Dynamic ion selectivity of K2P channels and paradoxical depolarization

描述（由申请人提供）：在低钾血症或细胞外 K 水平降低的情况下，人类心肌细胞可能会发生矛盾的去极化，这与 K 的能斯特方程不一致。这种矛盾的去极化现象已经观察了三十多年。它对于低钾血症引起的心律失常的病因学也至关重要。然而，其分子机制尚不清楚。 K 通道的离子选择性通常被认为是静态的，不会随生理刺激而改变。 K 通道如何选择 K 而非其他单价阳离子仍然是一个未解决的问题。特别是，与四聚体 K 通道中的离子选择性和选择性过滤器相比，二聚体双孔域 K 通道 (K2P) 的离子选择性和选择性过滤器了解较少。我们的长期目标是了解 K 通道的生理作用和 K 通道功能的分子机制。本提案的目的是探索 TWIK-1（哺乳动物 K2P 通道的第一个克隆成员）在低钾血症中人类心肌细胞中的功能作用，并表征 K2P 通道的离子选择性和通透性的动态行为。基于过去三十年的研究、这些研究的意义以及我们对克隆的 TWIK-1 K 通道的初步研究，我们假设：1）TWIK-1 K 通道响应细胞外 K 水平降低的挑战，并通过改变离子选择性和传导内漏 Na 电流，导致低钾血症中人类心肌细胞的反极化； 2）K2P通道可以调节选择性过滤器的构象，并表现出离子选择性和单价阳离子渗透性的动态行为。通过采用离子通道和电生理学领域的标准方法和常规方法，我们将在两个具体目标中测试这些假设：1）研究TWIK-1 K通道如何在正常和低钾条件下调节人原代心肌细胞的静息电位和动作电位。 2) 研究在细胞内 K 不存在的情况下 K2P 通道对小碱金属离子和大有机单价阳离子的离子选择性和渗透性。拟议的研究将证明 TWIK-1 K 通道在人类心肌细胞中的生理作用，描述调节心脏兴奋性的新机制，为理解低钾血症中心脏的矛盾去极化提供新的见解，并阐明低钾血症引起的心律失常的病因学。它还将介绍生理条件下K通道动态离子选择性的概念，提供灵活的K通道选择性过滤器的证据，支持或补充有关K通道离子选择性的众所周知的假设，并提高对离子选择性和K2P通道选择性过滤器的理解。

DESCRIPTION (provided by applicant): In hypokalemia or lowered extracellular K+ levels, human cardiac cells can become paradoxically depolarized inconsistent with the Nernst equation for K+. Such paradoxical depolarization has been observed for over thirty years. It is also crucial to the etiology of hypokalemia-induced cardiac arrhythmia. However, its molecular mechanism is not well understood. Ion selectivity of K+ channels is generally considered to be static and not changed in response to physiological stimuli. How K+ channels select K+ over other monovalent cations still remains an unsolved question. Particularly, ion selectivity and the selectivity filter of dimeric two-pore domain K+ channels (K2P) are less understood compared to those in tetrameric K+ channels. Our long-term goal is to understand physiological roles of K+ channels and molecular mechanisms of K+ channel function. The objective of this proposal is to explore functional roles of TWIK-1, the first cloned member of mammalian K2P channels in human cardiomyocytes in hypokalemia, and to characterize dynamic behaviors in ion selectivity and permeability of K2P channels. Based on studies in the past thirty years, the implications that are derived from these studies, and our preliminary studies on cloned TWIK-1 K+ channels, we hypothesize: 1) TWIK-1 K+ channels respond to challenges of lowered extracellular K+ levels and contribute to paradoxical depolarization in human cardiomyocytes in hypokalemia by changing ion selectivity and conducting inward leak Na+ currents; 2) K2P channels can adjust the conformations of the selectivity filter and exhibit dynamic behaviors in ion selectivity and permeability for monovalent cations. By employing standard methods and conventional approaches in the field of ion channels and electrophysiology, we will test these hypotheses in two specific aims: 1) Investigate how TWIK-1 K+ channels regulate the resting potential and action potential of human primary cardiomyocytes in both normal and hypokalemic conditions. 2) Study ion selectivity and permeability of K2P channels for small alkali metal ions and large organic monovalent cations in the absence of intracellular K+. The proposed research will demonstrate physiological roles of TWIK-1 K+ channels in human cardiomyocytes, describe a novel mechanism that regulates cardiac excitability, provide novel insights on the understanding of paradoxical depolarization in the heart in hypokalemia, and shed light on the etiology of hypokalemia-induced cardiac arrhythmias. It will also introduce the concept of dynamic ion selectivity of K+ channels under physiological conditions, provide evidence of a flexible K+ selectivity filter, which supports or supplements well-known hypotheses regarding ion selectivity of K+ channels, and improve the understanding of ion selectivity and the selectivity filter of K2P channels.