日本生理学会大会発表要旨集
セッションID: 1P231
会議情報
S125 Ionic channels & receptors
ヒト近位尿細管BKチャネルの開口確率上昇に対する細胞内Ca2+およびMg2+の効果とそのゲート機構の比較
平野 順子中村 一芳久保川 学
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会議録・要旨集 フリー

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抄録
The Ca2+-activated BK channel in cultured human proximal tubule cells (RPTECs) is sensitive to voltage, ATP, and pHi. Furthermore, we recently found out that this channel was regulated also by intracellular Mg2+ ([Mg2+]i). One of the significant effects of [Mg2+]i on channel was to extend the open time at a low intracellular Ca2+ ([Ca2+]i). However, [Mg2+]i effect on channel under the relatively high [Ca2+]i is still unknown. In this study, we examined effects of [Mg2+]i (1 - 10 mM) on open probability (Po) and gating mechanisms of the BK channel in the presence of 0.1 - 1.0 mM [Ca2+]i, and compared with the gating of high [Ca2+]i-induced channel activation, using the patch-clamp technique. When the channel was activated by 0.1 mM [Ca2+]i, raising [Mg2+]i up to 10 mM elevated Po and induced parallel shifts of Po - Vm relationships. These effects of [Mg2+]i on channel Po and the Po - Vm relationships were mimicked by either total or partial substitution of equimolar [Mg2+]i to [Ca2+]i. In the presence of 1 mM [Ca2+]i, addition of 10 mM [Mg2+]i further enhanced channel Po, which was also similar to channel activation by raising [Ca2+]i to 10 mM. The dwell-time histograms obtained from 10 mM [Mg2+]i in the presence of 0.1 mM [Ca2+]iwere similar to that obtained from 10 mM [Ca2+]i. These results suggest that, in addition to high affinity Ca2+-binding sites, the BK channel in RPTECs possesses the binding site for both Ca2+ and Mg2+, which is involved in channel activation, and its affinity ratio of Ca2+/ Mg2+ is close to 1. [Jpn J Physiol 54 Suppl:S128 (2004)]
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© 2004 日本生理学会
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