Manassero Giusi, Guglielmotto Michela, Monteleone Debora, Vasciaveo Valeria, Butenko Olena, Tamagno Elena, Arancio Ottavio, Tabaton Massimo
Neuroscience Institute of Cavalieri Ottolenghi Foundation (NICO), University of Torino, Torino, Italy.
Department of Internal Medicine and Medical Specialties (DIMI), Unit of Geriatric Medicine, University of Genova, Genova, Italy.
J Alzheimers Dis. 2017;59(2):743-751. doi: 10.3233/JAD-170298.
The mechanism of tau toxicity is still unclear. Here we report that recombinant tau oligomers and monomers, intraventricularly injected in mice with a pure human tau background, foster tau pathology through different mechanisms. Oligomeric forms of tau alter the conformation of tau in a paired helical filament-like manner. This effect occurs without tau hyperphosphorylation as well as activation of specific kinases, suggesting that oligomers of tau induce tau assembly through a nucleation effect. Monomers, in turn, induce neurodegeneration through a calpain-mediated tau cleavage that leads to accumulation of a 17 kDa neurotoxic peptide and induction of apoptotic cell death.
tau蛋白毒性的机制仍不清楚。在此我们报告,将重组tau寡聚体和单体经脑室注射到具有纯人类tau背景的小鼠体内,它们通过不同机制促进tau蛋白病变。tau蛋白的寡聚体形式以双螺旋丝状方式改变tau蛋白的构象。这种效应在没有tau蛋白过度磷酸化以及特定激酶激活的情况下发生,这表明tau蛋白寡聚体通过成核效应诱导tau蛋白组装。反过来,单体通过钙蛋白酶介导的tau蛋白裂解诱导神经退行性变,这导致一种17 kDa神经毒性肽的积累并诱导凋亡性细胞死亡。