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Mice deficient in TWIK-1 are more susceptible to kainic acid-induced seizures

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dc.contributor.authorKim, Ajung-
dc.contributor.authorBae, Yeonju-
dc.contributor.authorGadhe, Changdev G.-
dc.contributor.authorJung, Hyun-Gug-
dc.contributor.authorYang, Esther-
dc.contributor.authorKim, Hyun-
dc.contributor.authorLee, Jaekwang-
dc.contributor.authorShim, Chanseob-
dc.contributor.authorSung, Young Hoon-
dc.contributor.authorNoh, Junyeol-
dc.contributor.authorKim, Eun-Jin-
dc.contributor.authorKang, Dawon-
dc.contributor.authorPae, Ae Nim-
dc.contributor.authorHwang, Eun Mi-
dc.contributor.authorPark, Jae-Yong-
dc.date.accessioned2025-01-02T06:30:12Z-
dc.date.available2025-01-02T06:30:12Z-
dc.date.issued2025-01-
dc.identifier.issn2589-0042-
dc.identifier.issn2589-0042-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/75325-
dc.description.abstractTWIK-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)-
dc.language영어-
dc.language.isoENG-
dc.publisherCELL PRESS-
dc.titleMice deficient in TWIK-1 are more susceptible to kainic acid-induced seizures-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.isci.2024.111587-
dc.identifier.scopusid2-s2.0-85212827667-
dc.identifier.wosid001394599100001-
dc.identifier.bibliographicCitationiScience, v.28, no.1-
dc.citation.titleiScience-
dc.citation.volume28-
dc.citation.number1-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusCHANNEL-
dc.subject.keywordPlusPOTASSIUM-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusKCNK-
dc.subject.keywordAuthorBiological sciences-
dc.subject.keywordAuthorMolecular neuroscience-
dc.subject.keywordAuthorNatural sciences-
dc.subject.keywordAuthorNeuroscience-
dc.subject.keywordAuthorSystems neuroscience-
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