Cited by 31Alzheimer's disease research and treatmentsDementia and Cognitive Impairment ResearchNeuroinflammation and Neurodegeneration Mechanisms

Levels of tau phosphorylation at different sites in Alzheimer disease brain

Ikura, Yasumitsu, Kudo, Takashi, Tanaka, Toshihisa, Tanii, Hisashi, Grundke-Iqbal, Inge, Iqbal, Khalid, Takeda, Masatoshi·1998·NeuroReport

Abstract

The microtubule-associated protein tau is abnormally hyperphosphorylated in Alzheimer's disease (AD) brain. To date, 21 phosphorylated sites of tau have been identified. In the present study the levels of phosphorylation at Ser199/Ser202, Thr231/Ser235, Ser262/Ser356 and Ser396/Ser404 of tau in AD brain homogenate and its 100,000 x g supernatant were determined using radioimmuno-dot-blot assay. In homogenate, Ser199/Ser202 and Ser262/Ser356 were phosphorylated to similar level and were more phosphorylated than Thr231 or Ser396/Ser404. In supernatant, there was no significant difference in phosphorylated tau level among the investigated sites except for Thr231/Ser235 which was least phosphorylated. These results suggest that Ser199/Ser202 and Ser262/Ser356 are major sites of phosphorylation of tau in AD brain.

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Crossref · 10.1097/00001756-199807130-00041

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Authors
Ikura, Y., Kudo, T., Tanaka, T., Tanii, H., Grundke-Iqbal, I., Iqbal, K., & Takeda, M.
Affiliations
  • Osaka University Hospital (JP)
  • The University of Osaka (JP)
Venue
NeuroReport
Published
1998-07
Volume
9
Issue
10
Pages
2375-2379
ISSN
0959-4965 (ISSN-L)
OpenAlex
W2065525116
Cited by
31
References
0
Citations by year
2026: 2 · 2025: 3 · 2022: 1 · 2021: 1 · 2020: 3 · 2019: 1 · 2017: 1 · 2015: 1 · 2012: 2
FWCI
1.27
Type
journal article
Language
en
Open access
closed
Locations
  • Neuroreport (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 protein, tau phosphorylation, Alzheimer's disease, phosphorylation sites, microtubule-associated proteins, brain homogenate, subcellular fractionation
MeSH terms
Aged, Alzheimer Disease, Amino Acid Sequence, Brain, Brain Chemistry, Female, Humans, Male, Molecular Sequence Data, Phosphorylation, Radioimmunoassay, Temporal Lobe, tau Proteins

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