity as a fundamental mechanism in biomechanics and mechanobiology
title_short Inverse poroelasticity as a fundamental mechanism in biomechanics and mechanobiology
title_sort inverse poroelasticity as a fundamental mechanism in biomechanics and mechanobiology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714996/
https://www.ncbi.nlm.nih.gov/pubmed/29042539
http://dx.doi.org/10.1038/s41467-017-00801-3
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