Journal
NEURODEGENERATIVE DISEASES
Volume 19, Issue 5-6, Pages 184-191Publisher
KARGER
DOI: 10.1159/000505851
Keywords
Alzheimer's disease; Exosomes; Pathological protein; Urine; Transmission electron microscopy; Nanoparticle tracking analysis
Categories
Funding
- National Natural Science Foundation of China [81671068, 81873727]
- Key Science and Technology Program of Henan Province, China [201701020]
Ask authors/readers for more resources
Background:Exosomes are nano-sized extracellular vesicles secreted by most cell types and abundantly present in body fluids, including blood, saliva, urine, cerebrospinal fluid, and breast milk. Exosomes can spread toxic amyloid-beta (A beta) and hyperphosphorylated tau between cells, contributing to neuronal loss in Alzheimer's disease (AD).Objective:To explore changes in the morphology, number, and pathological protein levels of urinary exosomes in AD patients compared with age-matched healthy subjects.Methods:In this study, enzyme-linked immunosorbent assay was used to detect the levels of A beta 1-42 and P-S396-tau (normalized by CD63) in urinary exosomes of AD patients and matched healthy subjects. We used transmission electron microscopy and nanoparticle tracking analysis to observe the exosomes.Results:We found that the levels of A beta 1-42 and P-S396-tau in the urinary exosomes of AD patients were higher than those of matched healthy controls. Exosomes taken from AD patients were more numerous.Conclusion:The differences in levels of A beta 1-42 and P-S396-tau and the quantity of urinary exosomes between AD patients and healthy controls may provide a basis for early diagnosis of AD.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available