Publication year
2015Source
Journal of Neurochemistry, 134, 6, (2015), pp. 1152-1162ISSN
Publication type
Article / Letter to editor

Display more detailsDisplay less details
Organization
Neurology
Laboratory Medicine
Pathology
Geriatrics
Journal title
Journal of Neurochemistry
Volume
vol. 134
Issue
iss. 6
Page start
p. 1152
Page end
p. 1162
Subject
Radboudumc 0: Other Research RIMLS: Radboud Institute for Molecular Life Sciences; Radboudumc 17: Women's cancers RIHS: Radboud Institute for Health Sciences; Radboudumc 1: Alzheimer`s disease DCMN: Donders Center for Medical Neuroscience; Radboudumc 3: Disorders of movement DCMN: Donders Center for Medical NeuroscienceAbstract
Amyloid-beta (Abeta) is the most prominent protein in Alzheimer's disease (AD) senile plaques. In addition, Abeta interacts with a variety of Abeta-associated proteins (AAPs), some of which can form complexes with Abeta and influence its clearance, aggregation or toxicity. Identification of novel AAPs may shed new light on the pathophysiology of AD and the metabolic fate of Abeta. In this study, we aimed to identify new AAPs by searching for proteins that may form soluble complexes with Abeta in CSF, using a proteomics approach. We identified the secreted Wnt pathway protein Dickkopf-related protein 3 (Dkk-3) as a potential Abeta-associated protein. Using immunohistochemistry on human AD brain tissue, we observed that (i) Dkk-3 co-localizes with Abeta in the brain, both in diffuse and classic plaques. (ii) Dkk-3 is expressed in neurons and in blood vessel walls in the brain and (iii) is secreted by leptomeningeal smooth muscle cells in vitro. Finally, measurements using ELISA revealed that (iv) Dkk-3 protein is abundantly present in both cerebrospinal fluid and serum, but its levels are similar in non-demented controls and patients with AD, Lewy body dementia, and frontotemporal dementia. Our study demonstrates that Dkk-3 is a hitherto unidentified Abeta-associated protein which, given its relatively high cerebral concentrations and co-localization with Abeta, is potentially involved in AD pathology. In this study, we propose that Dickkopf-related protein-3 (Dkk-3) might be a novel Amyloid-beta (Abeta) associated protein. We demonstrate that Dkk-3 is expressed in the brain, especially in vessel walls, and co-localizes with Abeta in senile plaques. Furthermore, Dkk-3 levels in cerebrospinal fluid strongly correlate with Abeta40 levels, but were not suitable to discriminate non-demented controls and patients with dementia.
This item appears in the following Collection(s)
- Academic publications [203608]
- Faculty of Medical Sciences [80231]
Upload full text
Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.