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通过 T668 磷酸化的细胞表面 APP 抑制神经元钙振荡。

Inhibition of neuronal calcium oscillations by cell surface APP phosphorylated on T668.

机构信息

Université catholique de Louvain, Institute of Neuroscience, B-1200 Brussels, Belgium.

出版信息

Neurobiol Aging. 2011 Dec;32(12):2308-13. doi: 10.1016/j.neurobiolaging.2010.01.006. Epub 2010 Feb 1.

Abstract

Adenoviral expression of human APP (hAPP), but not of hAPP deleted from its C-terminal intracellular domain, in rat cortical neurons abolishes spontaneous synchronous calcium oscillations. The intracellular domain of APP695 contains several residues that can be phosphorylated. Contrary to non-neuronal cells, a very high phosphorylation of APP on T668 is observed in neurons, which is mediated by JNK, GSK3 and Cdk5 protein kinases. JNK activity, modulated by GSK3, enhances the traffic of phosphorylated APP to nerve terminals, contrary to Cdk5. Here we show that inhibition of GSK3 and JNK restores calcium oscillations in an hAPP expressing neuronal network, whereas inhibition of Cdk5 does not. Expression of mutant hAPPT668A does not inhibit calcium oscillations, and the proportion of hAPPT668A at the plasma membrane is reduced by more than 50%. Altogether, these results indicate that the intracellular domain of APP is needed to inhibit neuronal calcium oscillations because GSK3/JNK phosphorylation of T668 controls APP trafficking at the plasma membrane.

摘要

腺病毒表达的人淀粉样前体蛋白(hAPP),但不是从其 C 端细胞内结构域缺失的 hAPP,在大鼠皮质神经元中可消除自发性同步钙振荡。APP695 的细胞内结构域含有几个可磷酸化的残基。与非神经元细胞不同,在神经元中观察到 APP 在 T668 上的高度磷酸化,这是由 JNK、GSK3 和 Cdk5 蛋白激酶介导的。由 GSK3 调节的 JNK 活性增强了磷酸化 APP 向神经末梢的运输,而不是 Cdk5。在这里,我们表明抑制 GSK3 和 JNK 可恢复表达 hAPP 的神经元网络中的钙振荡,而抑制 Cdk5 则不能。表达突变型 hAPPT668A 不会抑制钙振荡,并且 hAPPT668A 在质膜上的比例减少了 50%以上。总之,这些结果表明 APP 的细胞内结构域是抑制神经元钙振荡所必需的,因为 T668 的 GSK3/JNK 磷酸化控制着 APP 在质膜上的运输。

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