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Self-organization of in vitro neuronal assemblies drives to complex network topology

Activity-dependent self-organization plays an important role in the formation of specific and stereotyped connectivity patterns in neural circuits. By combining neuronal cultures, and tools with approaches from network neuroscience and information theory, we can study how complex network topology em...

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Autores principales: Antonello, Priscila C, Varley, Thomas F, Beggs, John, Porcionatto, Marimélia, Sporns, Olaf, Faber, Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203058/
https://www.ncbi.nlm.nih.gov/pubmed/35708741
http://dx.doi.org/10.7554/eLife.74921
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author Antonello, Priscila C
Varley, Thomas F
Beggs, John
Porcionatto, Marimélia
Sporns, Olaf
Faber, Jean
author_facet Antonello, Priscila C
Varley, Thomas F
Beggs, John
Porcionatto, Marimélia
Sporns, Olaf
Faber, Jean
author_sort Antonello, Priscila C
collection PubMed
description Activity-dependent self-organization plays an important role in the formation of specific and stereotyped connectivity patterns in neural circuits. By combining neuronal cultures, and tools with approaches from network neuroscience and information theory, we can study how complex network topology emerges from local neuronal interactions. We constructed effective connectivity networks using a transfer entropy analysis of spike trains recorded from rat embryo dissociated hippocampal neuron cultures between 6 and 35 days in vitro to investigate how the topology evolves during maturation. The methodology for constructing the networks considered the synapse delay and addressed the influence of firing rate and population bursts as well as spurious effects on the inference of connections. We found that the number of links in the networks grew over the course of development, shifting from a segregated to a more integrated architecture. As part of this progression, three significant aspects of complex network topology emerged. In agreement with previous in silico and in vitro studies, a small-world architecture was detected, largely due to strong clustering among neurons. Additionally, the networks developed in a modular topology, with most modules comprising nearby neurons. Finally, highly active neurons acquired topological characteristics that made them important nodes to the network and integrators of modules. These findings leverage new insights into how neuronal effective network topology relates to neuronal assembly self-organization mechanisms.
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spelling pubmed-92030582022-06-17 Self-organization of in vitro neuronal assemblies drives to complex network topology Antonello, Priscila C Varley, Thomas F Beggs, John Porcionatto, Marimélia Sporns, Olaf Faber, Jean eLife Neuroscience Activity-dependent self-organization plays an important role in the formation of specific and stereotyped connectivity patterns in neural circuits. By combining neuronal cultures, and tools with approaches from network neuroscience and information theory, we can study how complex network topology emerges from local neuronal interactions. We constructed effective connectivity networks using a transfer entropy analysis of spike trains recorded from rat embryo dissociated hippocampal neuron cultures between 6 and 35 days in vitro to investigate how the topology evolves during maturation. The methodology for constructing the networks considered the synapse delay and addressed the influence of firing rate and population bursts as well as spurious effects on the inference of connections. We found that the number of links in the networks grew over the course of development, shifting from a segregated to a more integrated architecture. As part of this progression, three significant aspects of complex network topology emerged. In agreement with previous in silico and in vitro studies, a small-world architecture was detected, largely due to strong clustering among neurons. Additionally, the networks developed in a modular topology, with most modules comprising nearby neurons. Finally, highly active neurons acquired topological characteristics that made them important nodes to the network and integrators of modules. These findings leverage new insights into how neuronal effective network topology relates to neuronal assembly self-organization mechanisms. eLife Sciences Publications, Ltd 2022-06-16 /pmc/articles/PMC9203058/ /pubmed/35708741 http://dx.doi.org/10.7554/eLife.74921 Text en © 2022, Antonello et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Antonello, Priscila C
Varley, Thomas F
Beggs, John
Porcionatto, Marimélia
Sporns, Olaf
Faber, Jean
Self-organization of in vitro neuronal assemblies drives to complex network topology
title Self-organization of in vitro neuronal assemblies drives to complex network topology
title_full Self-organization of in vitro neuronal assemblies drives to complex network topology
title_fullStr Self-organization of in vitro neuronal assemblies drives to complex network topology
title_full_unstemmed Self-organization of in vitro neuronal assemblies drives to complex network topology
title_short Self-organization of in vitro neuronal assemblies drives to complex network topology
title_sort self-organization of in vitro neuronal assemblies drives to complex network topology
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9203058/
https://www.ncbi.nlm.nih.gov/pubmed/35708741
http://dx.doi.org/10.7554/eLife.74921
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