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
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