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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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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. |
format | Online Article Text |
id | pubmed-3827605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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