BK <sub>Ca</sub> -Cav Channel Complexes Mediate Rapid and Localized Ca <sup>2+</sup> -Activated K <sup>+</sup> Signaling

Henrike Berkefeld(Innsbruck Medical University), Claudia A. Sailer(Innsbruck Medical University), Wolfgang Bildl(Innsbruck Medical University), V. Rohde(Innsbruck Medical University), Jörg Oliver Thumfart(Innsbruck Medical University), Silke Eble(Innsbruck Medical University), Norbert Klugbauer(Innsbruck Medical University), Ellen Reisinger(Innsbruck Medical University), Josef Bischofberger(Innsbruck Medical University), Dominik Oliver(Innsbruck Medical University), Hans‐Günther Knaus(Innsbruck Medical University), Uwe Schulte(Innsbruck Medical University), Bernd Fakler(Innsbruck Medical University)
Science
October 26, 2006
Cited by 377

Abstract

Large-conductance calcium- and voltage-activated potassium channels (BKCa) are dually activated by membrane depolarization and elevation of cytosolic calcium ions (Ca2+). Under normal cellular conditions, BKCa channel activation requires Ca2+ concentrations that typically occur in close proximity to Ca2+ sources. We show that BKCa channels affinity-purified from rat brain are assembled into macromolecular complexes with the voltage-gated calcium channels Cav1.2 (L-type), Cav2.1 (P/Q-type), and Cav2.2 (N-type). Heterologously expressed BKCa-Cav complexes reconstitute a functional "Ca2+ nanodomain" where Ca2+ influx through the Cav channel activates BKCa in the physiological voltage range with submillisecond kinetics. Complex formation with distinct Cav channels enables BKCa-mediated membrane hyperpolarization that controls neuronal firing pattern and release of hormones and transmitters in the central nervous system.


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