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Interplay between global and pathway-specific synaptic plasticity in CA1 pyramidal cells

Mechanisms underlying information storage have been depicted for global cell-wide and pathway-specific synaptic plasticity. Yet, little is known how these forms of plasticity interact to enhance synaptic competition and network stability. We examined synaptic interactions between apical and basal de...

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Autores principales: Berberich, Sven, Pohle, Jörg, Pollard, Marie, Barroso-Flores, Janet, Köhr, Georg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719010/
https://www.ncbi.nlm.nih.gov/pubmed/29213058
http://dx.doi.org/10.1038/s41598-017-17161-z
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author Berberich, Sven
Pohle, Jörg
Pollard, Marie
Barroso-Flores, Janet
Köhr, Georg
author_facet Berberich, Sven
Pohle, Jörg
Pollard, Marie
Barroso-Flores, Janet
Köhr, Georg
author_sort Berberich, Sven
collection PubMed
description Mechanisms underlying information storage have been depicted for global cell-wide and pathway-specific synaptic plasticity. Yet, little is known how these forms of plasticity interact to enhance synaptic competition and network stability. We examined synaptic interactions between apical and basal dendrites of CA1 pyramidal neurons in mouse hippocampal slices. Bursts (50 Hz) of three action potentials (AP-bursts) paired with preceding presynaptic stimulation in stratum radiatum specifically led to LTP of the paired pathway in adult mice (P75). At adolescence (P28), an increase in burst frequency (>50 Hz) was required to gain timing-dependent LTP. Surprisingly, paired radiatum and unpaired oriens pathway potentiated, unless the pre-post delay was shortened from 10 to 5 ms, which selectively potentiated paired radiatum pathway, since unpaired oriens pathway decreased back to baseline. Conversely, the exact same 5 ms pairing in stratum oriens potentiated both pathways, as did AP-bursts alone, which potentiated synaptic efficacy as well as current-evoked postsynaptic spiking. L-type voltage-gated Ca(2+) channels were involved in mediating synaptic potentiation in oriens, whereas NMDA and adenosine receptors counteracted unpaired stratum oriens potentiation following pairing in stratum radiatum. This asymmetric plasticity uncovers important insights into alterations of synaptic efficacy and intrinsic neuronal excitability for pathways that convey hippocampal and extra-hippocampal information.
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spelling pubmed-57190102017-12-08 Interplay between global and pathway-specific synaptic plasticity in CA1 pyramidal cells Berberich, Sven Pohle, Jörg Pollard, Marie Barroso-Flores, Janet Köhr, Georg Sci Rep Article Mechanisms underlying information storage have been depicted for global cell-wide and pathway-specific synaptic plasticity. Yet, little is known how these forms of plasticity interact to enhance synaptic competition and network stability. We examined synaptic interactions between apical and basal dendrites of CA1 pyramidal neurons in mouse hippocampal slices. Bursts (50 Hz) of three action potentials (AP-bursts) paired with preceding presynaptic stimulation in stratum radiatum specifically led to LTP of the paired pathway in adult mice (P75). At adolescence (P28), an increase in burst frequency (>50 Hz) was required to gain timing-dependent LTP. Surprisingly, paired radiatum and unpaired oriens pathway potentiated, unless the pre-post delay was shortened from 10 to 5 ms, which selectively potentiated paired radiatum pathway, since unpaired oriens pathway decreased back to baseline. Conversely, the exact same 5 ms pairing in stratum oriens potentiated both pathways, as did AP-bursts alone, which potentiated synaptic efficacy as well as current-evoked postsynaptic spiking. L-type voltage-gated Ca(2+) channels were involved in mediating synaptic potentiation in oriens, whereas NMDA and adenosine receptors counteracted unpaired stratum oriens potentiation following pairing in stratum radiatum. This asymmetric plasticity uncovers important insights into alterations of synaptic efficacy and intrinsic neuronal excitability for pathways that convey hippocampal and extra-hippocampal information. Nature Publishing Group UK 2017-12-06 /pmc/articles/PMC5719010/ /pubmed/29213058 http://dx.doi.org/10.1038/s41598-017-17161-z Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Berberich, Sven
Pohle, Jörg
Pollard, Marie
Barroso-Flores, Janet
Köhr, Georg
Interplay between global and pathway-specific synaptic plasticity in CA1 pyramidal cells
title Interplay between global and pathway-specific synaptic plasticity in CA1 pyramidal cells
title_full Interplay between global and pathway-specific synaptic plasticity in CA1 pyramidal cells
title_fullStr Interplay between global and pathway-specific synaptic plasticity in CA1 pyramidal cells
title_full_unstemmed Interplay between global and pathway-specific synaptic plasticity in CA1 pyramidal cells
title_short Interplay between global and pathway-specific synaptic plasticity in CA1 pyramidal cells
title_sort interplay between global and pathway-specific synaptic plasticity in ca1 pyramidal cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719010/
https://www.ncbi.nlm.nih.gov/pubmed/29213058
http://dx.doi.org/10.1038/s41598-017-17161-z
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