JCI Insight. 2021 Dec 8;6(23):e150120. doi: 10.1172/jci.insight.150120.
Tuberous sclerosis complex (TSC), caused by heterozygous mutations in TSC1 or TSC2, frequently results in intractable epilepsy. Here, we made use of an inducible Tsc1-knockout mouse model, allowing us to study electrophysiological and molecular changes of Tsc1-induced epileptogenesis over time. We recorded from pyramidal neurons in the hippocampus and somatosensory cortex (L2/L3) and combined this with an analysis of transcriptome changes during epileptogenesis. Deletion of Tsc1 resulted in hippocampus-specific changes in excitability and adaptation, which emerged before seizure onset and progressed over time. All phenotypes were rescued after early treatment with rapamycin, an mTOR inhibitor. Later in epileptogenesis, we observed a hippocampal increase of excitation-to-inhibition ratio. These cellular changes were accompanied by dramatic transcriptional changes, especially after seizure onset. Most of these changes were rescued upon rapamycin treatment. Of the genes encoding ion channels or belonging to the Gene Ontology term action potential, 27 were differentially expressed just before seizure onset, suggesting a potential driving role in epileptogenesis. Our data highlight the complex changes driving epileptogenesis in TSC, including the changed expression of multiple ion channels. Our study emphasizes inhibition of the TSC/mTOR signaling pathway as a promising therapeutic approach to target epilepsy in patients with TSC.
结节性硬化症复合征(TSC)是由 TSC1 或 TSC2 中的杂合突变引起的,常导致难治性癫痫。在这里,我们利用诱导型 Tsc1 敲除小鼠模型,研究 Tsc1 诱导的癫痫发生过程中电生理和分子变化的时间进程。我们记录了海马体和体感皮层(L2/L3)中的锥体神经元,并结合癫痫发生过程中的转录组变化进行分析。Tsc1 的缺失导致海马体兴奋性和适应性的特异性变化,这些变化在癫痫发作前出现,并随着时间的推移而进展。在早期用雷帕霉素(mTOR 抑制剂)治疗后,所有表型都得到了挽救。在癫痫发生的后期,我们观察到海马体兴奋-抑制比增加。这些细胞变化伴随着显著的转录变化,特别是在癫痫发作后。雷帕霉素治疗后,这些变化中的大多数都得到了挽救。在编码离子通道或属于动作电位基因本体术语的基因中,有 27 个基因在癫痫发作前表达差异,这表明它们在癫痫发生中具有潜在的驱动作用。我们的数据突出了 TSC 中驱动癫痫发生的复杂变化,包括多个离子通道表达的改变。我们的研究强调抑制 TSC/mTOR 信号通路作为治疗 TSC 患者癫痫的一种有前途的治疗方法。