高脂饮食诱导的 SGK1 激活促进了阿尔茨海默病相关的 tau 病理。
High-fat diet-induced activation of SGK1 promotes Alzheimer's disease-associated tau pathology.
机构信息
Department of Diagnosis, Prevention and Treatment of Dementia, Juntendo University Graduate of Medicine, Tokyo, Japan.
Department of Neurology, Juntendo University Graduate of Medicine, Tokyo, Japan.
出版信息
Hum Mol Genet. 2021 Aug 28;30(18):1693-1710. doi: 10.1093/hmg/ddab115.
Type 2 diabetes mellitus (T2DM) has long been considered a risk factor for Alzheimer's disease (AD). However, the molecular links between T2DM and AD remain obscure. Here, we reported that serum-/glucocorticoid-regulated kinase 1 (SGK1) is activated by administering a chronic high-fat diet (HFD), which increases the risk of T2DM, and thus promotes Tau pathology via the phosphorylation of tau at Ser214 and the activation of a key tau kinase, namely, GSK-3ß, forming SGK1-GSK-3ß-tau complex. SGK1 was activated under conditions of elevated glucocorticoid and hyperglycemia associated with HFD, but not of fatty acid-mediated insulin resistance. Elevated expression of SGK1 in the mouse hippocampus led to neurodegeneration and impairments in learning and memory. Upregulation and activation of SGK1, SGK1-GSK-3ß-tau complex were also observed in the hippocampi of AD cases. Our results suggest that SGK1 is a key modifier of tau pathology in AD, linking AD to corticosteroid effects and T2DM.
2 型糖尿病(T2DM)长期以来一直被认为是阿尔茨海默病(AD)的一个危险因素。然而,T2DM 和 AD 之间的分子联系仍然不清楚。在这里,我们报道了血清/糖皮质激素调节激酶 1(SGK1)在给予慢性高脂肪饮食(HFD)后被激活,HFD 会增加 T2DM 的风险,从而通过磷酸化 tau 丝氨酸 214 和激活关键的 tau 激酶即 GSK-3ß,形成 SGK1-GSK-3ß-tau 复合物来促进 Tau 病理。SGK1 在与 HFD 相关的升高的糖皮质激素和高血糖条件下被激活,但不是在脂肪酸介导的胰岛素抵抗下被激活。在小鼠海马中升高的 SGK1 表达导致神经退行性变和学习记忆受损。AD 病例中海马中也观察到 SGK1、SGK1-GSK-3ß-tau 复合物的上调和激活。我们的结果表明,SGK1 是 AD 中 Tau 病理的关键修饰物,将 AD 与皮质类固醇效应和 T2DM 联系起来。