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A functional spiking-neuron model of activity-silent working memory in humans based on calcium-mediated short-term synaptic plasticity
In this paper, we present a functional spiking-neuron model of human working memory (WM). This model combines neural firing for encoding of information with activity-silent maintenance. While it used to be widely assumed that information in WM is maintained through persistent recurrent activity, rec...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282629/ https://www.ncbi.nlm.nih.gov/pubmed/32516337 http://dx.doi.org/10.1371/journal.pcbi.1007936 |
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author | Pals, Matthijs Stewart, Terrence C. Akyürek, Elkan G. Borst, Jelmer P. |
author_facet | Pals, Matthijs Stewart, Terrence C. Akyürek, Elkan G. Borst, Jelmer P. |
author_sort | Pals, Matthijs |
collection | PubMed |
description | In this paper, we present a functional spiking-neuron model of human working memory (WM). This model combines neural firing for encoding of information with activity-silent maintenance. While it used to be widely assumed that information in WM is maintained through persistent recurrent activity, recent studies have shown that information can be maintained without persistent firing; instead, information can be stored in activity-silent states. A candidate mechanism underlying this type of storage is short-term synaptic plasticity (STSP), by which the strength of connections between neurons rapidly changes to encode new information. To demonstrate that STSP can lead to functional behavior, we integrated STSP by means of calcium-mediated synaptic facilitation in a large-scale spiking-neuron model and added a decision mechanism. The model was used to simulate a recent study that measured behavior and EEG activity of participants in three delayed-response tasks. In these tasks, one or two visual gratings had to be maintained in WM, and compared to subsequent probes. The original study demonstrated that WM contents and its priority status could be decoded from neural activity elicited by a task-irrelevant stimulus displayed during the activity-silent maintenance period. In support of our model, we show that it can perform these tasks, and that both its behavior as well as its neural representations are in agreement with the human data. We conclude that information in WM can be effectively maintained in activity-silent states by means of calcium-mediated STSP. |
format | Online Article Text |
id | pubmed-7282629 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-72826292020-06-17 A functional spiking-neuron model of activity-silent working memory in humans based on calcium-mediated short-term synaptic plasticity Pals, Matthijs Stewart, Terrence C. Akyürek, Elkan G. Borst, Jelmer P. PLoS Comput Biol Research Article In this paper, we present a functional spiking-neuron model of human working memory (WM). This model combines neural firing for encoding of information with activity-silent maintenance. While it used to be widely assumed that information in WM is maintained through persistent recurrent activity, recent studies have shown that information can be maintained without persistent firing; instead, information can be stored in activity-silent states. A candidate mechanism underlying this type of storage is short-term synaptic plasticity (STSP), by which the strength of connections between neurons rapidly changes to encode new information. To demonstrate that STSP can lead to functional behavior, we integrated STSP by means of calcium-mediated synaptic facilitation in a large-scale spiking-neuron model and added a decision mechanism. The model was used to simulate a recent study that measured behavior and EEG activity of participants in three delayed-response tasks. In these tasks, one or two visual gratings had to be maintained in WM, and compared to subsequent probes. The original study demonstrated that WM contents and its priority status could be decoded from neural activity elicited by a task-irrelevant stimulus displayed during the activity-silent maintenance period. In support of our model, we show that it can perform these tasks, and that both its behavior as well as its neural representations are in agreement with the human data. We conclude that information in WM can be effectively maintained in activity-silent states by means of calcium-mediated STSP. Public Library of Science 2020-06-09 /pmc/articles/PMC7282629/ /pubmed/32516337 http://dx.doi.org/10.1371/journal.pcbi.1007936 Text en © 2020 Pals 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 (http://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 Pals, Matthijs Stewart, Terrence C. Akyürek, Elkan G. Borst, Jelmer P. A functional spiking-neuron model of activity-silent working memory in humans based on calcium-mediated short-term synaptic plasticity |
title | A functional spiking-neuron model of activity-silent working memory in humans based on calcium-mediated short-term synaptic plasticity |
title_full | A functional spiking-neuron model of activity-silent working memory in humans based on calcium-mediated short-term synaptic plasticity |
title_fullStr | A functional spiking-neuron model of activity-silent working memory in humans based on calcium-mediated short-term synaptic plasticity |
title_full_unstemmed | A functional spiking-neuron model of activity-silent working memory in humans based on calcium-mediated short-term synaptic plasticity |
title_short | A functional spiking-neuron model of activity-silent working memory in humans based on calcium-mediated short-term synaptic plasticity |
title_sort | functional spiking-neuron model of activity-silent working memory in humans based on calcium-mediated short-term synaptic plasticity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282629/ https://www.ncbi.nlm.nih.gov/pubmed/32516337 http://dx.doi.org/10.1371/journal.pcbi.1007936 |
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