Astrocytic <scp>mGluR5</scp> Regulation of Synaptic Transmission is Activity‐Dependent in Adult Rats

Data accumulated over the last two decades have demonstrated that astrocytes play key roles in the regulation of synaptic transmission and plasticity. This is due, among other mechanisms, to their capability to detect and regulate synaptic transmission by expressing receptors and releasing gliotransmitters, respectively. Importantly, in juvenile rats, astrocytes are able to detect glutamate release at the level of individual synapses through mGluR5 and consequently up-regulate excitatory synaptic transmission efficacy through the release of purines. Whether this upregulation is still present in the adult brain is an open question. Using immunohistochemistry and RNAscope on fixed tissue, as well as electrophysiological recordings on acute hippocampal brain slices of adult male rats, we demonstrated that this regulatory pathway also prevails in adult rats. Most surprisingly, such facilitation of glutamate release that is readily observed when a small number of synapses are activated was completely abolished under conditions where a large number of inputs were stimulated. These findings thus suggest that astrocytes integrate the incoming afferent information and adapt their responses depending on the network activity.

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Publication Details

Journal
Glia
Published
2026-06-17
DOI
https://doi.org/10.1002/glia.70162
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Astrocytic mGluR5 Regulation of Synaptic Transmission is Activity‐Dependent in Adult Rats

Marjorie Varilh, Philippe Ciofi, Muna L. Hilal, Dorian Arnouil et al.
Glia
Neuroscience and Neuropharmacology Research
article

Astrocytic mGluR5 Regulation of Synaptic Transmission is Activity‐Dependent in Adult Rats

Marjorie Varilh, Philippe Ciofi, Muna L. Hilal, Dorian Arnouil, Charlène Joséphine, Dylan Pommier, Sarah Mountadem, Daniela Cota, Giovanni Marsicano, Astrid Cannich, Alexis‐Pierre Bemelmans, Julien Bourel, Vincent Simon, Stéphane H. R. Oliet, Valentin Langlais, Aude Panatier, Sébastien Marais, Aurélie Amadio, Marie Miegebielle
article en

Abstract

Data accumulated over the last two decades have demonstrated that astrocytes play key roles in the regulation of synaptic transmission and plasticity. This is due, among other mechanisms, to their capability to detect and regulate synaptic transmission by expressing receptors and releasing gliotransmitters, respectively. Importantly, in juvenile rats, astrocytes are able to detect glutamate release at the level of individual synapses through mGluR5 and consequently up-regulate excitatory synaptic transmission efficacy through the release of purines. Whether this upregulation is still present in the adult brain is an open question. Using immunohistochemistry and RNAscope on fixed tissue, as well as electrophysiological recordings on acute hippocampal brain slices of adult male rats, we demonstrated that this regulatory pathway also prevails in adult rats. Most surprisingly, such facilitation of glutamate release that is readily observed when a small number of synapses are activated was completely abolished under conditions where a large number of inputs were stimulated. These findings thus suggest that astrocytes integrate the incoming afferent information and adapt their responses depending on the network activity.

GliaVol. 74(8)
Centre National de la Recherche Scientifique (FR), Université de Bordeaux (FR), Inserm (FR), Commissariat à l'Énergie Atomique et aux Énergies Alternatives (FR), Université Paris-Saclay (FR), CEA Paris-Saclay - Etablissement de Fontenay-aux-roses (FR), Bordeaux Population Health (FR), Direction de la Recherche Fondamentale (FR), Neurocentre Magendie (FR)
Agence Nationale de la Recherche, Institut National de la Santé et de la Recherche Médicale, Fondation pour la Recherche Médicale, Ministère de l'Education Nationale, de l'Enseignement Superieur et de la Recherche, Centre National de la Recherche Scientifique
Openalex Percentile: Top 11%
Neuroscience and Neuropharmacology Research
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