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Long-term plasticity determines the postsynaptic response to correlated afferents with multivesicular short-term synaptic depression
Synchrony in a presynaptic population leads to correlations in vesicle occupancy at the active sites for neurotransmitter release. The number of independent release sites per presynaptic neuron, a synaptic parameter recently shown to be modified during long-term plasticity, will modulate these corre...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906582/ https://www.ncbi.nlm.nih.gov/pubmed/24523691 http://dx.doi.org/10.3389/fncom.2014.00002 |
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author | Bird, Alex D. Richardson, Magnus J. E. |
author_facet | Bird, Alex D. Richardson, Magnus J. E. |
author_sort | Bird, Alex D. |
collection | PubMed |
description | Synchrony in a presynaptic population leads to correlations in vesicle occupancy at the active sites for neurotransmitter release. The number of independent release sites per presynaptic neuron, a synaptic parameter recently shown to be modified during long-term plasticity, will modulate these correlations and therefore have a significant effect on the firing rate of the postsynaptic neuron. To understand how correlations from synaptic dynamics and from presynaptic synchrony shape the postsynaptic response, we study a model of multiple release site short-term plasticity and derive exact results for the crosscorrelation function of vesicle occupancy and neurotransmitter release, as well as the postsynaptic voltage variance. Using approximate forms for the postsynaptic firing rate in the limits of low and high correlations, we demonstrate that short-term depression leads to a maximum response for an intermediate number of presynaptic release sites, and that this leads to a tuning-curve response peaked at an optimal presynaptic synchrony set by the number of neurotransmitter release sites per presynaptic neuron. These effects arise because, above a certain level of correlation, activity in the presynaptic population is overly strong resulting in wastage of the pool of releasable neurotransmitter. As the nervous system operates under constraints of efficient metabolism it is likely that this phenomenon provides an activity-dependent constraint on network architecture. |
format | Online Article Text |
id | pubmed-3906582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-39065822014-02-12 Long-term plasticity determines the postsynaptic response to correlated afferents with multivesicular short-term synaptic depression Bird, Alex D. Richardson, Magnus J. E. Front Comput Neurosci Neuroscience Synchrony in a presynaptic population leads to correlations in vesicle occupancy at the active sites for neurotransmitter release. The number of independent release sites per presynaptic neuron, a synaptic parameter recently shown to be modified during long-term plasticity, will modulate these correlations and therefore have a significant effect on the firing rate of the postsynaptic neuron. To understand how correlations from synaptic dynamics and from presynaptic synchrony shape the postsynaptic response, we study a model of multiple release site short-term plasticity and derive exact results for the crosscorrelation function of vesicle occupancy and neurotransmitter release, as well as the postsynaptic voltage variance. Using approximate forms for the postsynaptic firing rate in the limits of low and high correlations, we demonstrate that short-term depression leads to a maximum response for an intermediate number of presynaptic release sites, and that this leads to a tuning-curve response peaked at an optimal presynaptic synchrony set by the number of neurotransmitter release sites per presynaptic neuron. These effects arise because, above a certain level of correlation, activity in the presynaptic population is overly strong resulting in wastage of the pool of releasable neurotransmitter. As the nervous system operates under constraints of efficient metabolism it is likely that this phenomenon provides an activity-dependent constraint on network architecture. Frontiers Media S.A. 2014-01-30 /pmc/articles/PMC3906582/ /pubmed/24523691 http://dx.doi.org/10.3389/fncom.2014.00002 Text en Copyright © 2014 Bird and Richardson. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Bird, Alex D. Richardson, Magnus J. E. Long-term plasticity determines the postsynaptic response to correlated afferents with multivesicular short-term synaptic depression |
title | Long-term plasticity determines the postsynaptic response to correlated afferents with multivesicular short-term synaptic depression |
title_full | Long-term plasticity determines the postsynaptic response to correlated afferents with multivesicular short-term synaptic depression |
title_fullStr | Long-term plasticity determines the postsynaptic response to correlated afferents with multivesicular short-term synaptic depression |
title_full_unstemmed | Long-term plasticity determines the postsynaptic response to correlated afferents with multivesicular short-term synaptic depression |
title_short | Long-term plasticity determines the postsynaptic response to correlated afferents with multivesicular short-term synaptic depression |
title_sort | long-term plasticity determines the postsynaptic response to correlated afferents with multivesicular short-term synaptic depression |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906582/ https://www.ncbi.nlm.nih.gov/pubmed/24523691 http://dx.doi.org/10.3389/fncom.2014.00002 |
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