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

Copyright © 2023. Published by Elsevier Inc..

OBJECTIVE: 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.

METHODS: 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.

RESULTS: 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.

CONCLUSION: 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.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:376

Enthalten in:

Experimental neurology - 376(2024) vom: 09. Apr., Seite 114775

Sprache:

Englisch

Beteiligte Personen:

Jiang, Yong-Li [VerfasserIn]
Xia, Liang [VerfasserIn]
Zhao, Jing-Jing [VerfasserIn]
Zhou, Hui-Min [VerfasserIn]
Mi, Dan [VerfasserIn]
Wang, Xuan [VerfasserIn]
Wang, Yuan-Yuan [VerfasserIn]
Song, Chang-Geng [VerfasserIn]
Jiang, Wen [VerfasserIn]

Links:

Volltext

Themen:

γ-Aminobutyric acid type a receptor
γ2 subunit
GABRG2
Gabrg2(T316N/+) knock-in mice
Journal Article
Sleep-related hypermotor epilepsy
Thalamocortical loop

Anmerkungen:

Date Revised 14.04.2024

published: Print-Electronic

Citation Status Publisher

doi:

10.1016/j.expneurol.2024.114775

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM370937589