Abstract
Alzheimer's disease (AD) is the most common neurodegenerative disease in the world. The pathogenesis of AD is associated with beta-amyloid (Abeta) fibrillation. Nanoparticles have large surface area and can access the brain. But no investigation has been made to study the relationship between nanoparticles and AD. In our study, we observed Abeta fibril formation in the presence of six kinds of nanoparticles and found that TiO2 nanoparticles can promote Abeta fibrillation by shortening nucleation process, which is the key rate-determining step of fibrillation. Hereby the interaction between Abeta and nanoparticles may contribute to AD etiology.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Alzheimer Disease / etiology*
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Amyloid beta-Peptides / chemistry
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Amyloid beta-Peptides / metabolism*
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Amyloid beta-Peptides / ultrastructure
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Cerium / chemistry
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Environmental Exposure
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Fullerenes / chemistry
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Humans
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Microscopy, Electron, Transmission
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Nanoparticles / chemistry*
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Nanoparticles / toxicity
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Peptide Fragments / chemistry
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Peptide Fragments / metabolism
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Peptide Fragments / ultrastructure
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Silicon Dioxide / chemistry
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Titanium / chemistry*
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Titanium / toxicity
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Zirconium / chemistry
Substances
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Amyloid beta-Peptides
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Fullerenes
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Peptide Fragments
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amyloid beta-protein (1-42)
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fullerene C70
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titanium dioxide
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Cerium
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ceric oxide
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Silicon Dioxide
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Zirconium
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Titanium
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zirconium oxide