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The Role of Astrocytes in Synapse Loss in Alzheimer's Disease: A Systematic Review.

Authors :
Hulshof LA
van Nuijs D
Hol EM
Middeldorp J
Source :
Frontiers in cellular neuroscience [Front Cell Neurosci] 2022 Jun 16; Vol. 16, pp. 899251. Date of Electronic Publication: 2022 Jun 16 (Print Publication: 2022).
Publication Year :
2022

Abstract

Alzheimer's disease (AD) is the most common cause of dementia, affecting 35 million people worldwide. One pathological feature of progressing AD is the loss of synapses. This is the strongest correlate of cognitive decline. Astrocytes, as an essential part of the tripartite synapse, play a role in synapse formation, maintenance, and elimination. During AD, astrocytes get a reactive phenotype with an altered gene expression profile and changed function compared to healthy astrocytes. This process likely affects their interaction with synapses. This systematic review aims to provide an overview of the scientific literature including information on how astrocytes affect synapse formation and elimination in the brain of AD patients and in animal models of the disease. We review molecular and cellular changes in AD astrocytes and conclude that these predominantly result in lower synapse numbers, indicative of decreased synapse support or even synaptotoxicity, or increased elimination, resulting in synapse loss, and consequential cognitive decline, as associated with AD. Preventing AD induced changes in astrocytes might therefore be a potential therapeutic target for dementia. Systematic Review Registration: https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=148278, identifier [CRD148278].<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2022 Hulshof, van Nuijs, Hol and Middeldorp.)

Details

Language :
English
ISSN :
1662-5102
Volume :
16
Database :
MEDLINE
Journal :
Frontiers in cellular neuroscience
Accession number :
35783099
Full Text :
https://doi.org/10.3389/fncel.2022.899251