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Depression-Biased Reverse Plasticity Rule Is Required for Stable Learning at Top-Down Connections
Top-down synapses are ubiquitous throughout neocortex and play a central role in cognition, yet little is known about their development and specificity. During sensory experience, lower neocortical areas are activated before higher ones, causing top-down synapses to experience a preponderance of pos...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3291526/ https://www.ncbi.nlm.nih.gov/pubmed/22396630 http://dx.doi.org/10.1371/journal.pcbi.1002393 |
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author | Burbank, Kendra S. Kreiman, Gabriel |
author_facet | Burbank, Kendra S. Kreiman, Gabriel |
author_sort | Burbank, Kendra S. |
collection | PubMed |
description | Top-down synapses are ubiquitous throughout neocortex and play a central role in cognition, yet little is known about their development and specificity. During sensory experience, lower neocortical areas are activated before higher ones, causing top-down synapses to experience a preponderance of post-synaptic activity preceding pre-synaptic activity. This timing pattern is the opposite of that experienced by bottom-up synapses, which suggests that different versions of spike-timing dependent synaptic plasticity (STDP) rules may be required at top-down synapses. We consider a two-layer neural network model and investigate which STDP rules can lead to a distribution of top-down synaptic weights that is stable, diverse and avoids strong loops. We introduce a temporally reversed rule (rSTDP) where top-down synapses are potentiated if post-synaptic activity precedes pre-synaptic activity. Combining analytical work and integrate-and-fire simulations, we show that only depression-biased rSTDP (and not classical STDP) produces stable and diverse top-down weights. The conclusions did not change upon addition of homeostatic mechanisms, multiplicative STDP rules or weak external input to the top neurons. Our prediction for rSTDP at top-down synapses, which are distally located, is supported by recent neurophysiological evidence showing the existence of temporally reversed STDP in synapses that are distal to the post-synaptic cell body. |
format | Online Article Text |
id | pubmed-3291526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32915262012-03-06 Depression-Biased Reverse Plasticity Rule Is Required for Stable Learning at Top-Down Connections Burbank, Kendra S. Kreiman, Gabriel PLoS Comput Biol Research Article Top-down synapses are ubiquitous throughout neocortex and play a central role in cognition, yet little is known about their development and specificity. During sensory experience, lower neocortical areas are activated before higher ones, causing top-down synapses to experience a preponderance of post-synaptic activity preceding pre-synaptic activity. This timing pattern is the opposite of that experienced by bottom-up synapses, which suggests that different versions of spike-timing dependent synaptic plasticity (STDP) rules may be required at top-down synapses. We consider a two-layer neural network model and investigate which STDP rules can lead to a distribution of top-down synaptic weights that is stable, diverse and avoids strong loops. We introduce a temporally reversed rule (rSTDP) where top-down synapses are potentiated if post-synaptic activity precedes pre-synaptic activity. Combining analytical work and integrate-and-fire simulations, we show that only depression-biased rSTDP (and not classical STDP) produces stable and diverse top-down weights. The conclusions did not change upon addition of homeostatic mechanisms, multiplicative STDP rules or weak external input to the top neurons. Our prediction for rSTDP at top-down synapses, which are distally located, is supported by recent neurophysiological evidence showing the existence of temporally reversed STDP in synapses that are distal to the post-synaptic cell body. Public Library of Science 2012-03-01 /pmc/articles/PMC3291526/ /pubmed/22396630 http://dx.doi.org/10.1371/journal.pcbi.1002393 Text en Burbank, Kreiman. 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 Burbank, Kendra S. Kreiman, Gabriel Depression-Biased Reverse Plasticity Rule Is Required for Stable Learning at Top-Down Connections |
title | Depression-Biased Reverse Plasticity Rule Is Required for Stable Learning at Top-Down Connections |
title_full | Depression-Biased Reverse Plasticity Rule Is Required for Stable Learning at Top-Down Connections |
title_fullStr | Depression-Biased Reverse Plasticity Rule Is Required for Stable Learning at Top-Down Connections |
title_full_unstemmed | Depression-Biased Reverse Plasticity Rule Is Required for Stable Learning at Top-Down Connections |
title_short | Depression-Biased Reverse Plasticity Rule Is Required for Stable Learning at Top-Down Connections |
title_sort | depression-biased reverse plasticity rule is required for stable learning at top-down connections |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3291526/ https://www.ncbi.nlm.nih.gov/pubmed/22396630 http://dx.doi.org/10.1371/journal.pcbi.1002393 |
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