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海马兴奋性毒性损伤后内嗅皮质中细胞周期调节因子和阿尔茨海默病相关蛋白的顺序表达。

Sequential expression of cell-cycle regulators and Alzheimer's disease-related proteins in entorhinal cortex after hippocampal excitotoxic damage.

作者信息

Hernández-Ortega Karina, Ferrera Patricia, Arias Clorinda

机构信息

Departamento de Medicina Genómica y Toxicología Ambiental, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, México.

出版信息

J Neurosci Res. 2007 Jun;85(8):1744-51. doi: 10.1002/jnr.21301.

Abstract

Growing evidence suggests that one of the earliest events in the neuronal degeneration of Alzheimer's disease (AD) is aberrant cell-cycle activation in postmitotic neurons, which may, in fact, be sufficient to initiate the neurodegenerative cascade. In the present study we examined whether cyclins and cyclin-dependent kinases, molecules normally associated with cell-cycle control, may be involved in delayed expression of altered Alzheimer's proteins in two interconnected areas, the entorhinal cortex (EC) and the dentate gyrus (DG), after a hippocampal excitotoxic lesion. Several cell-cycle proteins of the G1 and S phases and even of the G2 phase were found to be up-regulated in the EC after kainic acid evoked neuronal death in the hippocampus. In addition, we describe the progressive expression of two Alzheimer's-related proteins, PHF-1 and APP, which reached higher levels immediately after the increase in G1/S-phase markers. Hence, the results of the present study support the participation of cell-cycle dysregulation as a key component of the process that may ultimately lead to expression of AD proteins and neuronal death in a brain area when the target site for synaptic inputs in that area is damaged by an excitotoxic insult.

摘要

越来越多的证据表明,阿尔茨海默病(AD)神经元变性最早出现的事件之一是有丝分裂后神经元的异常细胞周期激活,事实上,这可能足以启动神经退行性级联反应。在本研究中,我们检测了通常与细胞周期调控相关的细胞周期蛋白和细胞周期蛋白依赖性激酶是否可能参与海马兴奋性毒性损伤后,两个相互连接区域即内嗅皮质(EC)和齿状回(DG)中阿尔茨海默病相关蛋白表达的延迟。在海马内注射 kainic 酸诱发神经元死亡后,发现 EC 中 G1 期、S 期甚至 G2 期的几种细胞周期蛋白上调。此外,我们描述了两种阿尔茨海默病相关蛋白 PHF-1 和 APP 的渐进性表达,它们在 G1/S 期标志物增加后立即达到更高水平。因此,本研究结果支持细胞周期失调作为该过程的关键组成部分参与其中,当该区域的突触输入靶点因兴奋性毒性损伤而受损时,这一过程最终可能导致大脑区域中 AD 蛋白的表达和神经元死亡。

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