Department of Neurology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Department of Neurology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Neuron. 2018 Mar 21;97(6):1284-1298.e7. doi: 10.1016/j.neuron.2018.02.015.
We developed stable isotope labeling and mass spectrometry approaches to measure the kinetics of multiple isoforms and fragments of tau in the human central nervous system (CNS) and in human induced pluripotent stem cell (iPSC)-derived neurons. Newly synthesized tau is truncated and released from human neurons in 3 days. Although most tau proteins have similar turnover, 4R tau isoforms and phosphorylated forms of tau exhibit faster turnover rates, suggesting unique processing of these forms that may have independent biological activities. The half-life of tau in control human iPSC-derived neurons is 6.74 ± 0.45 days and in human CNS is 23 ± 6.4 days. In cognitively normal and Alzheimer's disease participants, the production rate of tau positively correlates with the amount of amyloid plaques, indicating a biological link between amyloid plaques and tau physiology.
我们开发了稳定同位素标记和质谱分析方法,以测量人类中枢神经系统 (CNS) 中以及人诱导多能干细胞 (iPSC) 衍生神经元中 tau 的多种异构体和片段的动力学。新合成的 tau 在 3 天内从人类神经元中截断并释放。尽管大多数 tau 蛋白具有相似的周转率,但 4R tau 异构体和磷酸化形式的 tau 表现出更快的周转率,表明这些形式的独特加工可能具有独立的生物学活性。在对照的人 iPSC 衍生神经元中,tau 的半衰期为 6.74±0.45 天,在人类 CNS 中为 23±6.4 天。在认知正常和阿尔茨海默病患者中,tau 的生成率与淀粉样斑块的数量呈正相关,表明淀粉样斑块和 tau 生理学之间存在生物学联系。