Different tau fibril types reduce prion level in chronically and de novo infected cells.
PrP(C)
PrP(Sc)
aggregation
conformers
neurodegeneration
prion diseases
prions
tau
tau fibrils
tauopathy
Journal
The Journal of biological chemistry
ISSN: 1083-351X
Titre abrégé: J Biol Chem
Pays: United States
ID NLM: 2985121R
Informations de publication
Date de publication:
08 2023
08 2023
Historique:
received:
16
01
2023
revised:
06
07
2023
accepted:
09
07
2023
medline:
31
8
2023
pubmed:
17
7
2023
entrez:
16
7
2023
Statut:
ppublish
Résumé
Neurodegenerative diseases are often characterized by the codeposition of different amyloidogenic proteins, normally defining distinct proteinopathies. An example is represented by prion diseases, where the classical deposition of the aberrant conformational isoform of the prion protein (PrP
Identifiants
pubmed: 37454740
pii: S0021-9258(23)02082-3
doi: 10.1016/j.jbc.2023.105054
pmc: PMC10432985
pii:
doi:
Substances chimiques
Amyloidogenic Proteins
0
Prion Proteins
0
Prions
0
tau Proteins
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
105054Informations de copyright
Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Conflict of interest The authors declare that they have no conflicts of interest with the contents of this article.