Hyperphosphorylation of Tau at Ser396 occurs in the much earlier stage than appearance of learning and memory disorders in 5XFAD mice
Abstract
The present study investigated the relation of age-dependent spatial learning/memory impairment and Tau phosphorylation in 5XFAD mice, a model of Alzheimer's disease. In the water maze test, the acquisition and retention latencies for 5XFAD mice at 6 months, but not 2 months, of age was significantly longer than those for wild-type mice at the same months of age, without difference in the swim speed and visual acuity between two groups. The level of glycogen synthase kinase 3β (GSK-3β) phosphorylation at Ser9 in the hippocampus for the 5XFAD mice at >4 months of age was significantly lesser than that for wild-type mice at the same months of age, while a robust increase in the Tyr216 phosphorylation of GSK-3β was found both in wild-type and 5XFAD mice at 6 months of age, without no significant difference in the extent between two groups. There was no significant difference in the Tau phosphorylation at Ser202/Thr205 in the hippocampus between two groups, but Ser396 phosphorylation for 5XFAD mice was significantly higher than that for wild-type mice at ages ranging from 2 to 6 months. The results of the present study indicate that Tau hyperphosphorylation in the brain for 5XFAD mice precedes high activation of GSK-3β and occurs in the much earlier stage than appearance of learning and memory disorders.
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The increase in hyperphosphorylated tau is likely indicative of neuronal debilitation that has culminated from the accumulation of neurotoxic Aβ.
“This increase in hyperphosphorylated tau is likely indicative of neuronal debilitation (Gendron and Petrucelli, 2009; Kanno et al., 2014) that has culminated from the accumulation of neurotoxic Aβ.”
From SYK coordinates neuroprotective microglial responses in neurodegenerative disease (2022) · cites this paper as Kanno et al., 2014
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References 14 · Cited by 76
- Authors
- Kanno, T., Tsuchiya, A., & Nishizaki, T.
- Affiliations
- Hyogo Medical University (JP)
- Corresponding author
- Nishizaki, Tomoyuki
- Venue
- Behavioural Brain Research
- Publisher
- Elsevier BV
- Published
- 2014-11
- Volume
- 274
- Pages
- 302-306
- ISSN
- 0166-4328 (ISSN-L)
- OpenAlex
- W1993327095
- Cited by
- 76
- References
- 14
- Citations by year
- 2026: 5 · 2025: 8 · 2024: 13 · 2023: 4 · 2022: 12 · 2021: 1 · 2020: 6 · 2019: 3 · 2018: 8 · 2017: 6 · 2016: 4 · 2015: 4 · 2014: 2
- FWCI
- 3.55
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Behavioural Brain Research (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- tau hyperphosphorylation, 5xFAD mice, Alzheimer's disease model, spatial learning and memory impairment, glycogen synthase kinase-3β, hippocampus, water maze
- MeSH terms
- Alzheimer Disease, Animals, Disease Models, Animal, Gene Expression Regulation, Learning Disabilities, Memory Disorders, Mice, Transgenic, Phosphorylation, Reaction Time, Serine, Swimming, Amyloid beta-Protein Precursor, tau Proteins, Maze Learning, Glycogen Synthase Kinase 3, Mice, Presenilin-1
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