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Multiple neuron clusters on Micro-Electrode Arrays as an in vitro model of brain network
Understanding the brain functioning is essential for governing brain processes with the aim of managing pathological network dysfunctions. Due to the morphological and biochemical complexity of the central nervous system, the development of general models with predictive power must start from in vit...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511538/ https://www.ncbi.nlm.nih.gov/pubmed/37730890 http://dx.doi.org/10.1038/s41598-023-42168-0 |
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author | Brofiga, Martina Losacco, Serena Poggio, Fabio Zerbo, Roberta Arianna Milanese, Marco Massobrio, Paolo Burlando, Bruno |
author_facet | Brofiga, Martina Losacco, Serena Poggio, Fabio Zerbo, Roberta Arianna Milanese, Marco Massobrio, Paolo Burlando, Bruno |
author_sort | Brofiga, Martina |
collection | PubMed |
description | Understanding the brain functioning is essential for governing brain processes with the aim of managing pathological network dysfunctions. Due to the morphological and biochemical complexity of the central nervous system, the development of general models with predictive power must start from in vitro brain network engineering. In the present work, we realized a micro-electrode array (MEA)-based in vitro brain network and studied its emerging dynamical properties. We obtained four-neuron-clusters (4N) assemblies by plating rat embryo cortical neurons on 60-electrode MEA with cross-shaped polymeric masks and compared the emerging dynamics with those of sister single networks (1N). Both 1N and 4N assemblies exhibited spontaneous electrical activity characterized by spiking and bursting signals up to global activation by means of network bursts. Data revealed distinct patterns of network activity with differences between 1 and 4N. Rhythmic network bursts and dominant initiator clusters suggested pacemaker activities in both assembly types, but the propagation of activation sequences was statistically influenced by the assembly topology. We proved that this rhythmic activity was ivabradine sensitive, suggesting the involvement of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels, and propagated across the real clusters of 4N, or corresponding virtual clusters of 1N, with dominant initiator clusters, and nonrandom cluster activation sequences. The occurrence of nonrandom series of identical activation sequences in 4N revealed processes possibly ascribable to neuroplasticity. Hence, our multi-network dissociated cortical assemblies suggest the relevance of pacemaker neurons as essential elements for generating brain network electrophysiological patterns; indeed, such evidence should be considered in the development of computational models for envisaging network behavior both in physiological and pathological conditions. |
format | Online Article Text |
id | pubmed-10511538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105115382023-09-22 Multiple neuron clusters on Micro-Electrode Arrays as an in vitro model of brain network Brofiga, Martina Losacco, Serena Poggio, Fabio Zerbo, Roberta Arianna Milanese, Marco Massobrio, Paolo Burlando, Bruno Sci Rep Article Understanding the brain functioning is essential for governing brain processes with the aim of managing pathological network dysfunctions. Due to the morphological and biochemical complexity of the central nervous system, the development of general models with predictive power must start from in vitro brain network engineering. In the present work, we realized a micro-electrode array (MEA)-based in vitro brain network and studied its emerging dynamical properties. We obtained four-neuron-clusters (4N) assemblies by plating rat embryo cortical neurons on 60-electrode MEA with cross-shaped polymeric masks and compared the emerging dynamics with those of sister single networks (1N). Both 1N and 4N assemblies exhibited spontaneous electrical activity characterized by spiking and bursting signals up to global activation by means of network bursts. Data revealed distinct patterns of network activity with differences between 1 and 4N. Rhythmic network bursts and dominant initiator clusters suggested pacemaker activities in both assembly types, but the propagation of activation sequences was statistically influenced by the assembly topology. We proved that this rhythmic activity was ivabradine sensitive, suggesting the involvement of hyperpolarization-activated cyclic nucleotide-gated (HCN) channels, and propagated across the real clusters of 4N, or corresponding virtual clusters of 1N, with dominant initiator clusters, and nonrandom cluster activation sequences. The occurrence of nonrandom series of identical activation sequences in 4N revealed processes possibly ascribable to neuroplasticity. Hence, our multi-network dissociated cortical assemblies suggest the relevance of pacemaker neurons as essential elements for generating brain network electrophysiological patterns; indeed, such evidence should be considered in the development of computational models for envisaging network behavior both in physiological and pathological conditions. Nature Publishing Group UK 2023-09-20 /pmc/articles/PMC10511538/ /pubmed/37730890 http://dx.doi.org/10.1038/s41598-023-42168-0 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 Brofiga, Martina Losacco, Serena Poggio, Fabio Zerbo, Roberta Arianna Milanese, Marco Massobrio, Paolo Burlando, Bruno Multiple neuron clusters on Micro-Electrode Arrays as an in vitro model of brain network |
title | Multiple neuron clusters on Micro-Electrode Arrays as an in vitro model of brain network |
title_full | Multiple neuron clusters on Micro-Electrode Arrays as an in vitro model of brain network |
title_fullStr | Multiple neuron clusters on Micro-Electrode Arrays as an in vitro model of brain network |
title_full_unstemmed | Multiple neuron clusters on Micro-Electrode Arrays as an in vitro model of brain network |
title_short | Multiple neuron clusters on Micro-Electrode Arrays as an in vitro model of brain network |
title_sort | multiple neuron clusters on micro-electrode arrays as an in vitro model of brain network |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511538/ https://www.ncbi.nlm.nih.gov/pubmed/37730890 http://dx.doi.org/10.1038/s41598-023-42168-0 |
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