mGluR5 as a Potential Orchestrator of Astrocyte Interactions in Neurological Disorders

Copyright © 2025 Jeongseop Kim et al. Neural Plasticity published by John Wiley & Sons Ltd.

Détails bibliographiques
Publié dans:Neural plasticity. - 1998. - 2025(2025) vom: 28., Seite 7259018
Auteur principal: Kim, Jeongseop (Auteur)
Autres auteurs: Lee, Jiyong, Song, Hyein, Koo, Ja Wook, Kang, Shinwoo
Format: Article en ligne
Langue:English
Publié: 2025
Accès à la collection:Neural plasticity
Sujets:Journal Article Review astrocyte mGluR5 neuroinflammation synaptic homeostasis therapeutic potential Receptor, Metabotropic Glutamate 5
Description
Résumé:Copyright © 2025 Jeongseop Kim et al. Neural Plasticity published by John Wiley & Sons Ltd.
Astrocytes and metabotropic glutamate receptor 5 (mGluR5) have emerged as pivotal regulators of synaptic homeostasis and neural communication within the central nervous system (CNS). Although mGluR5 has long been considered neuron-specific, its functional expression in astrocytes is now recognized as essential for calcium (Ca2+) signaling, gliotransmission, and the modulation of synaptic plasticity. Dysregulation of astrocytic mGluR5 is increasingly implicated in the pathophysiology of neurodegenerative and psychiatric disorders including Alzheimer's disease (AD), Parkinson's disease (PD), depression, anxiety, and schizophrenia (SCZ) by promoting neuroinflammation, excitotoxicity, and synaptic dysfunction. In this review, we explore the emerging role of astrocytic mGluR5 in mediating astrocyte-neuron communication and its maladaptive regulation in disease contexts. We also assess the therapeutic potential of targeting astrocytic mGluR5, highlighting advances in pharmacological modulators, gene therapy, and RNA-based strategies aimed at restoring homeostatic function. Despite recent progress, critical knowledge gaps remain, particularly regarding the regional specificity of astrocytic mGluR5 effects, its crosstalk with other signaling pathways, and its contribution to chronic neuroinflammation. Addressing these challenges may unlock innovative astrocyte-targeted therapies to restore synaptic integrity and protect against neurodegeneration in CNS disorders
Description:Date Completed 18.09.2025
Date Revised 20.09.2025
published: Electronic-eCollection
Citation Status MEDLINE
ISSN:1687-5443
DOI:10.1155/np/7259018