ナカヤマ ヒサコ
Hisako Nakayama
中山 寿子 所属 医学部 医学科 職種 准教授 |
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論文種別 | 原著 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Ionic Basis for Membrane Potential Resonance in Neurons of the Inferior Olive. |
掲載誌名 | 正式名:Cell Reports 略 称:Cell Rep ISSNコード:22111247 |
掲載区分 | 国外 |
巻・号・頁 | 16(4),pp.994-1004 |
著者・共著者 | MATSUMOTO-MAKIDONO Yoshiko†, NAKAYAMA Hisako, YAMASAKI Miwako, MIYAZAKI Taisuke, WATANABE Masahiko, KANO Masanobu, SAKIMURA Kenji, HASHIMOTO Kouichi* |
担当区分 | 2nd著者 |
発行年月 | 2016/07 |
概要 | Some neurons have the ability to enhance output voltage to input current with a preferred frequency, which is called resonance. Resonance is thought to be a basis for membrane potential oscillation. Although ion channels responsible for resonance have been reported, the precise mechanisms by which these channels work remain poorly understood. We have found that resonance is reduced but clearly present in the inferior olivary neurons of Cav3.1 T-type voltage-dependent Ca(2+) channel knockout (KO) mice. The activation of Cav3.1 channels is strongly membrane potential dependent, but less frequency dependent. Residual resonance in Cav3.1 KO mice is abolished by a hyper-polarization-activated cyclic nucleotide-gated (HCN) channel blocker, ZD7288, and is partially suppressed by voltage-dependent K(+) channel blockers. Resonance is inhibited by ZD7288 in wild-type mice and impaired in HCN1 KO mice, suggesting that the HCN1 channel is essential for resonance. The ZD7288-sensitive current is nearly sinusoidal and strongly frequency dependent. These results suggest that Cav3.1 and HCN1 channels act as amplifying and resonating conductances, respectively. |
DOI | 10.1016/j.celrep.2016.06.053. |
PMID | 27425615 |