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Cell-cell interactions and fluctuations in the direction of motility promote directed migration of osteoblasts in direct current electrotaxis

Under both physiological (development, regeneration) and pathological conditions (cancer metastasis), cells migrate while sensing environmental cues in the form of mechanical, chemical or electrical stimuli. In the case of bone tissue, osteoblast migration is essential in bone regeneration. Although...

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Autores principales: Dawson, Jonathan Edward, Sellmann, Tina, Porath, Katrin, Bader, Rainer, van Rienen, Ursula, Appali, Revathi, Köhling, Rüdiger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582662/
https://www.ncbi.nlm.nih.gov/pubmed/36277406
http://dx.doi.org/10.3389/fbioe.2022.995326
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author Dawson, Jonathan Edward
Sellmann, Tina
Porath, Katrin
Bader, Rainer
van Rienen, Ursula
Appali, Revathi
Köhling, Rüdiger
author_facet Dawson, Jonathan Edward
Sellmann, Tina
Porath, Katrin
Bader, Rainer
van Rienen, Ursula
Appali, Revathi
Köhling, Rüdiger
author_sort Dawson, Jonathan Edward
collection PubMed
description Under both physiological (development, regeneration) and pathological conditions (cancer metastasis), cells migrate while sensing environmental cues in the form of mechanical, chemical or electrical stimuli. In the case of bone tissue, osteoblast migration is essential in bone regeneration. Although it is known that osteoblasts respond to exogenous electric fields, the underlying mechanism of electrotactic collective movement of human osteoblasts is unclear. Here, we present a computational model that describes the osteoblast cell migration in a direct current electric field as the motion of a collection of active self-propelled particles and takes into account fluctuations in the direction of single-cell migration, finite-range cell-cell interactions, and the interaction of a cell with the external electric field. By comparing this model with in vitro experiments in which human primary osteoblasts are exposed to a direct current electric field of different field strengths, we show that cell-cell interactions and fluctuations in the migration direction promote anode-directed collective migration of osteoblasts.
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spelling pubmed-95826622022-10-21 Cell-cell interactions and fluctuations in the direction of motility promote directed migration of osteoblasts in direct current electrotaxis Dawson, Jonathan Edward Sellmann, Tina Porath, Katrin Bader, Rainer van Rienen, Ursula Appali, Revathi Köhling, Rüdiger Front Bioeng Biotechnol Bioengineering and Biotechnology Under both physiological (development, regeneration) and pathological conditions (cancer metastasis), cells migrate while sensing environmental cues in the form of mechanical, chemical or electrical stimuli. In the case of bone tissue, osteoblast migration is essential in bone regeneration. Although it is known that osteoblasts respond to exogenous electric fields, the underlying mechanism of electrotactic collective movement of human osteoblasts is unclear. Here, we present a computational model that describes the osteoblast cell migration in a direct current electric field as the motion of a collection of active self-propelled particles and takes into account fluctuations in the direction of single-cell migration, finite-range cell-cell interactions, and the interaction of a cell with the external electric field. By comparing this model with in vitro experiments in which human primary osteoblasts are exposed to a direct current electric field of different field strengths, we show that cell-cell interactions and fluctuations in the migration direction promote anode-directed collective migration of osteoblasts. Frontiers Media S.A. 2022-10-06 /pmc/articles/PMC9582662/ /pubmed/36277406 http://dx.doi.org/10.3389/fbioe.2022.995326 Text en Copyright © 2022 Dawson, Sellmann, Porath, Bader, van Rienen, Appali and Köhling. 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
Dawson, Jonathan Edward
Sellmann, Tina
Porath, Katrin
Bader, Rainer
van Rienen, Ursula
Appali, Revathi
Köhling, Rüdiger
Cell-cell interactions and fluctuations in the direction of motility promote directed migration of osteoblasts in direct current electrotaxis
title Cell-cell interactions and fluctuations in the direction of motility promote directed migration of osteoblasts in direct current electrotaxis
title_full Cell-cell interactions and fluctuations in the direction of motility promote directed migration of osteoblasts in direct current electrotaxis
title_fullStr Cell-cell interactions and fluctuations in the direction of motility promote directed migration of osteoblasts in direct current electrotaxis
title_full_unstemmed Cell-cell interactions and fluctuations in the direction of motility promote directed migration of osteoblasts in direct current electrotaxis
title_short Cell-cell interactions and fluctuations in the direction of motility promote directed migration of osteoblasts in direct current electrotaxis
title_sort cell-cell interactions and fluctuations in the direction of motility promote directed migration of osteoblasts in direct current electrotaxis
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582662/
https://www.ncbi.nlm.nih.gov/pubmed/36277406
http://dx.doi.org/10.3389/fbioe.2022.995326
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