Extracellular vesicle proteome unveils cathepsin B connection to Alzheimer’s disease pathogenesis

Author:

Yuyama Kohei1,Sun Hui1,Fujii Risa2,Hemmi Isao3,Ueda Koji2,Igeta Yukifusa45ORCID

Affiliation:

1. Lipid Biofunction Section, Faculty of Advanced Life Science, Hokkaido University , Sapporo 001-0021 , Japan

2. Cancer Proteomics Group, Cancer Precision Medicine Center, Japanese Foundation for Cancer Research , Tokyo 035-8550 , Japan

3. Department of Nursing, Japanese Red Cross College of Nursing , Tokyo 150-0012 , Japan

4. Department of Dementia, Dementia Center, Toranomon Hospital , Tokyo 105-8470 , Japan

5. Division of Dementia Research, Okinaka Memorial Institute for Medical Research , Tokyo 105-8470 , Japan

Abstract

Abstract Extracellular vesicles (EVs) are membrane vesicles that are released extracellularly and considered to be implicated in the pathogenesis of neurodegenerative diseases including Alzheimer’s disease. Here, CSF EVs of 16 ATN-classified cases were subjected to quantitative proteome analysis. In these CSF EVs, levels of 11 proteins were significantly altered during the ATN stage transitions (P < 0.05 and fold-change > 2.0). These proteins were thought to be associated with Alzheimer’s disease pathogenesis and represent candidate biomarkers for pathogenic stage classification. Enzyme-linked immunosorbent assay analysis of CSF and plasma EVs revealed altered levels of cathepsin B (CatB) during the ATN transition (seven ATN groups in validation set, n = 136). The CSF and plasma EV CatB levels showed a negative correlation with CSF amyloid-β42 concentrations. This proteomic landscape of CSF EVs in ATN classifications can depict the molecular framework of Alzheimer’s disease progression, and CatB may be considered a promising candidate biomarker and therapeutic target in Alzheimer’s disease amyloid pathology.

Funder

KAKENHI

Japan Society for the Promotion of Science

Okinaka Memorial Foundation

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

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