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Synaptic weights that correlate with presynaptic selectivity increase decoding performance

The activity of neurons in the visual cortex is often characterized by tuning curves, which are thought to be shaped by Hebbian plasticity during development and sensory experience. This leads to the prediction that neural circuits should be organized such that neurons with similar functional prefer...

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Detalles Bibliográficos
Autores principales: Gallinaro, Júlia V., Scholl, Benjamin, Clopath, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10434873/
https://www.ncbi.nlm.nih.gov/pubmed/37549193
http://dx.doi.org/10.1371/journal.pcbi.1011362
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author Gallinaro, Júlia V.
Scholl, Benjamin
Clopath, Claudia
author_facet Gallinaro, Júlia V.
Scholl, Benjamin
Clopath, Claudia
author_sort Gallinaro, Júlia V.
collection PubMed
description The activity of neurons in the visual cortex is often characterized by tuning curves, which are thought to be shaped by Hebbian plasticity during development and sensory experience. This leads to the prediction that neural circuits should be organized such that neurons with similar functional preference are connected with stronger weights. In support of this idea, previous experimental and theoretical work have provided evidence for a model of the visual cortex characterized by such functional subnetworks. A recent experimental study, however, have found that the postsynaptic preferred stimulus was defined by the total number of spines activated by a given stimulus and independent of their individual strength. While this result might seem to contradict previous literature, there are many factors that define how a given synaptic input influences postsynaptic selectivity. Here, we designed a computational model in which postsynaptic functional preference is defined by the number of inputs activated by a given stimulus. Using a plasticity rule where synaptic weights tend to correlate with presynaptic selectivity, and is independent of functional-similarity between pre- and postsynaptic activity, we find that this model can be used to decode presented stimuli in a manner that is comparable to maximum likelihood inference.
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spelling pubmed-104348732023-08-18 Synaptic weights that correlate with presynaptic selectivity increase decoding performance Gallinaro, Júlia V. Scholl, Benjamin Clopath, Claudia PLoS Comput Biol Research Article The activity of neurons in the visual cortex is often characterized by tuning curves, which are thought to be shaped by Hebbian plasticity during development and sensory experience. This leads to the prediction that neural circuits should be organized such that neurons with similar functional preference are connected with stronger weights. In support of this idea, previous experimental and theoretical work have provided evidence for a model of the visual cortex characterized by such functional subnetworks. A recent experimental study, however, have found that the postsynaptic preferred stimulus was defined by the total number of spines activated by a given stimulus and independent of their individual strength. While this result might seem to contradict previous literature, there are many factors that define how a given synaptic input influences postsynaptic selectivity. Here, we designed a computational model in which postsynaptic functional preference is defined by the number of inputs activated by a given stimulus. Using a plasticity rule where synaptic weights tend to correlate with presynaptic selectivity, and is independent of functional-similarity between pre- and postsynaptic activity, we find that this model can be used to decode presented stimuli in a manner that is comparable to maximum likelihood inference. Public Library of Science 2023-08-07 /pmc/articles/PMC10434873/ /pubmed/37549193 http://dx.doi.org/10.1371/journal.pcbi.1011362 Text en © 2023 Gallinaro et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Gallinaro, Júlia V.
Scholl, Benjamin
Clopath, Claudia
Synaptic weights that correlate with presynaptic selectivity increase decoding performance
title Synaptic weights that correlate with presynaptic selectivity increase decoding performance
title_full Synaptic weights that correlate with presynaptic selectivity increase decoding performance
title_fullStr Synaptic weights that correlate with presynaptic selectivity increase decoding performance
title_full_unstemmed Synaptic weights that correlate with presynaptic selectivity increase decoding performance
title_short Synaptic weights that correlate with presynaptic selectivity increase decoding performance
title_sort synaptic weights that correlate with presynaptic selectivity increase decoding performance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10434873/
https://www.ncbi.nlm.nih.gov/pubmed/37549193
http://dx.doi.org/10.1371/journal.pcbi.1011362
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