TSC1
癫痫发生
星形胶质细胞
结节性硬化
谷氨酸受体
神经科学
癫痫
胶质纤维酸性蛋白
生物
TSC2
细胞生物学
病理
医学
中枢神经系统
免疫学
生物化学
PI3K/AKT/mTOR通路
免疫组织化学
受体
信号转导
作者
Michael Wong,Kevin C. Ess,Erik J. Uhlmann,Laura A. Jansen,Wen Li,Peter B. Crino,Steven Mennerick,Kelvin A. Yamada,David H. Gutmann
摘要
Abstract Excessive astrocytosis in cortical tubers in tuberous sclerosis complex (TSC) suggests that astrocytes may be important for epileptogenesis in TSC. We previously demonstrated that astrocyte‐specific Tsc1 gene inactivation in mice ( Tsc1 cKO mice) results in progressive epilepsy. Here, we report that glutamate transporter expression and function is impaired in Tsc1 cKO astrocytes. Tsc1 cKO mice exhibit decreased GLT‐1 and GLAST protein expression. Electrophysiological assays demonstrate a functional decrease in glutamate transport currents of Tsc1 cKO astrocytes in hippocampal slices and astrocyte cultures. These findings suggest that Tsc1 inactivation in astrocytes causes dysfunctional glutamate homeostasis, leading to seizure development in TSC. Ann Neurol 2003
科研通智能强力驱动
Strongly Powered by AbleSci AI