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GABA–glutamate supramammillary neurons control theta and gamma oscillations in the dentate gyrus during paradoxical (REM) sleep

Several studies suggest that neurons from the lateral region of the SuM (SuML) innervating the dorsal dentate gyrus (DG) display a dual GABAergic and glutamatergic transmission and are specifically activated during paradoxical (REM) sleep (PS). The objective of the present study is to characterize t...

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Autores principales: Billwiller, Francesca, Castillo, Laura, Elseedy, Heba, Ivanov, Anton Ivanovich, Scapula, Jennyfer, Ghestem, Antoine, Carponcy, Julien, Libourel, Paul Antoine, Bras, Hélène, Abdelmeguid, Nabila ElSayed, Krook-Magnuson, Esther, Soltesz, Ivan, Bernard, Christophe, Luppi, Pierre-Hervé, Esclapez, Monique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674372/
https://www.ncbi.nlm.nih.gov/pubmed/32970253
http://dx.doi.org/10.1007/s00429-020-02146-y
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author Billwiller, Francesca
Castillo, Laura
Elseedy, Heba
Ivanov, Anton Ivanovich
Scapula, Jennyfer
Ghestem, Antoine
Carponcy, Julien
Libourel, Paul Antoine
Bras, Hélène
Abdelmeguid, Nabila ElSayed
Krook-Magnuson, Esther
Soltesz, Ivan
Bernard, Christophe
Luppi, Pierre-Hervé
Esclapez, Monique
author_facet Billwiller, Francesca
Castillo, Laura
Elseedy, Heba
Ivanov, Anton Ivanovich
Scapula, Jennyfer
Ghestem, Antoine
Carponcy, Julien
Libourel, Paul Antoine
Bras, Hélène
Abdelmeguid, Nabila ElSayed
Krook-Magnuson, Esther
Soltesz, Ivan
Bernard, Christophe
Luppi, Pierre-Hervé
Esclapez, Monique
author_sort Billwiller, Francesca
collection PubMed
description Several studies suggest that neurons from the lateral region of the SuM (SuML) innervating the dorsal dentate gyrus (DG) display a dual GABAergic and glutamatergic transmission and are specifically activated during paradoxical (REM) sleep (PS). The objective of the present study is to characterize the anatomical, neurochemical and electrophysiological properties of the SuML-DG projection neurons and to determine how they control DG oscillations and neuronal activation during PS and other vigilance states. For this purpose, we combine structural connectivity techniques using neurotropic viral vectors (rabies virus, AAV), neurochemical anatomy (immunohistochemistry, in situ hybridization) and imaging (light, electron and confocal microscopy) with in vitro (patch clamp) and in vivo (LFP, EEG) optogenetic and electrophysiological recordings performed in transgenic VGLUT2-cre male mice. At the cellular level, we show that the SuML-DG neurons co-release GABA and glutamate on dentate granule cells and increase the activity of a subset of DG granule cells. At the network level, we show that activation of the SuML-DG pathway increases theta power and frequency during PS as well as gamma power during PS and waking in the DG. At the behavioral level, we show that the activation of this pathway does not change animal behavior during PS, induces awakening during slow wave sleep and increases motor activity during waking. These results suggest that the SuML-DG pathway is capable of supporting the increase of theta and gamma power in the DG observed during PS and plays an important modulatory role of DG network activity during this state.
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spelling pubmed-76743722020-11-30 GABA–glutamate supramammillary neurons control theta and gamma oscillations in the dentate gyrus during paradoxical (REM) sleep Billwiller, Francesca Castillo, Laura Elseedy, Heba Ivanov, Anton Ivanovich Scapula, Jennyfer Ghestem, Antoine Carponcy, Julien Libourel, Paul Antoine Bras, Hélène Abdelmeguid, Nabila ElSayed Krook-Magnuson, Esther Soltesz, Ivan Bernard, Christophe Luppi, Pierre-Hervé Esclapez, Monique Brain Struct Funct Original Article Several studies suggest that neurons from the lateral region of the SuM (SuML) innervating the dorsal dentate gyrus (DG) display a dual GABAergic and glutamatergic transmission and are specifically activated during paradoxical (REM) sleep (PS). The objective of the present study is to characterize the anatomical, neurochemical and electrophysiological properties of the SuML-DG projection neurons and to determine how they control DG oscillations and neuronal activation during PS and other vigilance states. For this purpose, we combine structural connectivity techniques using neurotropic viral vectors (rabies virus, AAV), neurochemical anatomy (immunohistochemistry, in situ hybridization) and imaging (light, electron and confocal microscopy) with in vitro (patch clamp) and in vivo (LFP, EEG) optogenetic and electrophysiological recordings performed in transgenic VGLUT2-cre male mice. At the cellular level, we show that the SuML-DG neurons co-release GABA and glutamate on dentate granule cells and increase the activity of a subset of DG granule cells. At the network level, we show that activation of the SuML-DG pathway increases theta power and frequency during PS as well as gamma power during PS and waking in the DG. At the behavioral level, we show that the activation of this pathway does not change animal behavior during PS, induces awakening during slow wave sleep and increases motor activity during waking. These results suggest that the SuML-DG pathway is capable of supporting the increase of theta and gamma power in the DG observed during PS and plays an important modulatory role of DG network activity during this state. Springer Berlin Heidelberg 2020-09-24 2020 /pmc/articles/PMC7674372/ /pubmed/32970253 http://dx.doi.org/10.1007/s00429-020-02146-y Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Billwiller, Francesca
Castillo, Laura
Elseedy, Heba
Ivanov, Anton Ivanovich
Scapula, Jennyfer
Ghestem, Antoine
Carponcy, Julien
Libourel, Paul Antoine
Bras, Hélène
Abdelmeguid, Nabila ElSayed
Krook-Magnuson, Esther
Soltesz, Ivan
Bernard, Christophe
Luppi, Pierre-Hervé
Esclapez, Monique
GABA–glutamate supramammillary neurons control theta and gamma oscillations in the dentate gyrus during paradoxical (REM) sleep
title GABA–glutamate supramammillary neurons control theta and gamma oscillations in the dentate gyrus during paradoxical (REM) sleep
title_full GABA–glutamate supramammillary neurons control theta and gamma oscillations in the dentate gyrus during paradoxical (REM) sleep
title_fullStr GABA–glutamate supramammillary neurons control theta and gamma oscillations in the dentate gyrus during paradoxical (REM) sleep
title_full_unstemmed GABA–glutamate supramammillary neurons control theta and gamma oscillations in the dentate gyrus during paradoxical (REM) sleep
title_short GABA–glutamate supramammillary neurons control theta and gamma oscillations in the dentate gyrus during paradoxical (REM) sleep
title_sort gaba–glutamate supramammillary neurons control theta and gamma oscillations in the dentate gyrus during paradoxical (rem) sleep
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674372/
https://www.ncbi.nlm.nih.gov/pubmed/32970253
http://dx.doi.org/10.1007/s00429-020-02146-y
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