Key result
BK channels with ~70 pS conductance mediate fast persistent Ca2+-activated K+ currents in crayfish muscle.
The Ca2+-activated K+ current in crayfish muscle is mediated by fast, voltage- and Ca2+-gated BK channels with relatively small conductance that act as precise Ca2+ sensors.
No immediate clinical implications; extends invertebrate BK channel characterization and leaves open mammalian cardiac relevance.
The role of the Ca(2+)-activated K(+) current (I(K(Ca))) in crayfish opener muscle fibers is functionally important because it regulates the graded electrical activity that is characteristic of these fibers. Using the cell-attached and inside-out configurations of the patch-clamp technique, we found three different classes of channels with properties that matched those expected of the three different ionic channels mediating the depolarization-activated macroscopic currents previously described (Ca(2+), K(+), and Ca(2+)-dependent K(+) currents). We investigated the properties of the ionic channels mediating the extremely fast activating and persistent I(K(Ca)). These voltage- and Ca(2+)-activated channels had a mean single-channel conductance of approximately 70 pS and showed a very fast activation. Both the single-channel open probability and the speed of activation increased with depolarization. Both parameters also increased in inside-out patches, i.e., in high Ca(2+) concentration. Intracellular loading with the Ca(2+) chelator bis(2-aminophenoxy) ethane-N, N,N',N'-tetraacetic acid gradually reduced and eventually prevented channel openings. The channels opened at very brief delays after the pulse depolarization onset (<5 ms), and the time-dependent open probability was constant during sustained depolarization (< or =560 ms), matching both the extremely fast activation kinetics and the persistent nature of the macroscopic I(K(Ca)). However, the intrinsic properties of these single channels do not account for the partial apparent inactivation of the macroscopic I(K(Ca)), which probably reflects temporal Ca(2+) variations in the whole muscle fiber. We conclude that the channels mediating I(K(Ca)) in crayfish muscle are voltage- and Ca(2+)-gated BK channels with relatively small conductance. The intrinsic properties of these channels allow them to act as precise Ca(2+) sensors that supply the exact feedback current needed to control the graded electrical activity and therefore the contraction of opener muscle fibers.
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Araque et al. (1999) studied Crayfish opener muscle fibers. Patch-clamp technique and intracellular loading with BAPTA was evaluated on Single-channel conductance and activation properties. In crayfish opener muscle fibers, the extremely fast activating and persistent Ca2+-activated K+ current is mediated by voltage- and Ca2+-gated BK channels with a mean conductance of ~70 pS.
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