GSK-3β orchestrates the inhibitory innervation of adult-born dentate granule cells in vivo.

Détails

ID Serval
serval:BIB_A6C271704373
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
GSK-3β orchestrates the inhibitory innervation of adult-born dentate granule cells in vivo.
Périodique
Cellular and molecular life sciences
Auteur⸱e⸱s
Moreno-Jiménez E.P., Flor-García M., Hernández-Vivanco A., Terreros-Roncal J., Rodríguez-Moreno C.B., Toni N., Méndez P., Llorens-Martín M.
ISSN
1420-9071 (Electronic)
ISSN-L
1420-682X
Statut éditorial
Publié
Date de publication
23/07/2023
Peer-reviewed
Oui
Volume
80
Numéro
8
Pages
225
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: epublish
Résumé
Adult hippocampal neurogenesis enhances brain plasticity and contributes to the cognitive reserve during aging. Adult hippocampal neurogenesis is impaired in neurological disorders, yet the molecular mechanisms regulating the maturation and synaptic integration of new neurons have not been fully elucidated. GABA is a master regulator of adult and developmental neurogenesis. Here we engineered a novel retrovirus encoding the fusion protein Gephyrin:GFP to longitudinally study the formation and maturation of inhibitory synapses during adult hippocampal neurogenesis in vivo. Our data reveal the early assembly of inhibitory postsynaptic densities at 1 week of cell age. Glycogen synthase kinase 3 Beta (GSK-3β) emerges as a key regulator of inhibitory synapse formation and maturation during adult hippocampal neurogenesis. GSK-3β-overexpressing newborn neurons show an increased number and altered size of Gephyrin <sup>+</sup> postsynaptic clusters, enhanced miniature inhibitory postsynaptic currents, shorter and distanced axon initial segments, reduced synaptic output at the CA3 and CA2 hippocampal regions, and impaired pattern separation. Moreover, GSK-3β overexpression triggers a depletion of Parvalbumin <sup>+</sup> interneuron perineuronal nets. These alterations might be relevant in the context of neurological diseases in which the activity of GSK-3β is dysregulated.
Mots-clé
Humans, Infant, Newborn, Brain/metabolism, Glycogen Synthase Kinase 3 beta/genetics, Glycogen Synthase Kinase 3 beta/metabolism, Hippocampus/metabolism, Neurogenesis, Neurons/metabolism, Adult, Adult hippocampal neurogenesis, Alzheimer´s disease, Behavior, Electrophysiology, GSK-3β, Gephyrin, Retrovirus
Pubmed
Web of science
Open Access
Oui
Création de la notice
31/07/2023 13:37
Dernière modification de la notice
19/12/2023 8:15
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