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dc.contributor.authorBae, Yeonju-
dc.contributor.authorLee, Soomin-
dc.contributor.authorKim, Ajung-
dc.contributor.authorLee, Shinae-
dc.contributor.authorKim, Seong­Seop-
dc.contributor.authorPark, Sunyoung-
dc.contributor.authorNoh, Junyeol-
dc.contributor.authorRyoo, Kanghyun-
dc.contributor.authorYi, Gwan­Su-
dc.contributor.authorPark, Jae­Yong-
dc.contributor.authorHwang, Eun Mi-
dc.date.accessioned2024-11-20T06:30:05Z-
dc.date.available2024-11-20T06:30:05Z-
dc.date.created2024-11-19-
dc.date.issued2024-11-
dc.identifier.issn0894-1491-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/151113-
dc.description.abstractMature hippocampal astrocytes exhibit a linear current-to-voltage (I-V) K+ membrane conductance called passive conductance. It is estimated to enable astrocytes to keep potassium homeostasis in the brain. We previously reported that the TWIK-1/TREK-1 heterodimeric channels are crucial for astrocytic passive conductance. However, the regulatory mechanism of these channels by other binding proteins remains elusive. Here, we identified Na+/H+ exchange regulator-1 (NHERF-1), a protein highly expressed in astrocytes, as a novel interaction partner for these channels. NHERF-1 endogenously bound to TWIK-1/TREK-1 in hippocampal cultured astrocytes. When NHERF-1 is overexpressed or silenced, surface expression and activity of TWIK-1/TREK-1 heterodimeric channels are inhibited or enhanced, respectively. Furthermore, we confirmed that reduced astrocytic passive conductance by NHERF-1 overexpressing in the hippocampus increases kainic acid (KA)-induced seizure sensitivity. Taken together, these results suggest that NHERF-1 is a key regulator of TWIK-1/TREK-1 heterodimeric channels in astrocytes and suppression of TREK-1 surface expression by NHERF-1 increases KA-induced seizure susceptibility via reduction of astrocytic passive conductance.-
dc.languageEnglish-
dc.publisherJohn Wiley & Sons Inc.-
dc.titleAstrocytic NHERF-1 Increases Seizure Susceptibility by Inhibiting Surface Expression of TREK-1-
dc.typeArticle-
dc.identifier.doi10.1002/glia.24644-
dc.description.journalClass1-
dc.identifier.bibliographicCitationGLIA-
dc.citation.titleGLIA-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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