Fulltext:
58034.pdf
Embargo:
until further notice
Size:
972.0Kb
Format:
PDF
Description:
Publisher’s version
Publication year
2004Source
Neurobiology of Aging, 25, 1, (2004), pp. 93-103ISSN
Publication type
Article / Letter to editor
Display more detailsDisplay less details
Organization
Neurology
Pathology
Chemical Endocrinology
Journal title
Neurobiology of Aging
Volume
vol. 25
Issue
iss. 1
Page start
p. 93
Page end
p. 103
Subject
UMCN 1.3: Tumor microenvironment; UMCN 3.2: Cognitive neurosciences; UMCN 5.1: Genetic defects of metabolism; UMCN 5.2: Endocrinology and reproductionAbstract
Amyloid-beta (Abeta) deposition in the cerebral arterial and capillary walls is one of the characteristics of Alzheimer's disease and hereditary cerebral hemorrhage with amyloidosis-Dutch type. In vitro, Abeta1-40, carrying the "Dutch" mutation (DAbeta1-40), induced reproducible degeneration of cultured human brain pericytes (HBP), by forming fibrils at the cell surface. Thus, this culture system provides an useful model to study the vascular pathology seen in Alzheimer's disease. In this study, we used this model to investigate the effects of insulin on Abeta-induced degeneration of HBP, as it has been mentioned previously that insulin is able to protect neurons against Abeta-induced cell-death. The toxic effect of DAbeta1-40 on HBP was inhibited by insulin in a dose-dependent matter. Insulin interacted with Abeta and inhibited fibril formation of Abeta in a cell-free assay, as well as at the cell surface of HBP. Our data indicate that the formation of a fibril network is essential for Abeta-induced cell death in HBP. Additionally, insulin may be involved in the regulation of Abeta fibrillization in AD.
This item appears in the following Collection(s)
- Academic publications [244262]
- Electronic publications [131202]
- Faculty of Medical Sciences [92892]
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.