Abstract |
Familial British dementia (FBD) is an autosomal dominant neurodegenerative disorder, with biochemical and pathological similarities to Alzheimer's disease. FBD is associated with a point mutation in the stop codon of the BRI gene. The mutation extends the length of the wild-type protein by 11 amino acids, and following proteolytic cleavage, results in the production of a cyclic peptide (ABri) 11 amino acids longer than the wild-type (WT) peptide produced from the normal gene BRI. ABri was found to be the main component of amyloid deposits in FBD brains. However, pathological examination of FBD brains has shown the presence of ABri as non-fibrillar deposits as well as amyloid fibrils. Taken together, the genetic, pathological and biochemical data support the hypothesis that ABri deposits play a central role in the pathogenesis of FBD. Here we report that ABri, but not WT peptide, can oligomerise and form amyloid-like fibrils. We show for the first time that ABri induces apoptotic cell death, whereas WT is not toxic to cells. Moreover, we report the novel findings that non-fibrillar oligomeric species of ABri are more toxic than protofibrils and mature fibrils. These findings provide evidence that non-fibrillar oligomeric species are likely to play a critical role in the pathogenesis of FBD and suggest that a similar process may also operate in other neurodegenerative diseases.
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Authors | O M El-Agnaf, S Nagala, B P Patel, B M Austen |
Journal | Journal of molecular biology
(J Mol Biol)
Vol. 310
Issue 1
Pg. 157-68
(Jun 29 2001)
ISSN: 0022-2836 [Print] Netherlands |
PMID | 11419943
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright 2001 Academic Press. |
Chemical References |
- Adaptor Proteins, Signal Transducing
- Amyloid
- Formazans
- ITM2B protein, human
- Membrane Glycoproteins
- Membrane Proteins
- Peptide Fragments
- Phosphatidylserines
- Tetrazolium Salts
- MTT formazan
- Congo Red
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Topics |
- Adaptor Proteins, Signal Transducing
- Amyloid
(chemistry, genetics, metabolism, ultrastructure)
- Apoptosis
- Birefringence
- Cell Line
- Cell Survival
- Chromatography, Gel
- Congo Red
- Dementia
(genetics, metabolism, pathology)
- England
- Formazans
- Humans
- Membrane Glycoproteins
- Membrane Proteins
- Microscopy, Electron
- Mutation
(genetics)
- Peptide Fragments
(chemistry, genetics, metabolism, ultrastructure)
- Phosphatidylserines
(metabolism)
- Protein Structure, Quaternary
- Tetrazolium Salts
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