钾通道亚基kv1.8 (Kcna10)对I型和II型前庭毛细胞独特的向外整流电导至关重要。

Hannah R Martin, Anna Lysakowski, Ruth Anne Eatock
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摘要

在羊膜动物中,头部运动和倾斜是由两种形态和生理截然不同的前庭毛细胞(hc)检测的。成熟的I型细胞表达一个大而非常不寻常的钾电导g K,L,激活负的静息电位,赋予非常负的静息电位和低的输入电阻,并增强了从I型细胞到其花端传入终端的不寻常的非量子传输。根据Shaker K通道家族中的kv1.8 (KCNA10)作为候选g K,L亚基的线索,我们比较了kv1.8缺失小鼠和同窝对照小鼠的毛细胞的全细胞电压依赖性电流。我们发现,kv1.8不仅对于g K,L也是必需的,而且对于II型hc的快速灭活和延迟整流电流也是必需的,这些电流激活到静息电位为正。三种kv1.8相关电导的不同性质可能反映了与其他kv1.4 (KCNA4)等kv1亚基的不同混合。在两种类型的kv1.8 -零hc中,剩余的向外整流电导包括kv7 (KCNQ)通道。电流箝位记录表明,在两种HC类型中,kv1.8相关的电导增加了电压响应的速度和阻尼。加速前庭受体电位和非量子传入传递的特征可能有助于稳定四足动物从水到陆地的运动。图形化的简介:
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The potassium channel subunit KV1.8 (Kcna10) is essential for the distinctive outwardly rectifying conductances of type I and II vestibular hair cells.

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, gK,L, 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 KV1.8 (KCNA10) in the Shaker K channel family as a candidate gK,L subunit, we compared whole-cell voltage-dependent currents from utricular hair cells of KV1.8-null mice and littermate controls. We found that KV1.8 is necessary not just for gK,L 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 KV1.8-dependent conductances may reflect different mixing with other KV subunits that are reported to be differentially expressed in type I and II HCs. In KV1.8-null HCs of both types, residual outwardly rectifying conductances include KV7 (KCNQ) channels. Current clamp records show that in both HC types, KV1.8-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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