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Bayesian Computation Emerges in Generic Cortical Microcircuits through Spike-Timing-Dependent Plasticity

The principles by which networks of neurons compute, and how spike-timing dependent plasticity (STDP) of synaptic weights generates and maintains their computational function, are unknown. Preceding work has shown that soft winner-take-all (WTA) circuits, where pyramidal neurons inhibit each other v...

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Detalles Bibliográficos
Autores principales: Nessler, Bernhard, Pfeiffer, Michael, Buesing, Lars, Maass, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3636028/
https://www.ncbi.nlm.nih.gov/pubmed/23633941
http://dx.doi.org/10.1371/journal.pcbi.1003037
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author Nessler, Bernhard
Pfeiffer, Michael
Buesing, Lars
Maass, Wolfgang
author_facet Nessler, Bernhard
Pfeiffer, Michael
Buesing, Lars
Maass, Wolfgang
author_sort Nessler, Bernhard
collection PubMed
description The principles by which networks of neurons compute, and how spike-timing dependent plasticity (STDP) of synaptic weights generates and maintains their computational function, are unknown. Preceding work has shown that soft winner-take-all (WTA) circuits, where pyramidal neurons inhibit each other via interneurons, are a common motif of cortical microcircuits. We show through theoretical analysis and computer simulations that Bayesian computation is induced in these network motifs through STDP in combination with activity-dependent changes in the excitability of neurons. The fundamental components of this emergent Bayesian computation are priors that result from adaptation of neuronal excitability and implicit generative models for hidden causes that are created in the synaptic weights through STDP. In fact, a surprising result is that STDP is able to approximate a powerful principle for fitting such implicit generative models to high-dimensional spike inputs: Expectation Maximization. Our results suggest that the experimentally observed spontaneous activity and trial-to-trial variability of cortical neurons are essential features of their information processing capability, since their functional role is to represent probability distributions rather than static neural codes. Furthermore it suggests networks of Bayesian computation modules as a new model for distributed information processing in the cortex.
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spelling pubmed-36360282013-04-30 Bayesian Computation Emerges in Generic Cortical Microcircuits through Spike-Timing-Dependent Plasticity Nessler, Bernhard Pfeiffer, Michael Buesing, Lars Maass, Wolfgang PLoS Comput Biol Research Article The principles by which networks of neurons compute, and how spike-timing dependent plasticity (STDP) of synaptic weights generates and maintains their computational function, are unknown. Preceding work has shown that soft winner-take-all (WTA) circuits, where pyramidal neurons inhibit each other via interneurons, are a common motif of cortical microcircuits. We show through theoretical analysis and computer simulations that Bayesian computation is induced in these network motifs through STDP in combination with activity-dependent changes in the excitability of neurons. The fundamental components of this emergent Bayesian computation are priors that result from adaptation of neuronal excitability and implicit generative models for hidden causes that are created in the synaptic weights through STDP. In fact, a surprising result is that STDP is able to approximate a powerful principle for fitting such implicit generative models to high-dimensional spike inputs: Expectation Maximization. Our results suggest that the experimentally observed spontaneous activity and trial-to-trial variability of cortical neurons are essential features of their information processing capability, since their functional role is to represent probability distributions rather than static neural codes. Furthermore it suggests networks of Bayesian computation modules as a new model for distributed information processing in the cortex. Public Library of Science 2013-04-25 /pmc/articles/PMC3636028/ /pubmed/23633941 http://dx.doi.org/10.1371/journal.pcbi.1003037 Text en © 2013 Nessler 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
Nessler, Bernhard
Pfeiffer, Michael
Buesing, Lars
Maass, Wolfgang
Bayesian Computation Emerges in Generic Cortical Microcircuits through Spike-Timing-Dependent Plasticity
title Bayesian Computation Emerges in Generic Cortical Microcircuits through Spike-Timing-Dependent Plasticity
title_full Bayesian Computation Emerges in Generic Cortical Microcircuits through Spike-Timing-Dependent Plasticity
title_fullStr Bayesian Computation Emerges in Generic Cortical Microcircuits through Spike-Timing-Dependent Plasticity
title_full_unstemmed Bayesian Computation Emerges in Generic Cortical Microcircuits through Spike-Timing-Dependent Plasticity
title_short Bayesian Computation Emerges in Generic Cortical Microcircuits through Spike-Timing-Dependent Plasticity
title_sort bayesian computation emerges in generic cortical microcircuits through spike-timing-dependent plasticity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3636028/
https://www.ncbi.nlm.nih.gov/pubmed/23633941
http://dx.doi.org/10.1371/journal.pcbi.1003037
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