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年龄相关的可溶性淀粉样蛋白β(Abeta)寡聚体的积累通过调节阿尔茨海默病小鼠模型中的磷酸肌醇 3-激酶(PI3K)/Akt-GSK-3β通路逆转可溶性淀粉样前体蛋白-α(sAPP(alpha))的神经保护作用。

Age-dependent accumulation of soluble amyloid beta (Abeta) oligomers reverses the neuroprotective effect of soluble amyloid precursor protein-alpha (sAPP(alpha)) by modulating phosphatidylinositol 3-kinase (PI3K)/Akt-GSK-3beta pathway in Alzheimer mouse model.

机构信息

Departamento Bioquímica y Biología Molecular, Facultad de Farmacia, Universidad de Sevilla, 41012 Sevilla, Spain.

出版信息

J Biol Chem. 2011 May 27;286(21):18414-25. doi: 10.1074/jbc.M110.209718. Epub 2011 Apr 1.

Abstract

Neurotrophins, activating the PI3K/Akt signaling pathway, control neuronal survival and plasticity. Alterations in NGF, BDNF, IGF-1, or insulin signaling are implicated in the pathogenesis of Alzheimer disease. We have previously characterized a bigenic PS1×APP transgenic mouse displaying early hippocampal Aβ deposition (3 to 4 months) but late (17 to 18 months) neurodegeneration of pyramidal cells, paralleled to the accumulation of soluble Aβ oligomers. We hypothesized that PI3K/Akt/GSK-3β signaling pathway could be involved in this apparent age-dependent neuroprotective/neurodegenerative status. In fact, our data demonstrated that, as compared with age-matched nontransgenic controls, the Ser-9 phosphorylation of GSK-3β was increased in the 6-month PS1×APP hippocampus, whereas in aged PS1×APP animals (18 months), GSK-3β phosphorylation levels displayed a marked decrease. Using N2a and primary neuronal cell cultures, we demonstrated that soluble amyloid precursor protein-α (sAPPα), the predominant APP-derived fragment in young PS1×APP mice, acting through IGF-1 and/or insulin receptors, activated the PI3K/Akt pathway, phosphorylated the GSK-3β activity, and in consequence, exerted a neuroprotective action. On the contrary, several oligomeric Aβ forms, present in the soluble fractions of aged PS1×APP mice, inhibited the induced phosphorylation of Akt/GSK-3β and decreased the neuronal survival. Furthermore, synthetic Aβ oligomers blocked the effect mediated by different neurotrophins (NGF, BDNF, insulin, and IGF-1) and sAPPα, displaying high selectivity for NGF. In conclusion, the age-dependent appearance of APP-derived soluble factors modulated the PI3K/Akt/GSK-3β signaling pathway through the major neurotrophin receptors. sAPPα stimulated and Aβ oligomers blocked the prosurvival signaling. Our data might provide insights into the selective vulnerability of specific neuronal groups in Alzheimer disease.

摘要

神经递 质,通过激活 PI3K/Akt 信号通路,控制神经元的存活和可塑性。NGF、BDNF、IGF-1 或胰岛素信号的改变与阿尔茨海默病的发病机制有关。我们之前已经描述了一种双转基因 PS1×APP 转基因小鼠,其具有早期海马 Aβ 沉积(3 至 4 个月),但晚期(17 至 18 个月)锥体神经元发生神经退行性变,与可溶性 Aβ 寡聚物的积累平行。我们假设 PI3K/Akt/GSK-3β 信号通路可能参与这种明显的年龄依赖性神经保护/神经退行性状态。事实上,我们的数据表明,与年龄匹配的非转基因对照相比,6 个月 PS1×APP 海马体中的 GSK-3β Ser-9 磷酸化增加,而在老年 PS1×APP 动物(18 个月)中,GSK-3β 磷酸化水平显著降低。使用 N2a 和原代神经元细胞培养物,我们证明了可溶性淀粉样前体蛋白-α(sAPPα),即年轻 PS1×APP 小鼠中主要的 APP 衍生片段,通过 IGF-1 和/或胰岛素受体起作用,激活了 PI3K/Akt 通路,磷酸化了 GSK-3β 的活性,从而发挥了神经保护作用。相反,几种寡聚 Aβ 形式存在于老年 PS1×APP 小鼠的可溶性部分中,抑制了 Akt/GSK-3β 的诱导磷酸化,并降低了神经元的存活率。此外,合成的 Aβ 寡聚物阻断了不同神经营养因子(NGF、BDNF、胰岛素和 IGF-1)和 sAPPα 介导的作用,对 NGF 表现出高选择性。总之,APP 衍生的可溶性因子的年龄依赖性出现通过主要的神经营养因子受体调节了 PI3K/Akt/GSK-3β 信号通路。sAPPα 刺激而 Aβ 寡聚物阻断了促生存信号。我们的数据可能为阿尔茨海默病中特定神经元群体的选择性易损性提供了一些见解。

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