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Single-neuron criticality optimizes analog dendritic computation

Active dendritic branchlets enable the propagation of dendritic spikes, whose computational functions remain an open question. Here we propose a concrete function to the active channels in large dendritic trees. Modelling the input-output response of large active dendritic arbors subjected to comple...

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Detalles Bibliográficos
Autores principales: Gollo, Leonardo L., Kinouchi, Osame, Copelli, Mauro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3827605/
https://www.ncbi.nlm.nih.gov/pubmed/24226045
http://dx.doi.org/10.1038/srep03222
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author Gollo, Leonardo L.
Kinouchi, Osame
Copelli, Mauro
author_facet Gollo, Leonardo L.
Kinouchi, Osame
Copelli, Mauro
author_sort Gollo, Leonardo L.
collection PubMed
description Active dendritic branchlets enable the propagation of dendritic spikes, whose computational functions remain an open question. Here we propose a concrete function to the active channels in large dendritic trees. Modelling the input-output response of large active dendritic arbors subjected to complex spatio-temporal inputs and exhibiting non-stereotyped dendritic spikes, we find that the dendritic arbor can undergo a continuous phase transition from a quiescent to an active state, thereby exhibiting spontaneous and self-sustained localized activity as suggested by experiments. Analogously to the critical brain hypothesis, which states that neuronal networks self-organize near criticality to take advantage of its specific properties, here we propose that neurons with large dendritic arbors optimize their capacity to distinguish incoming stimuli at the critical state. We suggest that “computation at the edge of a phase transition” is more compatible with the view that dendritic arbors perform an analog rather than a digital dendritic computation.
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spelling pubmed-38276052013-11-15 Single-neuron criticality optimizes analog dendritic computation Gollo, Leonardo L. Kinouchi, Osame Copelli, Mauro Sci Rep Article Active dendritic branchlets enable the propagation of dendritic spikes, whose computational functions remain an open question. Here we propose a concrete function to the active channels in large dendritic trees. Modelling the input-output response of large active dendritic arbors subjected to complex spatio-temporal inputs and exhibiting non-stereotyped dendritic spikes, we find that the dendritic arbor can undergo a continuous phase transition from a quiescent to an active state, thereby exhibiting spontaneous and self-sustained localized activity as suggested by experiments. Analogously to the critical brain hypothesis, which states that neuronal networks self-organize near criticality to take advantage of its specific properties, here we propose that neurons with large dendritic arbors optimize their capacity to distinguish incoming stimuli at the critical state. We suggest that “computation at the edge of a phase transition” is more compatible with the view that dendritic arbors perform an analog rather than a digital dendritic computation. Nature Publishing Group 2013-11-14 /pmc/articles/PMC3827605/ /pubmed/24226045 http://dx.doi.org/10.1038/srep03222 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareALike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Gollo, Leonardo L.
Kinouchi, Osame
Copelli, Mauro
Single-neuron criticality optimizes analog dendritic computation
title Single-neuron criticality optimizes analog dendritic computation
title_full Single-neuron criticality optimizes analog dendritic computation
title_fullStr Single-neuron criticality optimizes analog dendritic computation
title_full_unstemmed Single-neuron criticality optimizes analog dendritic computation
title_short Single-neuron criticality optimizes analog dendritic computation
title_sort single-neuron criticality optimizes analog dendritic computation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3827605/
https://www.ncbi.nlm.nih.gov/pubmed/24226045
http://dx.doi.org/10.1038/srep03222
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