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Cell-specific synaptic plasticity induced by network oscillations
Gamma rhythms are known to contribute to the process of memory encoding. However, little is known about the underlying mechanisms at the molecular, cellular and network levels. Using local field potential recording in awake behaving mice and concomitant field potential and whole-cell recordings in s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929000/ https://www.ncbi.nlm.nih.gov/pubmed/27218453 http://dx.doi.org/10.7554/eLife.14912 |
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author | Zarnadze, Shota Bäuerle, Peter Santos-Torres, Julio Böhm, Claudia Schmitz, Dietmar Geiger, Jörg RP Dugladze, Tamar Gloveli, Tengis |
author_facet | Zarnadze, Shota Bäuerle, Peter Santos-Torres, Julio Böhm, Claudia Schmitz, Dietmar Geiger, Jörg RP Dugladze, Tamar Gloveli, Tengis |
author_sort | Zarnadze, Shota |
collection | PubMed |
description | Gamma rhythms are known to contribute to the process of memory encoding. However, little is known about the underlying mechanisms at the molecular, cellular and network levels. Using local field potential recording in awake behaving mice and concomitant field potential and whole-cell recordings in slice preparations we found that gamma rhythms lead to activity-dependent modification of hippocampal networks, including alterations in sharp wave-ripple complexes. Network plasticity, expressed as long-lasting increases in sharp wave-associated synaptic currents, exhibits enhanced excitatory synaptic strength in pyramidal cells that is induced postsynaptically and depends on metabotropic glutamate receptor-5 activation. In sharp contrast, alteration of inhibitory synaptic strength is independent of postsynaptic activation and less pronounced. Further, we found a cell type-specific, directionally biased synaptic plasticity of two major types of GABAergic cells, parvalbumin- and cholecystokinin-expressing interneurons. Thus, we propose that gamma frequency oscillations represent a network state that introduces long-lasting synaptic plasticity in a cell-specific manner. DOI: http://dx.doi.org/10.7554/eLife.14912.001 |
format | Online Article Text |
id | pubmed-4929000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49290002016-07-05 Cell-specific synaptic plasticity induced by network oscillations Zarnadze, Shota Bäuerle, Peter Santos-Torres, Julio Böhm, Claudia Schmitz, Dietmar Geiger, Jörg RP Dugladze, Tamar Gloveli, Tengis eLife Neuroscience Gamma rhythms are known to contribute to the process of memory encoding. However, little is known about the underlying mechanisms at the molecular, cellular and network levels. Using local field potential recording in awake behaving mice and concomitant field potential and whole-cell recordings in slice preparations we found that gamma rhythms lead to activity-dependent modification of hippocampal networks, including alterations in sharp wave-ripple complexes. Network plasticity, expressed as long-lasting increases in sharp wave-associated synaptic currents, exhibits enhanced excitatory synaptic strength in pyramidal cells that is induced postsynaptically and depends on metabotropic glutamate receptor-5 activation. In sharp contrast, alteration of inhibitory synaptic strength is independent of postsynaptic activation and less pronounced. Further, we found a cell type-specific, directionally biased synaptic plasticity of two major types of GABAergic cells, parvalbumin- and cholecystokinin-expressing interneurons. Thus, we propose that gamma frequency oscillations represent a network state that introduces long-lasting synaptic plasticity in a cell-specific manner. DOI: http://dx.doi.org/10.7554/eLife.14912.001 eLife Sciences Publications, Ltd 2016-05-24 /pmc/articles/PMC4929000/ /pubmed/27218453 http://dx.doi.org/10.7554/eLife.14912 Text en © 2016, Zarnadze et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Zarnadze, Shota Bäuerle, Peter Santos-Torres, Julio Böhm, Claudia Schmitz, Dietmar Geiger, Jörg RP Dugladze, Tamar Gloveli, Tengis Cell-specific synaptic plasticity induced by network oscillations |
title | Cell-specific synaptic plasticity induced by network oscillations |
title_full | Cell-specific synaptic plasticity induced by network oscillations |
title_fullStr | Cell-specific synaptic plasticity induced by network oscillations |
title_full_unstemmed | Cell-specific synaptic plasticity induced by network oscillations |
title_short | Cell-specific synaptic plasticity induced by network oscillations |
title_sort | cell-specific synaptic plasticity induced by network oscillations |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929000/ https://www.ncbi.nlm.nih.gov/pubmed/27218453 http://dx.doi.org/10.7554/eLife.14912 |
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