Abeta oligomer-mediated long-term potentiation impairment involves protein phosphatase 1-dependent mechanisms.
Détails
Télécharger: Journal of Neuroscience 2007 Knobloch.pdf (424.23 [Ko])
Etat: Public
Version: Final published version
Etat: Public
Version: Final published version
ID Serval
serval:BIB_7CE3F0541502
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Abeta oligomer-mediated long-term potentiation impairment involves protein phosphatase 1-dependent mechanisms.
Périodique
The Journal of neuroscience
ISSN
1529-2401 (Electronic)
ISSN-L
0270-6474
Statut éditorial
Publié
Date de publication
18/07/2007
Peer-reviewed
Oui
Volume
27
Numéro
29
Pages
7648-7653
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Publication Status: ppublish
Résumé
Amyloid beta (Abeta) oligomers are derived from proteolytic cleavage of amyloid precursor protein (APP) and can impair memory and hippocampal long-term potentiation (LTP) in vivo and in vitro. They are recognized as the primary neurotoxic agents in Alzheimer's disease. The mechanisms underlying such toxicity on synaptic functions are complex and not fully understood. Here, we provide the first evidence that these mechanisms involve protein phosphatase 1 (PP1). Using a novel transgenic mouse model expressing human APP with the Swedish and Arctic mutations that render Abeta more prone to form oligomers (arcAbeta mice), we show that the LTP impairment induced by Abeta oligomers can be fully reversed by PP1 inhibition in vitro. We further demonstrate that the genetic inhibition of endogenous PP1 in vivo confers resistance to Abeta oligomer-mediated toxicity and preserves LTP. Overall, these results reveal that PP1 is a key player in the mechanisms of AD pathology.
Mots-clé
Age Factors, Amyloid Precursor Protein Secretases/genetics, Amyloid beta-Peptides/chemistry, Amyloid beta-Peptides/metabolism, Amyloid beta-Peptides/ultrastructure, Analysis of Variance, Animals, Calcium-Calmodulin-Dependent Protein Kinase Type 2, Calcium-Calmodulin-Dependent Protein Kinases/genetics, Dose-Response Relationship, Radiation, Electric Stimulation/methods, Excitatory Postsynaptic Potentials/drug effects, Excitatory Postsynaptic Potentials/physiology, Gene Expression Regulation/genetics, Hippocampus/cytology, Humans, In Vitro Techniques, Long-Term Potentiation/genetics, Long-Term Potentiation/physiology, Long-Term Potentiation/radiation effects, Mice, Mice, Transgenic, Microscopy, Electron, Transmission/methods, Neurons/drug effects, Neurons/physiology, Patch-Clamp Techniques, Phosphoprotein Phosphatases/physiology, Presenilin-1/genetics, Protein Phosphatase 1, Reverse Transcriptase Polymerase Chain Reaction/methods
Pubmed
Web of science
Open Access
Oui
Création de la notice
25/05/2018 8:45
Dernière modification de la notice
20/08/2019 14:38