Modulation of phosphorylation of neuronal cytoskeletal proteins by neuronal depolarization.

Détails

ID Serval
serval:BIB_3ECC051D4CE7
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Modulation of phosphorylation of neuronal cytoskeletal proteins by neuronal depolarization.
Périodique
Cellular and Molecular Neurobiology
Auteur⸱e⸱s
Mata M., Honegger P., Fink D.J.
ISSN
0272-4340 (Print)
ISSN-L
0272-4340
Statut éditorial
Publié
Date de publication
1997
Volume
17
Numéro
1
Pages
129-140
Langue
anglais
Résumé
1. The neuronal cytoskeletal protein tau and the carboxy tails of cytoskeletal proteins neurofilament-M (NF-M) and neurofilament-H (NF-H) are phosphorylated on serine residues by the cyclin-dependent kinase cdk-5. 2. In aggregating neuronal-glial cultures we show that veratridine-mediated cation influx causes dephosphorylation of tau, NF-M and NF-H. Dephosphorylation was blocked specifically by cyclosporine A but not by okadiac acid at concentrations up to 200 nM. 3. These results suggest that veratridine-triggered cation influx causes activation of PP-2B (calcineurin) leading to dephosphorylation of these cytoskeletal proteins.
Mots-clé
Animals, Blotting, Western, Cells, Cultured, Cytoskeletal Proteins/drug effects, Cytoskeletal Proteins/metabolism, Embryo, Mammalian, Nerve Tissue Proteins/drug effects, Nerve Tissue Proteins/metabolism, Neurofilament Proteins/drug effects, Neurofilament Proteins/metabolism, Neuromuscular Depolarizing Agents/pharmacology, Phosphoric Monoester Hydrolases/drug effects, Phosphoric Monoester Hydrolases/physiology, Phosphorylation/drug effects, Rats, Sodium/metabolism, Veratridine/pharmacology, tau Proteins/metabolism
Pubmed
Web of science
Création de la notice
24/01/2008 13:11
Dernière modification de la notice
20/08/2019 13:35
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