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Anionic polymers amplify electrokinetic perfusion through extracellular matrices

Electrical stimulation (ES) promotes healing of chronic epidermal wounds and delays degeneration of articular cartilage. Despite electrotherapeutic treatment of these non-excitable tissues, the mechanisms by which ES promotes repair are unknown. We hypothesize that a beneficial role of ES is depende...

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Autores principales: Walker, Joseph C., Jorgensen, Ashley M., Sarkar, Anyesha, Gent, Stephen P., Messerli, Mark A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9548625/
https://www.ncbi.nlm.nih.gov/pubmed/36225599
http://dx.doi.org/10.3389/fbioe.2022.983317
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author Walker, Joseph C.
Jorgensen, Ashley M.
Sarkar, Anyesha
Gent, Stephen P.
Messerli, Mark A.
author_facet Walker, Joseph C.
Jorgensen, Ashley M.
Sarkar, Anyesha
Gent, Stephen P.
Messerli, Mark A.
author_sort Walker, Joseph C.
collection PubMed
description Electrical stimulation (ES) promotes healing of chronic epidermal wounds and delays degeneration of articular cartilage. Despite electrotherapeutic treatment of these non-excitable tissues, the mechanisms by which ES promotes repair are unknown. We hypothesize that a beneficial role of ES is dependent on electrokinetic perfusion in the extracellular space and that it mimics the effects of interstitial flow. In vivo, the extracellular space contains mixtures of extracellular proteins and negatively charged glycosaminoglycans and proteoglycans surrounding cells. While these anionic macromolecules promote water retention and increase mechanical support under compression, in the presence of ES they should also enhance electro-osmotic flow (EOF) to a greater extent than proteins alone. To test this hypothesis, we compare EOF rates between artificial matrices of gelatin (denatured collagen) with matrices of gelatin mixed with anionic polymers to mimic endogenous charged macromolecules. We report that addition of anionic polymers amplifies EOF and that a matrix comprised of 0.5% polyacrylate and 1.5% gelatin generates EOF with similar rates to those reported in cartilage. The enhanced EOF reduces mortality of cells at lower applied voltage compared to gelatin matrices alone. We also use modeling to describe the range of thermal changes that occur during these electrokinetic experiments and during electrokinetic perfusion of soft tissues. We conclude that the negative charge density of native extracellular matrices promotes electrokinetic perfusion during electrical therapies in soft tissues and may promote survival of artificial tissues and organs prior to vascularization and during transplantation.
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spelling pubmed-95486252022-10-11 Anionic polymers amplify electrokinetic perfusion through extracellular matrices Walker, Joseph C. Jorgensen, Ashley M. Sarkar, Anyesha Gent, Stephen P. Messerli, Mark A. Front Bioeng Biotechnol Bioengineering and Biotechnology Electrical stimulation (ES) promotes healing of chronic epidermal wounds and delays degeneration of articular cartilage. Despite electrotherapeutic treatment of these non-excitable tissues, the mechanisms by which ES promotes repair are unknown. We hypothesize that a beneficial role of ES is dependent on electrokinetic perfusion in the extracellular space and that it mimics the effects of interstitial flow. In vivo, the extracellular space contains mixtures of extracellular proteins and negatively charged glycosaminoglycans and proteoglycans surrounding cells. While these anionic macromolecules promote water retention and increase mechanical support under compression, in the presence of ES they should also enhance electro-osmotic flow (EOF) to a greater extent than proteins alone. To test this hypothesis, we compare EOF rates between artificial matrices of gelatin (denatured collagen) with matrices of gelatin mixed with anionic polymers to mimic endogenous charged macromolecules. We report that addition of anionic polymers amplifies EOF and that a matrix comprised of 0.5% polyacrylate and 1.5% gelatin generates EOF with similar rates to those reported in cartilage. The enhanced EOF reduces mortality of cells at lower applied voltage compared to gelatin matrices alone. We also use modeling to describe the range of thermal changes that occur during these electrokinetic experiments and during electrokinetic perfusion of soft tissues. We conclude that the negative charge density of native extracellular matrices promotes electrokinetic perfusion during electrical therapies in soft tissues and may promote survival of artificial tissues and organs prior to vascularization and during transplantation. Frontiers Media S.A. 2022-09-26 /pmc/articles/PMC9548625/ /pubmed/36225599 http://dx.doi.org/10.3389/fbioe.2022.983317 Text en Copyright © 2022 Walker, Jorgensen, Sarkar, Gent and Messerli. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Walker, Joseph C.
Jorgensen, Ashley M.
Sarkar, Anyesha
Gent, Stephen P.
Messerli, Mark A.
Anionic polymers amplify electrokinetic perfusion through extracellular matrices
title Anionic polymers amplify electrokinetic perfusion through extracellular matrices
title_full Anionic polymers amplify electrokinetic perfusion through extracellular matrices
title_fullStr Anionic polymers amplify electrokinetic perfusion through extracellular matrices
title_full_unstemmed Anionic polymers amplify electrokinetic perfusion through extracellular matrices
title_short Anionic polymers amplify electrokinetic perfusion through extracellular matrices
title_sort anionic polymers amplify electrokinetic perfusion through extracellular matrices
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9548625/
https://www.ncbi.nlm.nih.gov/pubmed/36225599
http://dx.doi.org/10.3389/fbioe.2022.983317
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