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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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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. |
format | Online Article Text |
id | pubmed-3636028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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