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Targetting Exosomes as a New Biomarker and Therapeutic Approach for Alzheimer's Disease
Stockholm University, Faculty of Social Sciences, Stress Research Institute.
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Number of Authors: 72020 (English)In: Clinical Interventions in Aging, ISSN 1176-9092, E-ISSN 1178-1998, Vol. 15, p. 195-205Article, review/survey (Refereed) Published
Abstract [en]

Alzheimer's disease (AD) is a neurodegenerative disease that mainly occurs in old age and involves progressive cognitive impairment. AD has become a major global issue for public health, with approximately 24 million people currently affected by the disease. Estimates indicted that this number will quadruple by 2050. Because of the high incidence of AD, there is an urgent need to develop new strategies to diagnose and treat AD. Many recent studies have indicated the multiple, yet somewhat controversial, roles of exosomes in AD. Although the underlying mechanisms by which exosomes play a role in AD are still unknown, current evidence suggests that exosomes can carry and spread toxic amyloid-beta, and hyperphosphorylated tau, between cells, and then induce apoptosis, thus contributing to the loss of neurons. In addition, exosomes appear to possess the ability to reduce brain amyloid-beta, and tau hyperphosphorylation, and transfer neuroprotective substances between neural cells. The accumulating data brings hope that the application of exosomes may be helpful for early diagnostics and the identification of new therapeutic targets for AD. Here, we summarized the various roles of exosomes, and how they might relate to the pathogenesis of AD. We also highlight the potential application of exosomes as a therapeutic option in AD therapy.

Place, publisher, year, edition, pages
2020. Vol. 15, p. 195-205
Keywords [en]
exosomes, alzheimer's disease, biomarker, mesenchymal stem cells, therapeutic strategy
National Category
Neurosciences Psychology
Research subject
Psychology
Identifiers
URN: urn:nbn:se:su:diva-181391DOI: 10.2147/CIA.S240400ISI: 000519926100001PubMedID: 32103922OAI: oai:DiVA.org:su-181391DiVA, id: diva2:1428745
Available from: 2020-05-06 Created: 2020-05-06 Last updated: 2022-03-23Bibliographically approved

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Pei, Jin-Jing

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