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• W2091240011 abstract "One of the pathological hallmarks of Alzheimer's disease (AD) is neurofibrillary tangles (NFTs), which are composed of abnormally hyperphosphorylated tau, but the mechanism of tau hyperphosphorylation in AD is still unclear. To investigate the effects of estrogens on tau phosphorylation, SH-SY5Y cells were treated with okadaic acid (OA), a serine/threonine phosphatase inhibitor, to induce tau phosphorylation and the effects of estrogen were observed by co-treatment with 17β-estradiol (E2). We found that OA induced in vitro tau hyperphosphorylation, which was prevented by E2 in a dose-dependent manner. This effect of E2 was partially blocked by an estrogen receptor (ER) antagonist, ICI 182,780. In addition to tau hyperphosphorylation, inhibition of serine/threonine phosphorylation induced upregulation of cdk5 levels, which was attenuated by E2 in a manner that was counteracted by ICI 182,780. Our results show that cdk5 is involved in OA-induced tau hyperphosphorylation, and estrogens ameliorate the tau hyperphosphorylation, which may be mediated in part by ER." @default.
• W2091240011 created "2016-06-24" @default.
• W2091240011 creator A5000051451 @default.
• W2091240011 creator A5024146315 @default.
• W2091240011 date "2010-07-01" @default.
• W2091240011 modified "2023-10-17" @default.
• W2091240011 title "Okadaic acid induces tau phosphorylation in SH-SY5Y cells in an estrogen-preventable manner" @default.
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• W2091240011 doi "https://doi.org/10.1016/j.brainres.2010.04.074" @default.
• W2091240011 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2913890" @default.
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