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癫痫齿状回的蛋白质组学分析。

Proteomic profiling of the epileptic dentate gyrus.

机构信息

Key Lab. for Organ Failure Research, Education Ministry of P.R. China, Southern Medical University, Guangzhou, China.

出版信息

Brain Pathol. 2010 Nov;20(6):1077-89. doi: 10.1111/j.1750-3639.2010.00414.x. Epub 2010 Jul 4.

Abstract

The development of epilepsy is often associated with marked changes in central nervous system cell structure and function. Along these lines, reactive gliosis and granule cell axonal sprouting within the dentate gyrus of the hippocampus are commonly observed in individuals with temporal lobe epilepsy (TLE). Here we used the pilocarpine model of TLE in mice to screen the proteome and phosphoproteome of the dentate gyrus to identify molecular events that are altered as part of the pathogenic process. Using a two-dimensional gel electrophoresis-based approach, followed by liquid chromatography-tandem mass spectrometry, 24 differentially expressed proteins, including 9 phosphoproteins, were identified. Functionally, these proteins were organized into several classes, including synaptic physiology, cell structure, cell stress, metabolism and energetics. The altered expression of three proteins involved in synaptic physiology, actin, profilin 1 and α-synuclein was validated by secondary methods. Interestingly, marked changes in protein expression were detected in the supragranular cell region, an area where robust mossy fibers sprouting occurs. Together, these data provide new molecular insights into the altered protein profile of the epileptogenic dentate gyrus and point to potential pathophysiologic mechanisms underlying epileptogenesis.

摘要

癫痫的发展通常与中枢神经系统细胞结构和功能的显著变化有关。沿着这些思路,在颞叶癫痫(TLE)患者的海马齿状回中,反应性神经胶质增生和颗粒细胞轴突发芽是常见的。在这里,我们使用匹鲁卡品诱导的 TLE 小鼠模型,筛选齿状回的蛋白质组和磷酸化蛋白质组,以确定作为致病过程一部分而改变的分子事件。使用基于二维凝胶电泳的方法,然后进行液相色谱-串联质谱分析,鉴定出 24 种差异表达蛋白,包括 9 种磷酸化蛋白。从功能上看,这些蛋白被组织成几个类别,包括突触生理学、细胞结构、细胞应激、代谢和能量学。通过二次方法验证了参与突触生理学的三种蛋白(肌动蛋白、原肌球蛋白 1 和α-突触核蛋白)的表达改变。有趣的是,在颗粒上层细胞区域(此处发生强烈的苔藓纤维发芽)检测到蛋白质表达的显著变化。总之,这些数据为致痫性齿状回改变的蛋白质图谱提供了新的分子见解,并指出了癫痫发生的潜在病理生理机制。

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