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PEDOT:PSS Interfaces Support the Development of Neuronal Synaptic Networks with Reduced Neuroglia Response In vitro

The design of electrodes based on conductive polymers in brain-machine interface technology offers the opportunity to exploit variably manufactured materials to reduce gliosis, indeed the most common brain response to chronically implanted neural electrodes. In fact, the use of conductive polymers,...

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Autores principales: Cellot, Giada, Lagonegro, Paola, Tarabella, Giuseppe, Scaini, Denis, Fabbri, Filippo, Iannotta, Salvatore, Prato, Maurizio, Salviati, Giancarlo, Ballerini, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712304/
https://www.ncbi.nlm.nih.gov/pubmed/26834546
http://dx.doi.org/10.3389/fnins.2015.00521
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author Cellot, Giada
Lagonegro, Paola
Tarabella, Giuseppe
Scaini, Denis
Fabbri, Filippo
Iannotta, Salvatore
Prato, Maurizio
Salviati, Giancarlo
Ballerini, Laura
author_facet Cellot, Giada
Lagonegro, Paola
Tarabella, Giuseppe
Scaini, Denis
Fabbri, Filippo
Iannotta, Salvatore
Prato, Maurizio
Salviati, Giancarlo
Ballerini, Laura
author_sort Cellot, Giada
collection PubMed
description The design of electrodes based on conductive polymers in brain-machine interface technology offers the opportunity to exploit variably manufactured materials to reduce gliosis, indeed the most common brain response to chronically implanted neural electrodes. In fact, the use of conductive polymers, finely tailored in their physical-chemical properties, might result in electrodes with improved adaptability to the brain tissue and increased charge-transfer efficiency. Here we interfaced poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) doped with different amounts of ethylene glycol (EG) with rat hippocampal primary cultures grown for 3 weeks on these synthetic substrates. We used immunofluorescence and scanning electron microscopy (SEM) combined to single cell electrophysiology to assess the biocompatibility of PEDOT:PSS in terms of neuronal growth and synapse formation. We investigated neuronal morphology, density and electrical activity. We reported the novel observation that opposite to neurons, glial cell density was progressively reduced, hinting at the ability of this material to down regulate glial reaction. Thus, PEDOT:PSS is an attractive candidate for the design of new implantable electrodes, controlling the extent of glial reactivity without affecting neuronal viability and function.
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spelling pubmed-47123042016-01-29 PEDOT:PSS Interfaces Support the Development of Neuronal Synaptic Networks with Reduced Neuroglia Response In vitro Cellot, Giada Lagonegro, Paola Tarabella, Giuseppe Scaini, Denis Fabbri, Filippo Iannotta, Salvatore Prato, Maurizio Salviati, Giancarlo Ballerini, Laura Front Neurosci Neuroscience The design of electrodes based on conductive polymers in brain-machine interface technology offers the opportunity to exploit variably manufactured materials to reduce gliosis, indeed the most common brain response to chronically implanted neural electrodes. In fact, the use of conductive polymers, finely tailored in their physical-chemical properties, might result in electrodes with improved adaptability to the brain tissue and increased charge-transfer efficiency. Here we interfaced poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) doped with different amounts of ethylene glycol (EG) with rat hippocampal primary cultures grown for 3 weeks on these synthetic substrates. We used immunofluorescence and scanning electron microscopy (SEM) combined to single cell electrophysiology to assess the biocompatibility of PEDOT:PSS in terms of neuronal growth and synapse formation. We investigated neuronal morphology, density and electrical activity. We reported the novel observation that opposite to neurons, glial cell density was progressively reduced, hinting at the ability of this material to down regulate glial reaction. Thus, PEDOT:PSS is an attractive candidate for the design of new implantable electrodes, controlling the extent of glial reactivity without affecting neuronal viability and function. Frontiers Media S.A. 2016-01-14 /pmc/articles/PMC4712304/ /pubmed/26834546 http://dx.doi.org/10.3389/fnins.2015.00521 Text en Copyright © 2016 Cellot, Lagonegro, Tarabella, Scaini, Fabbri, Iannotta, Prato, Salviati and Ballerini. http://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) or licensor 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 Neuroscience
Cellot, Giada
Lagonegro, Paola
Tarabella, Giuseppe
Scaini, Denis
Fabbri, Filippo
Iannotta, Salvatore
Prato, Maurizio
Salviati, Giancarlo
Ballerini, Laura
PEDOT:PSS Interfaces Support the Development of Neuronal Synaptic Networks with Reduced Neuroglia Response In vitro
title PEDOT:PSS Interfaces Support the Development of Neuronal Synaptic Networks with Reduced Neuroglia Response In vitro
title_full PEDOT:PSS Interfaces Support the Development of Neuronal Synaptic Networks with Reduced Neuroglia Response In vitro
title_fullStr PEDOT:PSS Interfaces Support the Development of Neuronal Synaptic Networks with Reduced Neuroglia Response In vitro
title_full_unstemmed PEDOT:PSS Interfaces Support the Development of Neuronal Synaptic Networks with Reduced Neuroglia Response In vitro
title_short PEDOT:PSS Interfaces Support the Development of Neuronal Synaptic Networks with Reduced Neuroglia Response In vitro
title_sort pedot:pss interfaces support the development of neuronal synaptic networks with reduced neuroglia response in vitro
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712304/
https://www.ncbi.nlm.nih.gov/pubmed/26834546
http://dx.doi.org/10.3389/fnins.2015.00521
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