Polenov Neurosurgical Institute-Branch of Almazov National Medical Research Centre, 197341 St. Petersburg, Russia.
Department of Pathology with a Course of Forensic Medicine Named after D.D. Lochov, St. Petersburg State Pediatric Medical University, 194100 St. Petersburg, Russia.
Int J Mol Sci. 2023 Sep 23;24(19):14490. doi: 10.3390/ijms241914490.
The European Commission of the International League Against Epilepsy (ILAE) has identified glial mechanisms of seizures and epileptogenesis as top research priorities. The aim of our study was to conduct a comparative analysis of the expression levels of cytoskeletal proteins (glial fibrillar acidic protein (GFAP) and vimentin), protective protein S100, and proapoptotic caspase-3 protein in patients with drug-resistant epilepsy (DRE) associated with focal cortical dysplasia (FCD). We aimed to investigate how the expression levels of these proteins depend on age (both in children and adults), gender, and disease duration, using immunohistochemistry. Nonparametric statistical methods were employed for data analysis. In the epileptic focus area of the cortex and white matter in patients with FCD-associated temporal lobe DRE, a higher level of expression of these proteins was observed. Age and gender differences were found for vimentin and S100. In the early stages of disease development, there was a compensatory sequential increase in the expression of cytoskeletal and protective proteins. In patients with DRE, depending on the disease duration, patterns of development of neurodegeneration were noted, which is accompanied by apoptosis of gliocytes. These results provide insights into epilepsy mechanisms and may contribute to improving diagnostic and treatment approaches.
国际抗癫痫联盟(ILAE)的欧洲委员会已将神经胶质的癫痫发作和癫痫发生机制确定为优先研究重点。我们的研究目的是通过免疫组织化学比较分析与局灶性皮质发育不良(FCD)相关的耐药性癫痫(DRE)患者的细胞骨架蛋白(胶质纤维酸性蛋白(GFAP)和波形蛋白)、保护蛋白 S100 和促凋亡半胱天冬酶-3 蛋白的表达水平。我们旨在研究这些蛋白的表达水平如何依赖于年龄(儿童和成人)、性别和疾病持续时间。使用非参数统计方法进行数据分析。在 FCD 相关颞叶 DRE 患者的皮质和白质癫痫灶区域,观察到这些蛋白的表达水平更高。发现了波形蛋白和 S100 的年龄和性别差异。在疾病发展的早期阶段,细胞骨架和保护蛋白的表达呈代偿性顺序增加。在 DRE 患者中,根据疾病持续时间,注意到神经退行性变的发展模式,伴有神经胶质细胞凋亡。这些结果提供了对癫痫机制的深入了解,并可能有助于改善诊断和治疗方法。