Cargando…
Pre- and postsynaptically expressed spike-timing-dependent plasticity contribute differentially to neuronal learning
A plethora of experimental studies have shown that long-term synaptic plasticity can be expressed pre- or postsynaptically depending on a range of factors such as developmental stage, synapse type, and activity patterns. The functional consequences of this diversity are not clear, although it is und...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9236267/ https://www.ncbi.nlm.nih.gov/pubmed/35700188 http://dx.doi.org/10.1371/journal.pcbi.1009409 |
_version_ | 1784736493397344256 |
---|---|
author | Mizusaki, Beatriz Eymi Pimentel Li, Sally Si Ying Costa, Rui Ponte Sjöström, Per Jesper |
author_facet | Mizusaki, Beatriz Eymi Pimentel Li, Sally Si Ying Costa, Rui Ponte Sjöström, Per Jesper |
author_sort | Mizusaki, Beatriz Eymi Pimentel |
collection | PubMed |
description | A plethora of experimental studies have shown that long-term synaptic plasticity can be expressed pre- or postsynaptically depending on a range of factors such as developmental stage, synapse type, and activity patterns. The functional consequences of this diversity are not clear, although it is understood that whereas postsynaptic expression of plasticity predominantly affects synaptic response amplitude, presynaptic expression alters both synaptic response amplitude and short-term dynamics. In most models of neuronal learning, long-term synaptic plasticity is implemented as changes in connective weights. The consideration of long-term plasticity as a fixed change in amplitude corresponds more closely to post- than to presynaptic expression, which means theoretical outcomes based on this choice of implementation may have a postsynaptic bias. To explore the functional implications of the diversity of expression of long-term synaptic plasticity, we adapted a model of long-term plasticity, more specifically spike-timing-dependent plasticity (STDP), such that it was expressed either independently pre- or postsynaptically, or in a mixture of both ways. We compared pair-based standard STDP models and a biologically tuned triplet STDP model, and investigated the outcomes in a minimal setting, using two different learning schemes: in the first, inputs were triggered at different latencies, and in the second a subset of inputs were temporally correlated. We found that presynaptic changes adjusted the speed of learning, while postsynaptic expression was more efficient at regulating spike timing and frequency. When combining both expression loci, postsynaptic changes amplified the response range, while presynaptic plasticity allowed control over postsynaptic firing rates, potentially providing a form of activity homeostasis. Our findings highlight how the seemingly innocuous choice of implementing synaptic plasticity by single weight modification may unwittingly introduce a postsynaptic bias in modelling outcomes. We conclude that pre- and postsynaptically expressed plasticity are not interchangeable, but enable complimentary functions. |
format | Online Article Text |
id | pubmed-9236267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-92362672022-06-28 Pre- and postsynaptically expressed spike-timing-dependent plasticity contribute differentially to neuronal learning Mizusaki, Beatriz Eymi Pimentel Li, Sally Si Ying Costa, Rui Ponte Sjöström, Per Jesper PLoS Comput Biol Research Article A plethora of experimental studies have shown that long-term synaptic plasticity can be expressed pre- or postsynaptically depending on a range of factors such as developmental stage, synapse type, and activity patterns. The functional consequences of this diversity are not clear, although it is understood that whereas postsynaptic expression of plasticity predominantly affects synaptic response amplitude, presynaptic expression alters both synaptic response amplitude and short-term dynamics. In most models of neuronal learning, long-term synaptic plasticity is implemented as changes in connective weights. The consideration of long-term plasticity as a fixed change in amplitude corresponds more closely to post- than to presynaptic expression, which means theoretical outcomes based on this choice of implementation may have a postsynaptic bias. To explore the functional implications of the diversity of expression of long-term synaptic plasticity, we adapted a model of long-term plasticity, more specifically spike-timing-dependent plasticity (STDP), such that it was expressed either independently pre- or postsynaptically, or in a mixture of both ways. We compared pair-based standard STDP models and a biologically tuned triplet STDP model, and investigated the outcomes in a minimal setting, using two different learning schemes: in the first, inputs were triggered at different latencies, and in the second a subset of inputs were temporally correlated. We found that presynaptic changes adjusted the speed of learning, while postsynaptic expression was more efficient at regulating spike timing and frequency. When combining both expression loci, postsynaptic changes amplified the response range, while presynaptic plasticity allowed control over postsynaptic firing rates, potentially providing a form of activity homeostasis. Our findings highlight how the seemingly innocuous choice of implementing synaptic plasticity by single weight modification may unwittingly introduce a postsynaptic bias in modelling outcomes. We conclude that pre- and postsynaptically expressed plasticity are not interchangeable, but enable complimentary functions. Public Library of Science 2022-06-14 /pmc/articles/PMC9236267/ /pubmed/35700188 http://dx.doi.org/10.1371/journal.pcbi.1009409 Text en © 2022 Mizusaki et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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 Mizusaki, Beatriz Eymi Pimentel Li, Sally Si Ying Costa, Rui Ponte Sjöström, Per Jesper Pre- and postsynaptically expressed spike-timing-dependent plasticity contribute differentially to neuronal learning |
title | Pre- and postsynaptically expressed spike-timing-dependent plasticity contribute differentially to neuronal learning |
title_full | Pre- and postsynaptically expressed spike-timing-dependent plasticity contribute differentially to neuronal learning |
title_fullStr | Pre- and postsynaptically expressed spike-timing-dependent plasticity contribute differentially to neuronal learning |
title_full_unstemmed | Pre- and postsynaptically expressed spike-timing-dependent plasticity contribute differentially to neuronal learning |
title_short | Pre- and postsynaptically expressed spike-timing-dependent plasticity contribute differentially to neuronal learning |
title_sort | pre- and postsynaptically expressed spike-timing-dependent plasticity contribute differentially to neuronal learning |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9236267/ https://www.ncbi.nlm.nih.gov/pubmed/35700188 http://dx.doi.org/10.1371/journal.pcbi.1009409 |
work_keys_str_mv | AT mizusakibeatrizeymipimentel preandpostsynapticallyexpressedspiketimingdependentplasticitycontributedifferentiallytoneuronallearning AT lisallysiying preandpostsynapticallyexpressedspiketimingdependentplasticitycontributedifferentiallytoneuronallearning AT costaruiponte preandpostsynapticallyexpressedspiketimingdependentplasticitycontributedifferentiallytoneuronallearning AT sjostromperjesper preandpostsynapticallyexpressedspiketimingdependentplasticitycontributedifferentiallytoneuronallearning |