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Revealing Low Amplitude Signals of Neuroendocrine Cells through Disordered Silicon Nanowires‐Based Microelectrode Array

Today, the key methodology to study in vitro or in vivo electrical activity in a population of electrogenic cells, under physiological or pathological conditions, is by using microelectrode array (MEA). While significant efforts have been devoted to develop nanostructured MEAs for improving the elec...

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Autores principales: Maita, Francesco, Maiolo, Luca, Lucarini, Ivano, Del Rio De Vicente, Josè Ignacio, Sciortino, Antonio, Ledda, Mario, Mussi, Valentina, Lisi, Antonella, Convertino, Annalisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460871/
https://www.ncbi.nlm.nih.gov/pubmed/37357140
http://dx.doi.org/10.1002/advs.202301925
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author Maita, Francesco
Maiolo, Luca
Lucarini, Ivano
Del Rio De Vicente, Josè Ignacio
Sciortino, Antonio
Ledda, Mario
Mussi, Valentina
Lisi, Antonella
Convertino, Annalisa
author_facet Maita, Francesco
Maiolo, Luca
Lucarini, Ivano
Del Rio De Vicente, Josè Ignacio
Sciortino, Antonio
Ledda, Mario
Mussi, Valentina
Lisi, Antonella
Convertino, Annalisa
author_sort Maita, Francesco
collection PubMed
description Today, the key methodology to study in vitro or in vivo electrical activity in a population of electrogenic cells, under physiological or pathological conditions, is by using microelectrode array (MEA). While significant efforts have been devoted to develop nanostructured MEAs for improving the electrophysiological investigation in neurons and cardiomyocytes, data on the recording of the electrical activity from neuroendocrine cells with MEA technology are scarce owing to their weaker electrical signals. Disordered silicon nanowires (SiNWs) for developing a MEA that, combined with a customized acquisition board, successfully capture the electrical signals generated by the corticotrope AtT‐20 cells as a function of the extracellular calcium (Ca(2+)) concentration are reported. The recorded signals show a shape that clearly resembles the action potential waveform by suggesting a natural membrane penetration of the SiNWs. Additionally, the generation of synchronous signals observed under high Ca(2+) content indicates the occurrence of a collective behavior in the AtT‐20 cell population. This study extends the usefulness of MEA technology to the investigation of the electrical communication in cells of the pituitary gland, crucial in controlling several essential human functions, and provides new perspectives in recording with MEA the electrical activity of excitable cells.
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spelling pubmed-104608712023-08-29 Revealing Low Amplitude Signals of Neuroendocrine Cells through Disordered Silicon Nanowires‐Based Microelectrode Array Maita, Francesco Maiolo, Luca Lucarini, Ivano Del Rio De Vicente, Josè Ignacio Sciortino, Antonio Ledda, Mario Mussi, Valentina Lisi, Antonella Convertino, Annalisa Adv Sci (Weinh) Research Articles Today, the key methodology to study in vitro or in vivo electrical activity in a population of electrogenic cells, under physiological or pathological conditions, is by using microelectrode array (MEA). While significant efforts have been devoted to develop nanostructured MEAs for improving the electrophysiological investigation in neurons and cardiomyocytes, data on the recording of the electrical activity from neuroendocrine cells with MEA technology are scarce owing to their weaker electrical signals. Disordered silicon nanowires (SiNWs) for developing a MEA that, combined with a customized acquisition board, successfully capture the electrical signals generated by the corticotrope AtT‐20 cells as a function of the extracellular calcium (Ca(2+)) concentration are reported. The recorded signals show a shape that clearly resembles the action potential waveform by suggesting a natural membrane penetration of the SiNWs. Additionally, the generation of synchronous signals observed under high Ca(2+) content indicates the occurrence of a collective behavior in the AtT‐20 cell population. This study extends the usefulness of MEA technology to the investigation of the electrical communication in cells of the pituitary gland, crucial in controlling several essential human functions, and provides new perspectives in recording with MEA the electrical activity of excitable cells. John Wiley and Sons Inc. 2023-06-25 /pmc/articles/PMC10460871/ /pubmed/37357140 http://dx.doi.org/10.1002/advs.202301925 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Maita, Francesco
Maiolo, Luca
Lucarini, Ivano
Del Rio De Vicente, Josè Ignacio
Sciortino, Antonio
Ledda, Mario
Mussi, Valentina
Lisi, Antonella
Convertino, Annalisa
Revealing Low Amplitude Signals of Neuroendocrine Cells through Disordered Silicon Nanowires‐Based Microelectrode Array
title Revealing Low Amplitude Signals of Neuroendocrine Cells through Disordered Silicon Nanowires‐Based Microelectrode Array
title_full Revealing Low Amplitude Signals of Neuroendocrine Cells through Disordered Silicon Nanowires‐Based Microelectrode Array
title_fullStr Revealing Low Amplitude Signals of Neuroendocrine Cells through Disordered Silicon Nanowires‐Based Microelectrode Array
title_full_unstemmed Revealing Low Amplitude Signals of Neuroendocrine Cells through Disordered Silicon Nanowires‐Based Microelectrode Array
title_short Revealing Low Amplitude Signals of Neuroendocrine Cells through Disordered Silicon Nanowires‐Based Microelectrode Array
title_sort revealing low amplitude signals of neuroendocrine cells through disordered silicon nanowires‐based microelectrode array
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460871/
https://www.ncbi.nlm.nih.gov/pubmed/37357140
http://dx.doi.org/10.1002/advs.202301925
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