Mice deficient in TWIK-1 are more susceptible to kainic acid-induced seizuresopen access
- Authors
- Kim, Ajung; Bae, Yeonju; Gadhe, Changdev G.; Jung, Hyun-Gug; Yang, Esther; Kim, Hyun; Lee, Jaekwang; Shim, Chanseob; Sung, Young Hoon; Noh, Junyeol; Kim, Eun-Jin; Kang, Dawon; Pae, Ae Nim; Hwang, Eun Mi; Park, Jae-Yong
- Issue Date
- Jan-2025
- Publisher
- CELL PRESS
- Keywords
- Biological sciences; Molecular neuroscience; Natural sciences; Neuroscience; Systems neuroscience
- Citation
- iScience, v.28, no.1
- Indexed
- SCIE
SCOPUS
- Journal Title
- iScience
- Volume
- 28
- Number
- 1
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/75325
- DOI
- 10.1016/j.isci.2024.111587
- ISSN
- 2589-0042
2589-0042
- Abstract
- TWIK-1 belongs to the two-pore domain K+ (K2P) channel family, which plays an essential role in the background K+ conductance of cells. Despite the development of exon 2-deleted Twik-1 knockout (KO) mice, the physiological role of TWIK-1 has remained largely unknown. Here, we observed that the exon 2-deleted Twik-1 KO mice expressed an internally deleted TWIK-1 (TWIK-1 ΔEx2) protein, which unexpectedly acts as a functional K+ channel. The Twik-1 nKO mice in which exon 1 was targeted using the CRISPR-Cas9 technique provides strong evidence that TWIK-1 mediates K+ currents that are responsible for the background passive conductance in astrocytes. Deficiency of TWIK-1-mediated astrocytic passive conductance increased susceptibility to kainic acid-induced seizures. This study paves the way for functional studies on TWIK-1-mediated astrocytic passive conductance. In addition, the exon 1-targeted Twik-1 KO mice would help elucidate the physiological roles of TWIK-1. © 2024 The Author(s)
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