Caspase cleavage of tau: Linking amyloid and neurofibrillary tangles in Alzheimer's disease
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Abstract
The principal pathological features of Alzheimer's disease (AD) are extracellular amyloid plaques and intracellular neurofibrillary tangles, the latter composed of the microtubule-binding protein tau assembled into paired helical and straight filaments. Recent studies suggest that these pathological entities may be functionally linked, although the mechanisms by which amyloid deposition promotes pathological tau filament assembly are poorly understood. Here, we report that tau is proteolyzed by multiple caspases at a highly conserved aspartate residue (Asp421) in its C terminus in vitro and in neurons treated with amyloid-beta (Abeta) (1-42) peptide. Tau is rapidly cleaved at Asp421 in Abeta-treated neurons…
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14Topics & keywords
Topics
Keywords
- Tau protein
- Alzheimer's disease
- Proteolysis
- Chemistry
- Neurofibrillary tangle
- Senile plaques
- Biochemistry of Alzheimer's disease
- P3 peptide
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