The potassium channel subunit K<sub>V</sub>1.8 (<i>Kcna10</i>) is essential for the distinctive outwardly rectifying conductances of type I and II vestibular hair cells.

Martin, Hannah R; Lysakowski, Anna; Eatock, Ruth Anne · Elife · 2024

basic_science · Level V

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Abstract

In amniotes, head motions and tilt are detected by two types of vestibular hair cells (HCs) with strikingly different morphology and physiology. Mature type I HCs express a large and very unusual potassium conductance, g<sub>K,L</sub>, which activates negative to resting potential, confers very negative resting potentials and low input resistances, and enhances an unusual non-quantal transmission from type I cells onto their calyceal afferent terminals. Following clues pointing to K<sub>V</sub>1.8 (<i>Kcna10</i>) in the Shaker K channel family as a candidate g<sub>K,L</sub> subunit, we compared whole-cell voltage-dependent currents from utricular HCs of K<sub>V</sub>1.8-null mice and littermate controls. We found that K<sub>V</sub>1.8 is necessary not just for g<sub>K,L</sub> but also for fast-inactivating and delayed rectifier currents in type II HCs, which activate positive to resting potential. The distinct properties of the three K<sub>V</sub>1.8-dependent conductances may reflect different mixing with other K<sub>V</sub> subunits that are reported to be differentially expressed in type I and II HCs. In K<sub>V</sub>1.8-null HCs of both types, residual outwardly rectifying conductances include K<sub>V</sub>7 (<i>Knq</i>) channels. Current clamp records show that in both HC types, K<sub>V</sub>1.8-dependent conductances increase the speed and damping of voltage responses. Features that speed up vestibular receptor potentials and non-quantal afferent transmission may have helped stabilize locomotion as tetrapods moved from water to land.

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