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Synaptic Transmission Optimization Predicts Expression Loci of Long-Term Plasticity

Long-term modifications of neuronal connections are critical for reliable memory storage in the brain. However, their locus of expression—pre- or postsynaptic—is highly variable. Here we introduce a theoretical framework in which long-term plasticity performs an optimization of the postsynaptic resp...

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Detalles Bibliográficos
Autores principales: Costa, Rui Ponte, Padamsey, Zahid, D’Amour, James A., Emptage, Nigel J., Froemke, Robert C., Vogels, Tim P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626823/
https://www.ncbi.nlm.nih.gov/pubmed/28957667
http://dx.doi.org/10.1016/j.neuron.2017.09.021
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author Costa, Rui Ponte
Padamsey, Zahid
D’Amour, James A.
Emptage, Nigel J.
Froemke, Robert C.
Vogels, Tim P.
author_facet Costa, Rui Ponte
Padamsey, Zahid
D’Amour, James A.
Emptage, Nigel J.
Froemke, Robert C.
Vogels, Tim P.
author_sort Costa, Rui Ponte
collection PubMed
description Long-term modifications of neuronal connections are critical for reliable memory storage in the brain. However, their locus of expression—pre- or postsynaptic—is highly variable. Here we introduce a theoretical framework in which long-term plasticity performs an optimization of the postsynaptic response statistics toward a given mean with minimal variance. Consequently, the state of the synapse at the time of plasticity induction determines the ratio of pre- and postsynaptic modifications. Our theory explains the experimentally observed expression loci of the hippocampal and neocortical synaptic potentiation studies we examined. Moreover, the theory predicts presynaptic expression of long-term depression, consistent with experimental observations. At inhibitory synapses, the theory suggests a statistically efficient excitatory-inhibitory balance in which changes in inhibitory postsynaptic response statistics specifically target the mean excitation. Our results provide a unifying theory for understanding the expression mechanisms and functions of long-term synaptic transmission plasticity.
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spelling pubmed-56268232017-10-11 Synaptic Transmission Optimization Predicts Expression Loci of Long-Term Plasticity Costa, Rui Ponte Padamsey, Zahid D’Amour, James A. Emptage, Nigel J. Froemke, Robert C. Vogels, Tim P. Neuron Article Long-term modifications of neuronal connections are critical for reliable memory storage in the brain. However, their locus of expression—pre- or postsynaptic—is highly variable. Here we introduce a theoretical framework in which long-term plasticity performs an optimization of the postsynaptic response statistics toward a given mean with minimal variance. Consequently, the state of the synapse at the time of plasticity induction determines the ratio of pre- and postsynaptic modifications. Our theory explains the experimentally observed expression loci of the hippocampal and neocortical synaptic potentiation studies we examined. Moreover, the theory predicts presynaptic expression of long-term depression, consistent with experimental observations. At inhibitory synapses, the theory suggests a statistically efficient excitatory-inhibitory balance in which changes in inhibitory postsynaptic response statistics specifically target the mean excitation. Our results provide a unifying theory for understanding the expression mechanisms and functions of long-term synaptic transmission plasticity. Cell Press 2017-09-27 /pmc/articles/PMC5626823/ /pubmed/28957667 http://dx.doi.org/10.1016/j.neuron.2017.09.021 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Costa, Rui Ponte
Padamsey, Zahid
D’Amour, James A.
Emptage, Nigel J.
Froemke, Robert C.
Vogels, Tim P.
Synaptic Transmission Optimization Predicts Expression Loci of Long-Term Plasticity
title Synaptic Transmission Optimization Predicts Expression Loci of Long-Term Plasticity
title_full Synaptic Transmission Optimization Predicts Expression Loci of Long-Term Plasticity
title_fullStr Synaptic Transmission Optimization Predicts Expression Loci of Long-Term Plasticity
title_full_unstemmed Synaptic Transmission Optimization Predicts Expression Loci of Long-Term Plasticity
title_short Synaptic Transmission Optimization Predicts Expression Loci of Long-Term Plasticity
title_sort synaptic transmission optimization predicts expression loci of long-term plasticity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626823/
https://www.ncbi.nlm.nih.gov/pubmed/28957667
http://dx.doi.org/10.1016/j.neuron.2017.09.021
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