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...

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Main Authors: Kendra S Burbank, Gabriel Kreiman
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS Computational Biology
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22396630/?tool=EBI
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spelling doaj-0beb46d041204183aecd966c2361afb02021-04-21T15:09:49ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582012-01-0183e100239310.1371/journal.pcbi.1002393Depression-biased reverse plasticity rule is required for stable learning at top-down connections.Kendra S BurbankGabriel KreimanTop-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.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22396630/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Kendra S Burbank
Gabriel Kreiman
spellingShingle Kendra S Burbank
Gabriel Kreiman
Depression-biased reverse plasticity rule is required for stable learning at top-down connections.
PLoS Computational Biology
author_facet Kendra S Burbank
Gabriel Kreiman
author_sort Kendra S Burbank
title 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_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_sort depression-biased reverse plasticity rule is required for stable learning at top-down connections.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2012-01-01
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.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22396630/?tool=EBI
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