Cargando…

Bidirectional Coupling between Astrocytes and Neurons Mediates Learning and Dynamic Coordination in the Brain: A Multiple Modeling Approach

In recent years research suggests that astrocyte networks, in addition to nutrient and waste processing functions, regulate both structural and synaptic plasticity. To understand the biological mechanisms that underpin such plasticity requires the development of cell level models that capture the mu...

Descripción completa

Detalles Bibliográficos
Autores principales: Wade, John J., McDaid, Liam J., Harkin, Jim, Crunelli, Vincenzo, Kelso, J. A. Scott
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248449/
https://www.ncbi.nlm.nih.gov/pubmed/22242121
http://dx.doi.org/10.1371/journal.pone.0029445
_version_ 1782220246038347776
author Wade, John J.
McDaid, Liam J.
Harkin, Jim
Crunelli, Vincenzo
Kelso, J. A. Scott
author_facet Wade, John J.
McDaid, Liam J.
Harkin, Jim
Crunelli, Vincenzo
Kelso, J. A. Scott
author_sort Wade, John J.
collection PubMed
description In recent years research suggests that astrocyte networks, in addition to nutrient and waste processing functions, regulate both structural and synaptic plasticity. To understand the biological mechanisms that underpin such plasticity requires the development of cell level models that capture the mutual interaction between astrocytes and neurons. This paper presents a detailed model of bidirectional signaling between astrocytes and neurons (the astrocyte-neuron model or AN model) which yields new insights into the computational role of astrocyte-neuronal coupling. From a set of modeling studies we demonstrate two significant findings. Firstly, that spatial signaling via astrocytes can relay a “learning signal” to remote synaptic sites. Results show that slow inward currents cause synchronized postsynaptic activity in remote neurons and subsequently allow Spike-Timing-Dependent Plasticity based learning to occur at the associated synapses. Secondly, that bidirectional communication between neurons and astrocytes underpins dynamic coordination between neuron clusters. Although our composite AN model is presently applied to simplified neural structures and limited to coordination between localized neurons, the principle (which embodies structural, functional and dynamic complexity), and the modeling strategy may be extended to coordination among remote neuron clusters.
format Online
Article
Text
id pubmed-3248449
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-32484492012-01-12 Bidirectional Coupling between Astrocytes and Neurons Mediates Learning and Dynamic Coordination in the Brain: A Multiple Modeling Approach Wade, John J. McDaid, Liam J. Harkin, Jim Crunelli, Vincenzo Kelso, J. A. Scott PLoS One Research Article In recent years research suggests that astrocyte networks, in addition to nutrient and waste processing functions, regulate both structural and synaptic plasticity. To understand the biological mechanisms that underpin such plasticity requires the development of cell level models that capture the mutual interaction between astrocytes and neurons. This paper presents a detailed model of bidirectional signaling between astrocytes and neurons (the astrocyte-neuron model or AN model) which yields new insights into the computational role of astrocyte-neuronal coupling. From a set of modeling studies we demonstrate two significant findings. Firstly, that spatial signaling via astrocytes can relay a “learning signal” to remote synaptic sites. Results show that slow inward currents cause synchronized postsynaptic activity in remote neurons and subsequently allow Spike-Timing-Dependent Plasticity based learning to occur at the associated synapses. Secondly, that bidirectional communication between neurons and astrocytes underpins dynamic coordination between neuron clusters. Although our composite AN model is presently applied to simplified neural structures and limited to coordination between localized neurons, the principle (which embodies structural, functional and dynamic complexity), and the modeling strategy may be extended to coordination among remote neuron clusters. Public Library of Science 2011-12-29 /pmc/articles/PMC3248449/ /pubmed/22242121 http://dx.doi.org/10.1371/journal.pone.0029445 Text en Wade et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wade, John J.
McDaid, Liam J.
Harkin, Jim
Crunelli, Vincenzo
Kelso, J. A. Scott
Bidirectional Coupling between Astrocytes and Neurons Mediates Learning and Dynamic Coordination in the Brain: A Multiple Modeling Approach
title Bidirectional Coupling between Astrocytes and Neurons Mediates Learning and Dynamic Coordination in the Brain: A Multiple Modeling Approach
title_full Bidirectional Coupling between Astrocytes and Neurons Mediates Learning and Dynamic Coordination in the Brain: A Multiple Modeling Approach
title_fullStr Bidirectional Coupling between Astrocytes and Neurons Mediates Learning and Dynamic Coordination in the Brain: A Multiple Modeling Approach
title_full_unstemmed Bidirectional Coupling between Astrocytes and Neurons Mediates Learning and Dynamic Coordination in the Brain: A Multiple Modeling Approach
title_short Bidirectional Coupling between Astrocytes and Neurons Mediates Learning and Dynamic Coordination in the Brain: A Multiple Modeling Approach
title_sort bidirectional coupling between astrocytes and neurons mediates learning and dynamic coordination in the brain: a multiple modeling approach
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248449/
https://www.ncbi.nlm.nih.gov/pubmed/22242121
http://dx.doi.org/10.1371/journal.pone.0029445
work_keys_str_mv AT wadejohnj bidirectionalcouplingbetweenastrocytesandneuronsmediateslearninganddynamiccoordinationinthebrainamultiplemodelingapproach
AT mcdaidliamj bidirectionalcouplingbetweenastrocytesandneuronsmediateslearninganddynamiccoordinationinthebrainamultiplemodelingapproach
AT harkinjim bidirectionalcouplingbetweenastrocytesandneuronsmediateslearninganddynamiccoordinationinthebrainamultiplemodelingapproach
AT crunellivincenzo bidirectionalcouplingbetweenastrocytesandneuronsmediateslearninganddynamiccoordinationinthebrainamultiplemodelingapproach
AT kelsojascott bidirectionalcouplingbetweenastrocytesandneuronsmediateslearninganddynamiccoordinationinthebrainamultiplemodelingapproach