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The strain-generated electrical potential in cartilaginous tissues: a role for piezoelectricity
The strain-generated potential (SGP) is a well-established mechanism in cartilaginous tissues whereby mechanical forces generate electrical potentials. In articular cartilage (AC) and the intervertebral disc (IVD), studies on the SGP have focused on fluid- and ionic-driven effects, namely Donnan, di...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930161/ https://www.ncbi.nlm.nih.gov/pubmed/33747246 http://dx.doi.org/10.1007/s12551-021-00779-9 |
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author | Poillot, Philip Le Maitre, Christine L. Huyghe, Jacques M. |
author_facet | Poillot, Philip Le Maitre, Christine L. Huyghe, Jacques M. |
author_sort | Poillot, Philip |
collection | PubMed |
description | The strain-generated potential (SGP) is a well-established mechanism in cartilaginous tissues whereby mechanical forces generate electrical potentials. In articular cartilage (AC) and the intervertebral disc (IVD), studies on the SGP have focused on fluid- and ionic-driven effects, namely Donnan, diffusion and streaming potentials. However, recent evidence has indicated a direct coupling between strain and electrical potential. Piezoelectricity is one such mechanism whereby deformation of most biological structures, like collagen, can directly generate an electrical potential. In this review, the SGP in AC and the IVD will be revisited in light of piezoelectricity and mechanotransduction. While the evidence base for physiologically significant piezoelectric responses in tissue is lacking, difficulties in quantifying the physiological response and imperfect measurement techniques may have underestimated the property. Hindering our understanding of the SGP further, numerical models to-date have negated ferroelectric effects in the SGP and have utilised classic Donnan theory that, as evidence argues, may be oversimplified. Moreover, changes in the SGP with degeneration due to an altered extracellular matrix (ECM) indicate that the significance of ionic-driven mechanisms may diminish relative to the piezoelectric response. The SGP, and these mechanisms behind it, are finally discussed in relation to the cell response. |
format | Online Article Text |
id | pubmed-7930161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-79301612021-03-19 The strain-generated electrical potential in cartilaginous tissues: a role for piezoelectricity Poillot, Philip Le Maitre, Christine L. Huyghe, Jacques M. Biophys Rev Review The strain-generated potential (SGP) is a well-established mechanism in cartilaginous tissues whereby mechanical forces generate electrical potentials. In articular cartilage (AC) and the intervertebral disc (IVD), studies on the SGP have focused on fluid- and ionic-driven effects, namely Donnan, diffusion and streaming potentials. However, recent evidence has indicated a direct coupling between strain and electrical potential. Piezoelectricity is one such mechanism whereby deformation of most biological structures, like collagen, can directly generate an electrical potential. In this review, the SGP in AC and the IVD will be revisited in light of piezoelectricity and mechanotransduction. While the evidence base for physiologically significant piezoelectric responses in tissue is lacking, difficulties in quantifying the physiological response and imperfect measurement techniques may have underestimated the property. Hindering our understanding of the SGP further, numerical models to-date have negated ferroelectric effects in the SGP and have utilised classic Donnan theory that, as evidence argues, may be oversimplified. Moreover, changes in the SGP with degeneration due to an altered extracellular matrix (ECM) indicate that the significance of ionic-driven mechanisms may diminish relative to the piezoelectric response. The SGP, and these mechanisms behind it, are finally discussed in relation to the cell response. Springer Berlin Heidelberg 2021-02-19 /pmc/articles/PMC7930161/ /pubmed/33747246 http://dx.doi.org/10.1007/s12551-021-00779-9 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Poillot, Philip Le Maitre, Christine L. Huyghe, Jacques M. The strain-generated electrical potential in cartilaginous tissues: a role for piezoelectricity |
title | The strain-generated electrical potential in cartilaginous tissues: a role for piezoelectricity |
title_full | The strain-generated electrical potential in cartilaginous tissues: a role for piezoelectricity |
title_fullStr | The strain-generated electrical potential in cartilaginous tissues: a role for piezoelectricity |
title_full_unstemmed | The strain-generated electrical potential in cartilaginous tissues: a role for piezoelectricity |
title_short | The strain-generated electrical potential in cartilaginous tissues: a role for piezoelectricity |
title_sort | strain-generated electrical potential in cartilaginous tissues: a role for piezoelectricity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930161/ https://www.ncbi.nlm.nih.gov/pubmed/33747246 http://dx.doi.org/10.1007/s12551-021-00779-9 |
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