Dense core vesicle markers in CSF and cortical tissues of patients with Alzheimer's disease

New fluid biomarkers for Alzheimer's disease (AD) that reveal synaptic and neural network dysfunctions are needed for clinical practice and therapeutic trial design. Dense core vesicle (DCV) cargos are promising cerebrospinal fluid (CSF) indicators of synaptic failure in AD patients. However, t...

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Detalles Bibliográficos
Autores: Barranco, Neus|||0000-0002-6488-0815, Plá, Virginia|||0000-0002-5501-0789, Alcolea, Daniel|||0000-0002-3819-3245, Sánchez-Domínguez, Irene|||0000-0001-6421-8293, Fischer-Colbrie, Reiner, Ferrer, Isidro|||0000-0001-9888-8754, Lleó, Alberto|||0000-0002-2568-5478, Aguado, Fernando|||0000-0002-0393-1308
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:249789
Acceso en línea:https://ddd.uab.cat/record/249789
https://dx.doi.org/urn:doi:10.1186/s40035-021-00263-0
Access Level:acceso abierto
Palabra clave:Alzheimer's disease
Biomarkers
Cerebral cortex
Cerebrospinal fluid
Granulovacuolar degeneration
PCSK1
PCSK2
Tau protein
Descripción
Sumario:New fluid biomarkers for Alzheimer's disease (AD) that reveal synaptic and neural network dysfunctions are needed for clinical practice and therapeutic trial design. Dense core vesicle (DCV) cargos are promising cerebrospinal fluid (CSF) indicators of synaptic failure in AD patients. However, their value as biomarkers has not yet been determined. Immunoassays were performed to analyze the secretory proteins prohormone convertases PC1/3 and PC2, carboxypeptidase E (CPE), secretogranins SgIII and SgII, and Cystatin C in the cerebral cortex (n = 45, provided by Bellvitge University Hospital) and CSF samples (n = 66, provided by The Sant Pau Initiative on Neurodegeneration cohort) from AD patients (n = 56) and age-matched controls (n = 55). In AD tissues, most DCV proteins were aberrantly accumulated in dystrophic neurites and activated astrocytes, whereas PC1/3, PC2 and CPE were also specifically accumulated in hippocampal granulovacuolar degeneration bodies. AD individuals displayed an overall decline of secretory proteins in the CSF. Interestingly, in AD patients, the CSF levels of prohormone convertases strongly correlated inversely with those of neurodegeneration markers and directly with cognitive impairment status. These results demonstrate marked alterations of neuronal-specific prohormone convertases in CSF and cortical tissues of AD patients. The neuronal DCV cargos are biomarker candidates for synaptic dysfunction and neurodegeneration in AD. The online version contains supplementary material available at 10.1186/s40035-021-00263-0.