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癫痫与大脑的可塑性

Epilepsy and the plastic mind.

机构信息

Department of Biology, Program in Neuroscience and Behavior, Hall-Atwater Laboratory, Wesleyan University Middletown, Connecticut, USA.

出版信息

Epilepsy Curr. 2009 Nov-Dec;9(6):166-9. doi: 10.1111/j.1535-7511.2009.01331.x.

Abstract

Seizures are linked to many neuroplastic changes within hippocampal circuits, including alterations in neurogenesis and dendritic growth in the dentate gyrus. How do brief seizures cause the long-term plastic changes in the hippocampus that are associated with recurrent epilepsy? Recent experiments by Ma and colleagues provide insights. They demonstrate an epigenetic mechanism for long-lasting neuroplastic changes that is both activity-dependent and brain region-specific. Focusing on Gadd45b, a DNA excision repair gene, they show it is up-regulated after electroconvulsive seizures or glutamate dependent activation of NMDA receptors. Gadd45b demethylates DNA regulatory elements in promoters of genes encoding fibroblast growth factor 1 and brain-derived neurotrophic factor, increasing the expression of these genes within granule neurons of the dentate gyrus. These changes in growth factor expression promote neurogenesis in the subgranular zone and dendritic growth in the granule cell layer of the dentate gyrus. Further regional and temporal differences in the proliferation of astrocytes and microglia after seizures were demonstrated by two additional studies. Together this work highlights how activity-dependent epigenetic modifications to DNA can alter gene expression with remarkable regional and cell type specificity.

摘要

癫痫发作与海马回路中的许多神经可塑性变化有关,包括神经发生和齿状回树突生长的改变。短暂的癫痫发作如何导致与复发性癫痫相关的海马体的长期可塑性变化?马和同事的最近实验提供了一些见解。他们证明了一种长时程神经可塑性变化的表观遗传机制,这种机制既依赖于活动,又具有大脑区域特异性。他们专注于 Gadd45b,一种 DNA 切除修复基因,发现它在电惊厥后或 NMDA 受体依赖的谷氨酸激活后上调。Gadd45b 使编码成纤维细胞生长因子 1 和脑源性神经营养因子的基因启动子中的 DNA 调节元件去甲基化,增加了颗粒神经元中这些基因的表达。这些生长因子表达的变化促进了齿状回颗粒下区的神经发生和颗粒细胞层的树突生长。另外两项研究进一步证明了癫痫发作后星形胶质细胞和小胶质细胞增殖的区域和时间差异。这项工作共同强调了 DNA 的活性依赖性表观遗传修饰如何以显著的区域和细胞类型特异性改变基因表达。

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