Watrin Françoise, Manent Jean-Bernard, Cardoso Carlos, Represa Alfonso
INSERM, INMED, Marseille, France; Aix-Marseille University, UMR 901, Marseille, France.
CNS Neurosci Ther. 2015 Feb;21(2):112-22. doi: 10.1111/cns.12322. Epub 2014 Sep 2.
The objective of this article is to review the pathophysiological bases of gray matter heterotopia and to appreciate their involvement in brain cortical development and functional consequences, namely epilepsy. The development of the cerebral cortex results from complex sequential processes including cell proliferation, cell migration, cortical organization, and formation of neuronal networks. Disruption of these steps yields different types of cortical malformations including gray matter heterotopia, characterized by the ectopic position of neurons along the ventricular walls or in the deep white matter. Cortical malformations are major causes of epilepsy, being responsible for up to 40% of drug-resistant epilepsy, and the cognitive level of affected patients varies from normal to severely impaired. This review reports data from human patients and animal models highlighting the genetic causes for these disorders affecting not only neuronal migration but also the proliferation of cortical progenitors. Therefore, gray matter heterotopias should not be considered as solely due to an abnormal neuronal migration and classifying them as such may be too restrictive. The review will also summarize literature data indicating that besides ectopic neurons, neighbor cortical areas also play a consistent role in epileptogenesis, supporting the notion that plastic changes secondary to the initial malformation are instrumental in the pathophysiology of epilepsy in affected patients.
本文的目的是回顾灰质异位症的病理生理基础,并了解其在大脑皮质发育中的作用以及功能后果,即癫痫。大脑皮质的发育源于复杂的连续过程,包括细胞增殖、细胞迁移、皮质组织形成以及神经网络的形成。这些步骤的中断会产生不同类型的皮质畸形,包括灰质异位症,其特征是神经元在脑室壁或深部白质中的异位位置。皮质畸形是癫痫的主要原因,导致高达40%的耐药性癫痫,受影响患者的认知水平从正常到严重受损不等。本综述报告了来自人类患者和动物模型的数据,突出了这些疾病的遗传原因,这些原因不仅影响神经元迁移,还影响皮质祖细胞的增殖。因此,灰质异位症不应仅被视为神经元迁移异常所致,将其如此分类可能过于局限。该综述还将总结文献数据,表明除了异位神经元外,邻近的皮质区域在癫痫发生中也起着重要作用,支持这样一种观点,即继发于初始畸形的可塑性变化在受影响患者癫痫的病理生理学中起重要作用。