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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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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. |
format | Online Article Text |
id | pubmed-9582662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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