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Mediation of cellular osteogenic differentiation through daily stimulation time based on polypyrrole planar electrodes
In electrical stimulation (ES), daily stimulation time means the interacting duration with cells per day, and is a vital factor for mediating cellular function. In the present study, the effect of stimulation time on osteogenic differentiation of MC3T3-E1 cells was investigated under ES on polypyrro...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738366/ https://www.ncbi.nlm.nih.gov/pubmed/29263335 http://dx.doi.org/10.1038/s41598-017-17120-8 |
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author | Liu, Zongguang Dong, Lingqing Wang, Liming Wang, Xiaozhao Cheng, Kui Luo, Zhongkuan Weng, Wenjian |
author_facet | Liu, Zongguang Dong, Lingqing Wang, Liming Wang, Xiaozhao Cheng, Kui Luo, Zhongkuan Weng, Wenjian |
author_sort | Liu, Zongguang |
collection | PubMed |
description | In electrical stimulation (ES), daily stimulation time means the interacting duration with cells per day, and is a vital factor for mediating cellular function. In the present study, the effect of stimulation time on osteogenic differentiation of MC3T3-E1 cells was investigated under ES on polypyrrole (Ppy) planar interdigitated electrodes (IDE). The results demonstrated that only a suitable daily stimulation time supported to obviously upregulate the expression of ALP protein and osteogenesis-related genes (ALP, Col-I, Runx2 and OCN), while a short or long daily stimulation time showed no significant outcomes. These might be attributed to the mechanism that an ES induced transient change in intracellular calcium ion concentration, which was responsible for activating calcium ion signaling pathway to enhance cellular osteogenic differentiation. A shorter daily time could lead to insufficient duration for the transient change in intracellular calcium ion concentration, and a longer daily time could give rise to cellular fatigue with no transient change. This work therefore provides new insights into the fundamental understanding of cell responses to ES and will have an impact on further designing materials to mediate cell behaviors. |
format | Online Article Text |
id | pubmed-5738366 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57383662017-12-22 Mediation of cellular osteogenic differentiation through daily stimulation time based on polypyrrole planar electrodes Liu, Zongguang Dong, Lingqing Wang, Liming Wang, Xiaozhao Cheng, Kui Luo, Zhongkuan Weng, Wenjian Sci Rep Article In electrical stimulation (ES), daily stimulation time means the interacting duration with cells per day, and is a vital factor for mediating cellular function. In the present study, the effect of stimulation time on osteogenic differentiation of MC3T3-E1 cells was investigated under ES on polypyrrole (Ppy) planar interdigitated electrodes (IDE). The results demonstrated that only a suitable daily stimulation time supported to obviously upregulate the expression of ALP protein and osteogenesis-related genes (ALP, Col-I, Runx2 and OCN), while a short or long daily stimulation time showed no significant outcomes. These might be attributed to the mechanism that an ES induced transient change in intracellular calcium ion concentration, which was responsible for activating calcium ion signaling pathway to enhance cellular osteogenic differentiation. A shorter daily time could lead to insufficient duration for the transient change in intracellular calcium ion concentration, and a longer daily time could give rise to cellular fatigue with no transient change. This work therefore provides new insights into the fundamental understanding of cell responses to ES and will have an impact on further designing materials to mediate cell behaviors. Nature Publishing Group UK 2017-12-20 /pmc/articles/PMC5738366/ /pubmed/29263335 http://dx.doi.org/10.1038/s41598-017-17120-8 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Liu, Zongguang Dong, Lingqing Wang, Liming Wang, Xiaozhao Cheng, Kui Luo, Zhongkuan Weng, Wenjian Mediation of cellular osteogenic differentiation through daily stimulation time based on polypyrrole planar electrodes |
title | Mediation of cellular osteogenic differentiation through daily stimulation time based on polypyrrole planar electrodes |
title_full | Mediation of cellular osteogenic differentiation through daily stimulation time based on polypyrrole planar electrodes |
title_fullStr | Mediation of cellular osteogenic differentiation through daily stimulation time based on polypyrrole planar electrodes |
title_full_unstemmed | Mediation of cellular osteogenic differentiation through daily stimulation time based on polypyrrole planar electrodes |
title_short | Mediation of cellular osteogenic differentiation through daily stimulation time based on polypyrrole planar electrodes |
title_sort | mediation of cellular osteogenic differentiation through daily stimulation time based on polypyrrole planar electrodes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738366/ https://www.ncbi.nlm.nih.gov/pubmed/29263335 http://dx.doi.org/10.1038/s41598-017-17120-8 |
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