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Evolution of neural activity in circuits bridging sensory and abstract knowledge
The ability to associate sensory stimuli with abstract classes is critical for survival. How are these associations implemented in brain circuits? And what governs how neural activity evolves during abstract knowledge acquisition? To investigate these questions, we consider a circuit model that lear...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9991064/ https://www.ncbi.nlm.nih.gov/pubmed/36881019 http://dx.doi.org/10.7554/eLife.79908 |
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author | Mastrogiuseppe, Francesca Hiratani, Naoki Latham, Peter |
author_facet | Mastrogiuseppe, Francesca Hiratani, Naoki Latham, Peter |
author_sort | Mastrogiuseppe, Francesca |
collection | PubMed |
description | The ability to associate sensory stimuli with abstract classes is critical for survival. How are these associations implemented in brain circuits? And what governs how neural activity evolves during abstract knowledge acquisition? To investigate these questions, we consider a circuit model that learns to map sensory input to abstract classes via gradient-descent synaptic plasticity. We focus on typical neuroscience tasks (simple, and context-dependent, categorization), and study how both synaptic connectivity and neural activity evolve during learning. To make contact with the current generation of experiments, we analyze activity via standard measures such as selectivity, correlations, and tuning symmetry. We find that the model is able to recapitulate experimental observations, including seemingly disparate ones. We determine how, in the model, the behaviour of these measures depends on details of the circuit and the task. These dependencies make experimentally testable predictions about the circuitry supporting abstract knowledge acquisition in the brain. |
format | Online Article Text |
id | pubmed-9991064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-99910642023-03-08 Evolution of neural activity in circuits bridging sensory and abstract knowledge Mastrogiuseppe, Francesca Hiratani, Naoki Latham, Peter eLife Neuroscience The ability to associate sensory stimuli with abstract classes is critical for survival. How are these associations implemented in brain circuits? And what governs how neural activity evolves during abstract knowledge acquisition? To investigate these questions, we consider a circuit model that learns to map sensory input to abstract classes via gradient-descent synaptic plasticity. We focus on typical neuroscience tasks (simple, and context-dependent, categorization), and study how both synaptic connectivity and neural activity evolve during learning. To make contact with the current generation of experiments, we analyze activity via standard measures such as selectivity, correlations, and tuning symmetry. We find that the model is able to recapitulate experimental observations, including seemingly disparate ones. We determine how, in the model, the behaviour of these measures depends on details of the circuit and the task. These dependencies make experimentally testable predictions about the circuitry supporting abstract knowledge acquisition in the brain. eLife Sciences Publications, Ltd 2023-03-07 /pmc/articles/PMC9991064/ /pubmed/36881019 http://dx.doi.org/10.7554/eLife.79908 Text en © 2023, Mastrogiuseppe et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Mastrogiuseppe, Francesca Hiratani, Naoki Latham, Peter Evolution of neural activity in circuits bridging sensory and abstract knowledge |
title | Evolution of neural activity in circuits bridging sensory and abstract knowledge |
title_full | Evolution of neural activity in circuits bridging sensory and abstract knowledge |
title_fullStr | Evolution of neural activity in circuits bridging sensory and abstract knowledge |
title_full_unstemmed | Evolution of neural activity in circuits bridging sensory and abstract knowledge |
title_short | Evolution of neural activity in circuits bridging sensory and abstract knowledge |
title_sort | evolution of neural activity in circuits bridging sensory and abstract knowledge |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9991064/ https://www.ncbi.nlm.nih.gov/pubmed/36881019 http://dx.doi.org/10.7554/eLife.79908 |
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