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Learning and stabilization of winner-take-all dynamics through interacting excitatory and inhibitory plasticity

Winner-Take-All (WTA) networks are recurrently connected populations of excitatory and inhibitory neurons that represent promising candidate microcircuits for implementing cortical computation. WTAs can perform powerful computations, ranging from signal-restoration to state-dependent processing. How...

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Autores principales: Binas, Jonathan, Rutishauser, Ueli, Indiveri, Giacomo, Pfeiffer, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086298/
https://www.ncbi.nlm.nih.gov/pubmed/25071538
http://dx.doi.org/10.3389/fncom.2014.00068
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author Binas, Jonathan
Rutishauser, Ueli
Indiveri, Giacomo
Pfeiffer, Michael
author_facet Binas, Jonathan
Rutishauser, Ueli
Indiveri, Giacomo
Pfeiffer, Michael
author_sort Binas, Jonathan
collection PubMed
description Winner-Take-All (WTA) networks are recurrently connected populations of excitatory and inhibitory neurons that represent promising candidate microcircuits for implementing cortical computation. WTAs can perform powerful computations, ranging from signal-restoration to state-dependent processing. However, such networks require fine-tuned connectivity parameters to keep the network dynamics within stable operating regimes. In this article, we show how such stability can emerge autonomously through an interaction of biologically plausible plasticity mechanisms that operate simultaneously on all excitatory and inhibitory synapses of the network. A weight-dependent plasticity rule is derived from the triplet spike-timing dependent plasticity model, and its stabilization properties in the mean-field case are analyzed using contraction theory. Our main result provides simple constraints on the plasticity rule parameters, rather than on the weights themselves, which guarantee stable WTA behavior. The plastic network we present is able to adapt to changing input conditions, and to dynamically adjust its gain, therefore exhibiting self-stabilization mechanisms that are crucial for maintaining stable operation in large networks of interconnected subunits. We show how distributed neural assemblies can adjust their parameters for stable WTA function autonomously while respecting anatomical constraints on neural wiring.
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spelling pubmed-40862982014-07-28 Learning and stabilization of winner-take-all dynamics through interacting excitatory and inhibitory plasticity Binas, Jonathan Rutishauser, Ueli Indiveri, Giacomo Pfeiffer, Michael Front Comput Neurosci Neuroscience Winner-Take-All (WTA) networks are recurrently connected populations of excitatory and inhibitory neurons that represent promising candidate microcircuits for implementing cortical computation. WTAs can perform powerful computations, ranging from signal-restoration to state-dependent processing. However, such networks require fine-tuned connectivity parameters to keep the network dynamics within stable operating regimes. In this article, we show how such stability can emerge autonomously through an interaction of biologically plausible plasticity mechanisms that operate simultaneously on all excitatory and inhibitory synapses of the network. A weight-dependent plasticity rule is derived from the triplet spike-timing dependent plasticity model, and its stabilization properties in the mean-field case are analyzed using contraction theory. Our main result provides simple constraints on the plasticity rule parameters, rather than on the weights themselves, which guarantee stable WTA behavior. The plastic network we present is able to adapt to changing input conditions, and to dynamically adjust its gain, therefore exhibiting self-stabilization mechanisms that are crucial for maintaining stable operation in large networks of interconnected subunits. We show how distributed neural assemblies can adjust their parameters for stable WTA function autonomously while respecting anatomical constraints on neural wiring. Frontiers Media S.A. 2014-07-08 /pmc/articles/PMC4086298/ /pubmed/25071538 http://dx.doi.org/10.3389/fncom.2014.00068 Text en Copyright © 2014 Binas, Rutishauser, Indiveri and Pfeiffer. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Binas, Jonathan
Rutishauser, Ueli
Indiveri, Giacomo
Pfeiffer, Michael
Learning and stabilization of winner-take-all dynamics through interacting excitatory and inhibitory plasticity
title Learning and stabilization of winner-take-all dynamics through interacting excitatory and inhibitory plasticity
title_full Learning and stabilization of winner-take-all dynamics through interacting excitatory and inhibitory plasticity
title_fullStr Learning and stabilization of winner-take-all dynamics through interacting excitatory and inhibitory plasticity
title_full_unstemmed Learning and stabilization of winner-take-all dynamics through interacting excitatory and inhibitory plasticity
title_short Learning and stabilization of winner-take-all dynamics through interacting excitatory and inhibitory plasticity
title_sort learning and stabilization of winner-take-all dynamics through interacting excitatory and inhibitory plasticity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086298/
https://www.ncbi.nlm.nih.gov/pubmed/25071538
http://dx.doi.org/10.3389/fncom.2014.00068
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