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ADAM10 Plasma and CSF Levels Are Increased in Mild Alzheimer’s Disease

Authors :
Izabela Pereira Vatanabe
Rafaela Peron
Marina Mantellatto Grigoli
Silvia Pelucchi
Giulia De Cesare
Thamires Magalhães
Patricia Regina Manzine
Marcio Luiz Figueredo Balthazar
Monica Di Luca
Elena Marcello
Marcia Regina Cominetti
Source :
International Journal of Molecular Sciences, Vol 22, Iss 5, p 2416 (2021)
Publication Year :
2021
Publisher :
MDPI AG, 2021.

Abstract

ADAM10 is the main α-secretase that participates in the non-amyloidogenic cleavage of amyloid precursor protein (APP) in neurons, inhibiting the production of β-amyloid peptide (Aβ) in Alzheimer’s disease (AD). Strong recent evidence indicates the importance of the localization of ADAM10 for its activity as a protease. In this study, we investigated ADAM10 activity in plasma and CSF samples of patients with amnestic mild cognitive impairment (aMCI) and mild AD compared with cognitively healthy controls. Our results indicated that plasma levels of soluble ADAM10 were significantly increased in the mild AD group, and that in these samples the protease was inactive, as determined by activity assays. The same results were observed in CSF samples, indicating that the increased plasma ADAM10 levels reflect the levels found in the central nervous system. In SH-SY5Y neuroblastoma cells, ADAM10 achieves its major protease activity in the fraction obtained from plasma membrane lysis, where the mature form of the enzyme is detected, confirming the importance of ADAM10 localization for its activity. Taken together, our results demonstrate the potential of plasma ADAM10 to act as a biomarker for AD, highlighting its advantages as a less invasive, easier, faster, and lower-cost processing procedure, compared to existing biomarkers.

Details

Language :
English
ISSN :
14220067 and 16616596
Volume :
22
Issue :
5
Database :
Directory of Open Access Journals
Journal :
International Journal of Molecular Sciences
Publication Type :
Academic Journal
Accession number :
edsdoj.8552cce2af4a4f63a1061442f2c0422f
Document Type :
article
Full Text :
https://doi.org/10.3390/ijms22052416