Mice harboring the T316N variant in the GABAAR γ2 subunit exhibit sleep-related hypermotor epilepsy phenotypes and hypersynchronization in the thalamocortical pathway

• Published in: Experimental neurology 2024-06, Vol.376, p.114775-114775, Article 114775
• Main Authors: Jiang, Yong-li, Xia, Liang, Zhao, Jing-jing, Zhou, Hui-min, Mi, Dan, Wang, Xuan, Wang, Yuan-yuan, Song, Chang-geng, Jiang, Wen
• Format: Article
• Language: English
• Subjects: GABRG2; Gabrg2T316N/+ knock-in mice; Sleep-related hypermotor epilepsy; Thalamocortical loop; γ-Aminobutyric acid type a receptor; γ2 subunit
• ISSN: 0014-4886; 1090-2430
• DOI: 10.1016/j.expneurol.2024.114775

Sleep-related hypermotor epilepsy (SHE) is a focal epilepsy syndrome characterized by seizures that predominantly occur during sleep. The pathogenesis of these seizures remains unclear. We previously detected rare variants in GABRG2, which encodes the γ2 subunit of γ-aminobutyric acid type A receptor (GABAAR), in patients with SHE and demonstrated that these variants impaired GABAAR function in vitro. However, the mechanisms by which GABRG2 variants contribute to seizure attacks during sleep remain unclear. In this study, we designed a knock-in (KI) mouse expressing the mouse Gabrg2 T316N variant, corresponding to human GABRG2 T317N variant, using CRISPR/Cas9. Continuous video-electroencephalogram monitoring and in vivo multichannel electrophysiological recordings were performed to explore seizure susceptibility to pentylenetetrazol (PTZ), alterations in the sleep-wake cycle, spontaneous seizure patterns, and synchronized activity in the motor thalamic nuclei (MoTN) and secondary motor cortex (M2). Circadian variations in the expression of total, membrane-bound, and synaptic GABAAR subunits were also investigated. No obvious changes in gross morphology were detected in Gabrg2T316N/+ mice compared to their wild-type (Gabrg2+/+) littermates. Gabrg2T316N/+ mice share key phenotypes with patients, including sleep fragmentation and spontaneous seizures during sleep. Gabrg2T316N/+ mice showed increased susceptibility to PTZ-induced seizures and higher mortality after seizures. Synchronization of the local field potentials between the MoTN and M2 was abnormally enhanced in Gabrg2T316N/+ mice during light phase, when sleep dominates, accompanied by increased local activities in the MoTN and M2. Interestingly, in Gabrg2+/+ mice, GABAAR γ2 subunits showed a circadian increase on the neuronal membrane and synaptosomes in the transition from dark phase to light phase, which was absent in Gabrg2T316N/+ mice. We generated a new SHE mouse model and provided in vivo evidence that rare variants of GABRG2 contribute to seizure attacks during sleep in SHE. •Mice harboring the T316N variant in GABAAR γ2 subunit are originally constructed.•Gabrg2T316N/+ knock-in mice have spontaneous seizures mainly occurring during daytime.•NREM sleep is fragmented by brief awakening events in Gabrg2T316N/+ knock-in mice.•Gabrg2T316N/+ knock-in mice have enhanced synchronization between MoTN and M2.•Circadian change in membrane γ2 subunit is absent in Gabrg2T316N/+ knock-in mice.