Glycogen Synthase Kinase 3: Ion Channels, Plasticity, and Diseases.

GSK3β-mediated phosphorylation intracellular fibroblast growth factors (iFGF) neuronal excitability neuronal plasticity neuropsychiatric disorders protein–protein interaction sodium- and potassium-current voltage-gated ion channels

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
16 Apr 2022
Historique:
received: 28 02 2022
revised: 13 04 2022
accepted: 14 04 2022
entrez: 23 4 2022
pubmed: 24 4 2022
medline: 27 4 2022
Statut: epublish

Résumé

Glycogen synthase kinase 3β (GSK3) is a multifaceted serine/threonine (S/T) kinase expressed in all eukaryotic cells. GSK3β is highly enriched in neurons in the central nervous system where it acts as a central hub for intracellular signaling downstream of receptors critical for neuronal function. Unlike other kinases, GSK3β is constitutively active, and its modulation mainly involves inhibition via upstream regulatory pathways rather than increased activation. Through an intricate converging signaling system, a fine-tuned balance of active and inactive GSK3β acts as a central point for the phosphorylation of numerous primed and unprimed substrates. Although the full range of molecular targets is still unknown, recent results show that voltage-gated ion channels are among the downstream targets of GSK3β. Here, we discuss the direct and indirect mechanisms by which GSK3β phosphorylates voltage-gated Na

Identifiants

pubmed: 35457230
pii: ijms23084413
doi: 10.3390/ijms23084413
pmc: PMC9028019
pii:
doi:

Substances chimiques

Ion Channels 0
Glycogen Synthase Kinase 3 beta EC 2.7.11.1
Protein Serine-Threonine Kinases EC 2.7.11.1
Glycogen Synthase Kinase 3 EC 2.7.11.26

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIH HHS
ID : R01ES031823/NH/NIH HHS/United States
Pays : United States
Organisme : NIEHS NIH HHS
ID : P30 ES030285
Pays : United States
Organisme : NIH HHS
ID : NIH/NIMH R01MH124351/NH/NIH HHS/United States
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH124351
Pays : United States
Organisme : NIEHS NIH HHS
ID : R01 ES031823
Pays : United States

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Auteurs

Mate Marosi (M)

Department of Pharmacology & Toxicology, University of Texas Medical Branch, Galveston, TX 77555, USA.

Parsa Arman (P)

Department of Pharmacology & Toxicology, University of Texas Medical Branch, Galveston, TX 77555, USA.

Giuseppe Aceto (G)

Department of Neuroscience, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
Fondazione Policlinico Universitario A. Gemelli, Istituto di Ricovero e Cura a Carattere Scientifico, 00168 Roma, Italy.

Marcello D'Ascenzo (M)

Department of Neuroscience, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
Fondazione Policlinico Universitario A. Gemelli, Istituto di Ricovero e Cura a Carattere Scientifico, 00168 Roma, Italy.

Fernanda Laezza (F)

Department of Pharmacology & Toxicology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Center for Addiction Research, Center for Biomedical Engineering, Mitchell Center for Neurodegenerative Diseases, Department of Pharmacology & Toxicology, 301 University Boulevard, Galveston, TX 77555, USA.

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Classifications MeSH