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Electrotaxis evokes directional separation of co-cultured keratinocytes and fibroblasts

Bioelectric communication plays a significant role in several cellular processes and biological mechanisms, such as division, differentiation, migration, cancer metastasis, and wound healing. Ion flow across cellular walls leads to potential gradients and subsequent formation of constant or time-var...

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Autores principales: Leal, José, Shaner, Sebastian, Jedrusik, Nicole, Savelyeva, Anna, Asplund, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349865/
https://www.ncbi.nlm.nih.gov/pubmed/37454232
http://dx.doi.org/10.1038/s41598-023-38664-y
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author Leal, José
Shaner, Sebastian
Jedrusik, Nicole
Savelyeva, Anna
Asplund, Maria
author_facet Leal, José
Shaner, Sebastian
Jedrusik, Nicole
Savelyeva, Anna
Asplund, Maria
author_sort Leal, José
collection PubMed
description Bioelectric communication plays a significant role in several cellular processes and biological mechanisms, such as division, differentiation, migration, cancer metastasis, and wound healing. Ion flow across cellular walls leads to potential gradients and subsequent formation of constant or time-varying electric fields(EFs), which regulate cellular processes. An EF is natively generated towards the wound center during epithelial wound healing, aiming to align and guide cell migration, particularly of macrophages, fibroblasts, and keratinocytes. While this phenomenon, known as electrotaxis or galvanotaxis, has been extensively investigated across many cell types, it is typically explored one cell type at a time, which does not accurately represent cellular interactions during complex biological processes. Here we show the co-cultured electrotaxis of epidermal keratinocytes and dermal fibroblasts with a salt-bridgeless microfluidic approach for the first time. The electrotactic response of these cells was first assessed in mono-culture to establish a baseline, resulting in the characteristic cathodic migration for keratinocytes and anodic for fibroblasts. Both cell types retained their electrotactic properties in co-culture leading to clear cellular partition even in the presence of cellular collisions. The methods leveraged here pave the way for future co-culture electrotaxis experiments where the concurrent influence of cell types can be thoroughly investigated.
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spelling pubmed-103498652023-07-17 Electrotaxis evokes directional separation of co-cultured keratinocytes and fibroblasts Leal, José Shaner, Sebastian Jedrusik, Nicole Savelyeva, Anna Asplund, Maria Sci Rep Article Bioelectric communication plays a significant role in several cellular processes and biological mechanisms, such as division, differentiation, migration, cancer metastasis, and wound healing. Ion flow across cellular walls leads to potential gradients and subsequent formation of constant or time-varying electric fields(EFs), which regulate cellular processes. An EF is natively generated towards the wound center during epithelial wound healing, aiming to align and guide cell migration, particularly of macrophages, fibroblasts, and keratinocytes. While this phenomenon, known as electrotaxis or galvanotaxis, has been extensively investigated across many cell types, it is typically explored one cell type at a time, which does not accurately represent cellular interactions during complex biological processes. Here we show the co-cultured electrotaxis of epidermal keratinocytes and dermal fibroblasts with a salt-bridgeless microfluidic approach for the first time. The electrotactic response of these cells was first assessed in mono-culture to establish a baseline, resulting in the characteristic cathodic migration for keratinocytes and anodic for fibroblasts. Both cell types retained their electrotactic properties in co-culture leading to clear cellular partition even in the presence of cellular collisions. The methods leveraged here pave the way for future co-culture electrotaxis experiments where the concurrent influence of cell types can be thoroughly investigated. Nature Publishing Group UK 2023-07-15 /pmc/articles/PMC10349865/ /pubmed/37454232 http://dx.doi.org/10.1038/s41598-023-38664-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Leal, José
Shaner, Sebastian
Jedrusik, Nicole
Savelyeva, Anna
Asplund, Maria
Electrotaxis evokes directional separation of co-cultured keratinocytes and fibroblasts
title Electrotaxis evokes directional separation of co-cultured keratinocytes and fibroblasts
title_full Electrotaxis evokes directional separation of co-cultured keratinocytes and fibroblasts
title_fullStr Electrotaxis evokes directional separation of co-cultured keratinocytes and fibroblasts
title_full_unstemmed Electrotaxis evokes directional separation of co-cultured keratinocytes and fibroblasts
title_short Electrotaxis evokes directional separation of co-cultured keratinocytes and fibroblasts
title_sort electrotaxis evokes directional separation of co-cultured keratinocytes and fibroblasts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349865/
https://www.ncbi.nlm.nih.gov/pubmed/37454232
http://dx.doi.org/10.1038/s41598-023-38664-y
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