Notch Signaling Regulates Microglial Activation and Inflammatory Reactions in a Rat Model of Temporal Lobe Epilepsy

被引:36
|
作者
Wu, Lei [1 ]
Li, Yushuang [1 ]
Yu, Minhua [1 ]
Yang, Fei [1 ]
Tu, Mengqi [1 ]
Xu, Haibo [1 ]
机构
[1] Wuhan Univ, Zhongnan Hosp, Dept Radiol, Wuhan 430071, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Epilepsy; Notch signaling; Microglia; Inflammation; Apoptosis; MURINE BV-2 CELLS; STATUS EPILEPTICUS; KAPPA-B; AMEBOID MICROGLIA; SEIZURE ACTIVITY; EXPRESSION; CYTOKINES; BRAIN; PATHWAY; COMPLEX;
D O I
10.1007/s11064-018-2544-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The inflammatory response mediated by microglia in the central nervous system is closely related to epilepsy. Notch signaling plays an important role in the microglial activation during hypoxia. This study aimed to investigate whether Notch signaling is involved in microglial activation and subsequent inflammation-related neuronal injury during the process of epileptogenesis in a rat model of temporal lobe epilepsy. By using western blotting, real-time quantitative PCR, immunohistochemistry and immunofluorescence labeling, we found that the expression of Notch signaling increased after status epilepticus and that a gamma-secretase inhibitor could significantly inhibit the upregulation of Notch signaling, the activation of microglia, and the release of proinflammatory cytokines. Likewise, the neuronal apoptosis and loss in the hippocampus after SE were attenuated by the gamma-secretase inhibitor. These results suggest that Notch signaling plays a key role in neuroinflammation and inflammation-related neuronal damage in epilepsy, and gamma-secretase inhibitors may become a novel prospective therapeutic agent for epilepsy.
引用
收藏
页码:1269 / 1282
页数:14
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