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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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 |
work_keys_str_mv |
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