Fu Pengfei, Wen YueTao, Xiong Yan, Zhang Yanke, Zhang Haiyang, Xie Yanfeng, Shi Quanhong
Department of Neurosurgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Department of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Neurochem Res. 2016 Nov;41(11):3020-3031. doi: 10.1007/s11064-016-2021-y. Epub 2016 Aug 8.
E3 ubiquitin ligases are important protein-modifying enzymes involved in the pathogenesis of a variety of neurodegenerative diseases. F-box and leucine-rich repeat protein 20 (FBXL20), an E3 ubiquitin ligase widely expressed in the central nervous system, plays an important role in the ubiquitin-dependent degradation of regulating synaptic membrane exocytosis 1 (RIM1), which is an important factor in the release of synaptic vesicles. FBXL20 has been associated with a variety of neurodegenerative diseases; thus, we hypothesized that FBXL20 is involved in the development of epilepsy. Herein, we used immunofluorescence staining, immunohistochemistry and western blotting to determine the expression pattern of FBXL20 in temporal lobe epilepsy patients and pilocarpine-induced epilepsy animal models. We also injected SD rats with lentivirus-vector mediated overexpression of FBXL20. The results showed that FBXL20 is expressed in the membrane and the cytoplasm of cortical neurons, and overexpression of FBXL20 decreased the onset level of spontaneous seizure, the frequency and duration of seizures. Additionally, FBXL20 protein level was decreased but RIM1 protein level was increased in the epileptic group compared with the LV-FBXL20 and LV-GFP group. These findings in humans were consistent with the results from a pilocarpine-induced animal model of chronic epilepsy. Thus, abnormal expression of FBXL20 might play an important role in the development of epilepsy.
E3泛素连接酶是参与多种神经退行性疾病发病机制的重要蛋白质修饰酶。F-box和富含亮氨酸重复序列蛋白20(FBXL20)是一种在中枢神经系统广泛表达的E3泛素连接酶,在调节突触膜胞吐作用1(RIM1)的泛素依赖性降解中起重要作用,而RIM1是突触小泡释放的一个重要因素。FBXL20已与多种神经退行性疾病相关;因此,我们推测FBXL20参与癫痫的发生发展。在此,我们使用免疫荧光染色、免疫组织化学和蛋白质印迹法来确定FBXL20在颞叶癫痫患者和毛果芸香碱诱导的癫痫动物模型中的表达模式。我们还向SD大鼠注射慢病毒载体介导的FBXL20过表达。结果显示,FBXL20在皮质神经元的细胞膜和细胞质中表达,FBXL20的过表达降低了自发癫痫发作的起始水平、发作频率和持续时间。此外,与LV-FBXL20和LV-GFP组相比,癫痫组中FBXL20蛋白水平降低,但RIM1蛋白水平升高。这些在人类中的发现与毛果芸香碱诱导的慢性癫痫动物模型的结果一致。因此,FBXL20的异常表达可能在癫痫的发生发展中起重要作用。