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Ultrasound-mediated piezoelectric differentiation of neuron-like PC12 cells on PVDF membranes

Electrical and/or electromechanical stimulation has been shown to play a significant role in regenerating various functionalities in soft tissues, such as tendons, muscles, and nerves. In this work, we investigate the piezoelectric polymer polyvinylidene fluoride (PVDF) as a potential substrate for...

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Autores principales: Hoop, Marcus, Chen, Xiang-Zhong, Ferrari, Aldo, Mushtaq, Fajer, Ghazaryan, Gagik, Tervoort, Theo, Poulikakos, Dimos, Nelson, Bradley, Pané, Salvador
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481323/
https://www.ncbi.nlm.nih.gov/pubmed/28642614
http://dx.doi.org/10.1038/s41598-017-03992-3
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author Hoop, Marcus
Chen, Xiang-Zhong
Ferrari, Aldo
Mushtaq, Fajer
Ghazaryan, Gagik
Tervoort, Theo
Poulikakos, Dimos
Nelson, Bradley
Pané, Salvador
author_facet Hoop, Marcus
Chen, Xiang-Zhong
Ferrari, Aldo
Mushtaq, Fajer
Ghazaryan, Gagik
Tervoort, Theo
Poulikakos, Dimos
Nelson, Bradley
Pané, Salvador
author_sort Hoop, Marcus
collection PubMed
description Electrical and/or electromechanical stimulation has been shown to play a significant role in regenerating various functionalities in soft tissues, such as tendons, muscles, and nerves. In this work, we investigate the piezoelectric polymer polyvinylidene fluoride (PVDF) as a potential substrate for wireless neuronal differentiation. Piezoelectric PVDF enables generation of electrical charges on its surface upon acoustic stimulation, inducing neuritogenesis of PC12 cells. We demonstrate that the effect of pure piezoelectric stimulation on neurite generation in PC12 cells is comparable to the ones induced by neuronal growth factor (NGF). In inhibitor experiments, our results indicate that dynamic stimulation of PVDF by ultrasonic (US) waves activates calcium channels, thus inducing the generation of neurites via a cyclic adenosine monophosphate (cAMP)-dependent pathway. This mechanism is independent from the well-studied NGF induced mitogen-activated protein kinases/extracellular signal-regulated kinases (MAPK/ERK) pathway. The use of US, in combination with piezoelectric polymers, is advantageous since focused power transmission can occur deep into biological tissues, which holds great promise for the development of non-invasive neuroregenerative devices.
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spelling pubmed-54813232017-06-26 Ultrasound-mediated piezoelectric differentiation of neuron-like PC12 cells on PVDF membranes Hoop, Marcus Chen, Xiang-Zhong Ferrari, Aldo Mushtaq, Fajer Ghazaryan, Gagik Tervoort, Theo Poulikakos, Dimos Nelson, Bradley Pané, Salvador Sci Rep Article Electrical and/or electromechanical stimulation has been shown to play a significant role in regenerating various functionalities in soft tissues, such as tendons, muscles, and nerves. In this work, we investigate the piezoelectric polymer polyvinylidene fluoride (PVDF) as a potential substrate for wireless neuronal differentiation. Piezoelectric PVDF enables generation of electrical charges on its surface upon acoustic stimulation, inducing neuritogenesis of PC12 cells. We demonstrate that the effect of pure piezoelectric stimulation on neurite generation in PC12 cells is comparable to the ones induced by neuronal growth factor (NGF). In inhibitor experiments, our results indicate that dynamic stimulation of PVDF by ultrasonic (US) waves activates calcium channels, thus inducing the generation of neurites via a cyclic adenosine monophosphate (cAMP)-dependent pathway. This mechanism is independent from the well-studied NGF induced mitogen-activated protein kinases/extracellular signal-regulated kinases (MAPK/ERK) pathway. The use of US, in combination with piezoelectric polymers, is advantageous since focused power transmission can occur deep into biological tissues, which holds great promise for the development of non-invasive neuroregenerative devices. Nature Publishing Group UK 2017-06-22 /pmc/articles/PMC5481323/ /pubmed/28642614 http://dx.doi.org/10.1038/s41598-017-03992-3 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
Hoop, Marcus
Chen, Xiang-Zhong
Ferrari, Aldo
Mushtaq, Fajer
Ghazaryan, Gagik
Tervoort, Theo
Poulikakos, Dimos
Nelson, Bradley
Pané, Salvador
Ultrasound-mediated piezoelectric differentiation of neuron-like PC12 cells on PVDF membranes
title Ultrasound-mediated piezoelectric differentiation of neuron-like PC12 cells on PVDF membranes
title_full Ultrasound-mediated piezoelectric differentiation of neuron-like PC12 cells on PVDF membranes
title_fullStr Ultrasound-mediated piezoelectric differentiation of neuron-like PC12 cells on PVDF membranes
title_full_unstemmed Ultrasound-mediated piezoelectric differentiation of neuron-like PC12 cells on PVDF membranes
title_short Ultrasound-mediated piezoelectric differentiation of neuron-like PC12 cells on PVDF membranes
title_sort ultrasound-mediated piezoelectric differentiation of neuron-like pc12 cells on pvdf membranes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481323/
https://www.ncbi.nlm.nih.gov/pubmed/28642614
http://dx.doi.org/10.1038/s41598-017-03992-3
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