| Literature DB >> 33348878 |
Yeonju Bae1, Jae Hyouk Choi2, Kanghyun Ryoo1, Ajung Kim2, Osung Kwon1, Hyun-Gug Jung1,2, Eun Mi Hwang2, Jae-Yong Park1.
Abstract
Astrocytes, the most abundant cell type in the brain, are non-excitable cells and play critical roles in brain function. Mature astrocytes typically exhibit a linear current-voltage relationship termed passive conductance, which is believed to enable astrocytes to maintain potassium homeostasis in the brain. We previously demonst<span class="Species">rated that TWIK-1/TREK-1 heterodimeric channels mainly contribute to astrocytic passive conductance. However, the molecular identity of astrocytic passive conductance is still controversial and needs to be elucidated. Here, we report that spadin, an inhibitor of TREK-1, can dramatically reduce astrocytic passive conductance in brain slices. A series of gene silencing experiments demonstrated that spadin-sensitive currents are mediated by TWIK-1/TREK-1 heterodimeric channels in cultured astrocytes and hippocampal astrocytes from brain slices. Our study clearly showed that TWIK-1/TREK-1-heterodimeric channels can act as the main molecular machinery of astrocytic passive conductance, and suggested that spadin can be used as a specific inhibitor to control astrocytic passive conductance.Entities:
Keywords: TWIK-1/TREK-1-heterodimeric channel; astrocyte; astrocytic passive conductance; spadin
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Year: 2020 PMID: 33348878 PMCID: PMC7765948 DOI: 10.3390/ijms21249639
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923