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Expression of BRI2 mRNA and protein in normal human brain and familial British dementia: its relevance to the pathogenesis of disease.

Authors :
Lashley T
Revesz T
Plant G
Bandopadhyay R
Lees AJ
Frangione B
Wood NW
de Silva R
Ghiso J
Rostagno A
Holton JL
Source :
Neuropathology and applied neurobiology [Neuropathol Appl Neurobiol] 2008 Oct; Vol. 34 (5), pp. 492-505. Date of Electronic Publication: 2008 Feb 13.
Publication Year :
2008

Abstract

Introduction: Two different disease-specific mutations in the BRI2 gene, situated on chromosome 13, have been identified as giving rise to familial British dementia (FBD) and familial Danish dementia (FDD). Each mutation results in extension of the open reading frame generating the disease-specific precursor proteins which are cleaved by furin-like proteolysis releasing the amyloidogenic C-terminal peptides ABri and ADan in FBD and FDD, respectively.<br />Material and Methods: To understand the mechanism of the formation of amyloid lesions in FBD, we studied the origin of the precursor proteins and furin in the human brain. We used control brains, cases of sporadic Alzheimer's disease (AD), variant AD with cotton wool plaques and FBD to study BRI2 mRNA expression using in situ hybridization. Furin and BRI2 protein expression was investigated using Western blotting and immunohistochemistry.<br />Results: BRI2 mRNA and BRI2 protein are widely expressed primarily by neurones and glia and are deposited in the amyloid lesions in FBD. They were, however, not expressed by cerebrovascular components. Furin expression showed a similar pattern except that it was also present in cerebrovascular smooth muscle cells.<br />Conclusions: These findings suggest that neurones and glia and are a major source of BRI2 protein and that in FBD, the mutated precursor protein may undergo furin cleavage within neurones to produce the amyloid peptide ABri. The failure to demonstrate BRI2 in blood vessels under the conditions tested suggests that vascular amyloid peptide production does not contribute significantly to cerebral amyloid angiopathy (CAA) in FBD and FDD, lending indirect support to the drainage hypothesis of CAA.

Details

Language :
English
ISSN :
1365-2990
Volume :
34
Issue :
5
Database :
MEDLINE
Journal :
Neuropathology and applied neurobiology
Publication Type :
Academic Journal
Accession number :
18282158
Full Text :
https://doi.org/10.1111/j.1365-2990.2008.00935.x