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Synapse-Specific Regulation Revealed at Single Synapses Is Concealed When Recording Multiple Synapses

Synaptic transmission and its activity-dependent modulation, known as synaptic plasticity, are fundamental processes in nervous system function. Neurons may receive thousands of synaptic contacts, but synaptic regulation may occur only at individual or discrete subsets of synapses, which may have im...

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Autores principales: Lines, Justin, Covelo, Ana, Gómez, Ricardo, Liu, Lan, Araque, Alfonso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703853/
https://www.ncbi.nlm.nih.gov/pubmed/29218000
http://dx.doi.org/10.3389/fncel.2017.00367
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author Lines, Justin
Covelo, Ana
Gómez, Ricardo
Liu, Lan
Araque, Alfonso
author_facet Lines, Justin
Covelo, Ana
Gómez, Ricardo
Liu, Lan
Araque, Alfonso
author_sort Lines, Justin
collection PubMed
description Synaptic transmission and its activity-dependent modulation, known as synaptic plasticity, are fundamental processes in nervous system function. Neurons may receive thousands of synaptic contacts, but synaptic regulation may occur only at individual or discrete subsets of synapses, which may have important consequences on the spatial extension of the modulation of synaptic information. Moreover, while several electrophysiological methods are used to assess synaptic transmission at different levels of observation, i.e., through local field potential and individual whole-cell recordings, their experimental limitations to detect synapse-specific modulation is poorly defined. We have investigated how well-known synapse-specific short-term plasticity, where some synapses are regulated and others left unregulated, mediated by astrocytes and endocannabinoid (eCB) signaling can be assessed at different observational levels. Using hippocampal slices, we have combined local field potential and whole-cell recordings of CA3-CA1 synaptic activity evoked by Schaffer collateral stimulation of either multiple or single synapses through bulk or minimal stimulation, respectively, to test the ability to detect short-term synaptic changes induced by eCB signaling. We also developed a mathematical model assuming a bimodal distribution of regulated and unregulated synapses based on realistic experimental data to simulate physiological results and to predict the experimental requirements of the different recording methods to detect discrete changes in subsets of synapses. We show that eCB-induced depolarization-induced suppression of excitation (DSE) and astrocyte-mediated synaptic potentiation can be observed when monitoring single or few synapses, but are statistically concealed when recording the activity of a large number of synapses. These results indicate that the electrophysiological methodology is critical to properly assess synaptic changes occurring in subsets of synapses, and they suggest that relevant synapse-specific regulatory phenomena may be experimentally undetected but may have important implications in the spatial extension of synaptic plasticity phenomena.
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spelling pubmed-57038532017-12-07 Synapse-Specific Regulation Revealed at Single Synapses Is Concealed When Recording Multiple Synapses Lines, Justin Covelo, Ana Gómez, Ricardo Liu, Lan Araque, Alfonso Front Cell Neurosci Neuroscience Synaptic transmission and its activity-dependent modulation, known as synaptic plasticity, are fundamental processes in nervous system function. Neurons may receive thousands of synaptic contacts, but synaptic regulation may occur only at individual or discrete subsets of synapses, which may have important consequences on the spatial extension of the modulation of synaptic information. Moreover, while several electrophysiological methods are used to assess synaptic transmission at different levels of observation, i.e., through local field potential and individual whole-cell recordings, their experimental limitations to detect synapse-specific modulation is poorly defined. We have investigated how well-known synapse-specific short-term plasticity, where some synapses are regulated and others left unregulated, mediated by astrocytes and endocannabinoid (eCB) signaling can be assessed at different observational levels. Using hippocampal slices, we have combined local field potential and whole-cell recordings of CA3-CA1 synaptic activity evoked by Schaffer collateral stimulation of either multiple or single synapses through bulk or minimal stimulation, respectively, to test the ability to detect short-term synaptic changes induced by eCB signaling. We also developed a mathematical model assuming a bimodal distribution of regulated and unregulated synapses based on realistic experimental data to simulate physiological results and to predict the experimental requirements of the different recording methods to detect discrete changes in subsets of synapses. We show that eCB-induced depolarization-induced suppression of excitation (DSE) and astrocyte-mediated synaptic potentiation can be observed when monitoring single or few synapses, but are statistically concealed when recording the activity of a large number of synapses. These results indicate that the electrophysiological methodology is critical to properly assess synaptic changes occurring in subsets of synapses, and they suggest that relevant synapse-specific regulatory phenomena may be experimentally undetected but may have important implications in the spatial extension of synaptic plasticity phenomena. Frontiers Media S.A. 2017-11-23 /pmc/articles/PMC5703853/ /pubmed/29218000 http://dx.doi.org/10.3389/fncel.2017.00367 Text en Copyright © 2017 Lines, Covelo, Gómez, Liu and Araque. http://creativecommons.org/licenses/by/4.0/ 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
Lines, Justin
Covelo, Ana
Gómez, Ricardo
Liu, Lan
Araque, Alfonso
Synapse-Specific Regulation Revealed at Single Synapses Is Concealed When Recording Multiple Synapses
title Synapse-Specific Regulation Revealed at Single Synapses Is Concealed When Recording Multiple Synapses
title_full Synapse-Specific Regulation Revealed at Single Synapses Is Concealed When Recording Multiple Synapses
title_fullStr Synapse-Specific Regulation Revealed at Single Synapses Is Concealed When Recording Multiple Synapses
title_full_unstemmed Synapse-Specific Regulation Revealed at Single Synapses Is Concealed When Recording Multiple Synapses
title_short Synapse-Specific Regulation Revealed at Single Synapses Is Concealed When Recording Multiple Synapses
title_sort synapse-specific regulation revealed at single synapses is concealed when recording multiple synapses
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703853/
https://www.ncbi.nlm.nih.gov/pubmed/29218000
http://dx.doi.org/10.3389/fncel.2017.00367
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