Department of Neurology, Washington University School of Medicine, St Louis, MO.
Hope Center for Neurological Disorders, Washington University School of Medicine, St Louis, MO.
Ann Neurol. 2020 May;87(5):700-709. doi: 10.1002/ana.25702. Epub 2020 Feb 27.
Tau hyperphosphorylation is an early step in tau-mediated neurodegeneration and is associated with intracellular aggregation of tau as neurofibrillary tangles, neuronal and synaptic loss, and eventual cognitive dysfunction in Alzheimer disease. Sleep loss increases the cerebrospinal fluid concentration of amyloid-β and tau. Using mass spectrometry, we measured tau and phosphorylated tau concentrations in serial samples of cerebrospinal fluid collected from participants who were sleep-deprived, treated with sodium oxybate, or allowed to sleep normally. We found that sleep loss affected phosphorylated tau differently depending on the modified site. These findings suggest a mechanism for sleep loss to increase risk of Alzheimer disease. ANN NEUROL 2020;87:700-709.
tau 过度磷酸化是 tau 介导的神经退行性变的早期步骤,与 tau 作为神经原纤维缠结的细胞内聚集、神经元和突触丢失以及阿尔茨海默病的最终认知功能障碍有关。睡眠缺失会增加脑脊液中淀粉样蛋白-β和 tau 的浓度。我们使用质谱法测量了睡眠剥夺、接受羟丁酸钠治疗或正常睡眠的参与者连续脑脊液样本中的 tau 和磷酸化 tau 浓度。我们发现,根据修饰部位的不同,睡眠缺失对磷酸化 tau 的影响也不同。这些发现为睡眠缺失增加阿尔茨海默病风险提供了一种机制。ANN NEUROL 2020;87:700-709。