Synapse pathology in Alzheimer's disease.
Alzheimer’s disease
Aβ
Microscopy
Synapse
Synaptome
Tau
Journal
Seminars in cell & developmental biology
ISSN: 1096-3634
Titre abrégé: Semin Cell Dev Biol
Pays: England
ID NLM: 9607332
Informations de publication
Date de publication:
04 2023
04 2023
Historique:
received:
10
03
2022
revised:
12
05
2022
accepted:
27
05
2022
pubmed:
12
6
2022
medline:
31
12
2022
entrez:
11
6
2022
Statut:
ppublish
Résumé
Synapse loss and damage are central features of Alzheimer's disease (AD) and contribute to the onset and progression of its behavioural and physiological features. Here we review the literature describing synapse pathology in AD, from what we have learned from microscopy in terms of its impacts on synapse architecture, to the mechanistic role of Aβ, tau and glial cells, mitochondrial dysfunction, and the link with AD risk genes. We consider the emerging view that synapse pathology may operate at a further level, that of synapse diversity, and discuss the prospects for leveraging new synaptome mapping methods to comprehensively understand the molecular properties of vulnerable and resilient synapses. Uncovering AD impacts on brain synapse diversity should inform therapeutic approaches targeted at preserving or replenishing lost and damaged synapses and aid the interpretation of clinical imaging approaches that aim to measure synapse damage.
Identifiants
pubmed: 35690535
pii: S1084-9521(22)00186-0
doi: 10.1016/j.semcdb.2022.05.028
pii:
doi:
Types de publication
Journal Article
Review
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
13-23Subventions
Organisme : Medical Research Council
Pays : United Kingdom
Informations de copyright
Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.
Déclaration de conflit d'intérêts
Conflict of Interest We declare there is no conflict of interest in the preparation of submission of this manuscript.