脱磷
τ蛋白
磷酸化
化学
细胞内
Tau病理学
陶氏病
阿尔茨海默病
淀粉样蛋白(真菌学)
细胞生物学
生物化学
生物物理学
分子生物学
生物
神经退行性变
内科学
磷酸酶
疾病
医学
无机化学
作者
Ruozhen Wu,Longfei Li,Ruirui Shi,Yan Zhou,Nana Jin,Jianlan Gu,Yunn Chyn Tung,Fei Liu,Dandan Chu
标识
DOI:10.3389/fnmol.2021.631833
摘要
Accumulation of intracellular neurofibrillary tangles (NFTs), which are constituted of abnormally phosphorylated tau, is one of the neuropathological hallmarks of Alzheimer’s disease (AD). The oligomeric aggregates of tau in AD brain (AD O-tau) are believed to trigger NFT spreading by seeding normal tau aggregation as toxic seeds, in a prion-like fashion. Here, we revealed the features of AD O-tau by Western blots using antibodies against various epitopes and determined the effect of dephosphorylation on the seeding activity of AD O-tau by capture and seeded aggregation assays. We found that N-terminal truncated and C-terminalhyperphosphorylated tau species were enriched in AD O-tau. Dephosphorylation of AD O-tau by alkaline phosphatasediminished its activity in capturing tau in vitro and ininducing insoluble aggregates in cultured cells. Our resultssuggested that dephosphorylation passivated the seeding activity ofAD O-tau. Inhibition of phosphorylation may be a potentstrategy to prevent the spreading of tau patho3logy.
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