Caspase-6 activity predicts lower episodic memory ability in aged individuals |
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Authors: | Jasmine Ramcharitar Veronica M. Afonso Steffen Albrecht David A. Bennett Andrea C. LeBlanc |
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Affiliation: | 1. Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada;2. The Bloomfield Center for Research in Aging, Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Quebec, Canada;3. Department of Pathology, McGill University, Montreal, Quebec, Canada;4. Rush Alzheimer''s Disease Center, Rush University Medical Center, Chicago, Illinois, USA;5. Department of Neurological Sciences, Rush University Medical Center, Chicago, Illinois, USA |
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Abstract: | Caspase-6 (Casp6), a cysteinyl protease that induces axonal degeneration, is activated early in Alzheimer Disease (AD) brains. To determine whether Casp6 activation is responsible for early cognitive impairment, we investigated the abundance of Casp6 activity, paired helical filament–1 (PHF-1) phosphorylated Tau and amyloid beta peptide (Aβ) pathology by immunohistochemistry in the hippocampal formation of aged non–cognitively impaired (NCI) individuals. Casp6 activity was restricted to the entorhinal cortex (ERC) and CA1 regions of the hippocampus. Pathology scores were then correlated with cognitive scores obtained within 1 year of death. Regression analyses revealed that ERC and CA1 Casp6 activity were the main contributor to lower episodic memory performance, whereas ERC PHF-1 pathology predicted lower semantic and working memory performance. Aβ did not correlate with any of the cognitive tests. Because Casp6 activity and PHF-1 pathology are intimately associated with AD pathology and memory decline is an early event in AD, we conclude that Casp6 activity and PHF-1 immunoreactivity in ERC identifies aged individuals at risk for developing AD. |
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Keywords: | Caspase-6 Alzheimer disease Memory performance Aged individuals and cognition Episodic memory Working memory Semantic memory Visuospatial abilities Perceptual speed |
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