| Literature DB >> 29024662 |
Peijun Li1, Xiaoqin Fu2, Nathan A Smith3, Julie Ziobro3, Julian Curiel3, Milagros J Tenga4, Brandon Martin3, Samuel Freedman5, Christian A Cea-Del Rio5, Livio Oboti3, Tammy N Tsuchida6, Chima Oluigbo7, Amanda Yaun7, Suresh N Magge7, Brent O'Neill8, Amy Kao6, Tesfaye G Zelleke6, Dewi T Depositario-Cabacar6, Svetlana Ghimbovschi9, Susan Knoblach9, Chen-Ying Ho10, Joshua G Corbin3, Howard P Goodkin11, Stefano Vicini12, Molly M Huntsman5, William D Gaillard13, Gregorio Valdez14, Judy S Liu15.
Abstract
Because molecular mechanisms underlying refractory focal epilepsy are poorly defined, we performed transcriptome analysis on human epileptogenic tissue. Compared with controls, expression of Circadian Locomotor Output Cycles Kaput (CLOCK) is decreased in epileptogenic tissue. To define the function of CLOCK, we generated and tested the Emx-Cre; Clockflox/flox and PV-Cre; Clockflox/flox mouse lines with targeted deletions of the Clock gene in excitatory and parvalbumin (PV)-expressing inhibitory neurons, respectively. The Emx-Cre; Clockflox/flox mouse line alone has decreased seizure thresholds, but no laminar or dendritic defects in the cortex. However, excitatory neurons from the Emx-Cre; Clockflox/flox mouse have spontaneous epileptiform discharges. Both neurons from Emx-Cre; Clockflox/flox mouse and human epileptogenic tissue exhibit decreased spontaneous inhibitory postsynaptic currents. Finally, video-EEG of Emx-Cre; Clockflox/flox mice reveals epileptiform discharges during sleep and also seizures arising from sleep. Altogether, these data show that disruption of CLOCK alters cortical circuits and may lead to generation of focal epilepsy.Entities:
Keywords: circadian epilepsy; focal cortical dysplasia; focal epilepsy; tuberous sclerosis complex
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Year: 2017 PMID: 29024662 PMCID: PMC6233318 DOI: 10.1016/j.neuron.2017.09.044
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173