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)]