Published in:
01-08-2005 | Regular Paper
Caspase-cleaved tau accumulation in neurodegenerative diseases associated with tau and α-synuclein pathology
Authors:
Jodie Newman, Robert A. Rissman, Floyd Sarsoza, Ronald C. Kim, Malcolm Dick, David A. Bennett, Carl W. Cotman, Troy T. Rohn, Elizabeth Head
Published in:
Acta Neuropathologica
|
Issue 2/2005
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Abstract
Alzheimer’s disease (AD), Pick’s disease (PiD), progressive supranuclear palsy (PSP), corticobasal degeneration (CBD) and dementia with Lewy bodies (DLB) are diseases associated with the accumulation of tau or α-synuclein. In AD, β-amyloid (Aβ)-associated caspase activation and cleavage of tau at Asp421 (ΔTau) may be an early step in neurofibrillary tangle (NFT) formation. To examine whether ΔTau accumulates in other diseases not characterized by extracellular Aβ accumulation, we examined PiD, PSP, and CBD cases in comparison to those without extensive tau accumulation including frontotemporal lobar degeneration without Pick bodies (FTLD) and control cases. Additionally, we studied ΔTau accumulation in DLB cases associated with intracellular α-synuclein. ΔTau was observed in all disease cases except non-PiD FTLD and controls. These results demonstrate that the accumulation of ΔTau may represent a common pathway associated with abnormal accumulation of intracellular tau or α-synuclein and may be relatively less dependent on the extracellular accumulation of Aβ in non-AD dementias.