Battaglia Giorgio, Becker Albert J, LoTurco Joseph, Represa Alfonso, Baraban Scott C, Roper Steven N, Vezzani Annamaria
Molecular Neuroanatomy and Pathogenesis Unit, IRCCS Foundation Neurological Institute Carlo Besta, Milano, Italy.
Epileptic Disord. 2009 Sep;11(3):206-14. doi: 10.1684/epd.2009.0273. Epub 2009 Sep 10.
Epilepsy-associated glioneuronal malformations (malformations of cortical development [MCD]) include focal cortical dysplasias (FCD) and highly differentiated glioneuronal tumors, most frequently gangliogliomas. The neuropathological findings are variable but suggest aberrant proliferation, migration, and differentiation of neural precursor cells as essential pathogenetic elements. Recent advances in animal models for MCDs allow new insights in the molecular pathogenesis of these epilepsy-associated lesions. Novel approaches, presented here, comprise RNA interference strategies to generate and study experimental models of subcortical band heterotopia and study functional aspects of aberrantly shaped and positioned neurons. Exciting analyses address impaired NMDA receptor expression in FCD animal models compared to human FCDs and excitatory imbalances in MCD animal models such as lissencephaly gene ablated mice as well as in utero irradiated rats. An improved understanding of relevant pathomechanisms will advance the development of targeted treatment strategies for epilepsy-associated malformations.
癫痫相关的神经胶质神经元畸形(皮质发育畸形[MCD])包括局灶性皮质发育异常(FCD)和高度分化的神经胶质神经元肿瘤,最常见的是神经节细胞胶质瘤。神经病理学发现各不相同,但提示神经前体细胞的异常增殖、迁移和分化是关键的致病因素。MCD动物模型的最新进展为深入了解这些癫痫相关病变的分子发病机制提供了新的视角。本文介绍的新方法包括RNA干扰策略,用于生成和研究皮质下带状异位的实验模型,并研究形状和位置异常的神经元的功能方面。令人兴奋的分析涉及与人类FCD相比,FCD动物模型中NMDA受体表达受损的情况,以及MCD动物模型中的兴奋性失衡,如无脑回基因敲除小鼠和子宫内照射大鼠。对相关发病机制的更好理解将推动针对癫痫相关畸形的靶向治疗策略的发展。