ION CHANNEL REGULATION AND MODULATION IN CARDIAC MUSCLE

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 在哺乳动物心肌中发现了多种类型的电压门控钾离子通道，它们具有不同的时间和电压依赖性以及药理学敏感性。这种多样性具有生理意义，因为各种Kv通道在控制动作电位波形和不应性中发挥不同的作用。虽然在识别Kv通道成孔（？）编码不同心脏Kv通道的亚基，Kv通道辅助亚基（minK/ MiRPs，Kv？，KChAP，KChIP，DPPX）的理解相当有限。异源表达系统的研究表明，KV附件亚基可以调节各种KV？亚基编码的通道，并且每种类型的Kv通道可能由多个附属亚基调制。其他最近的研究表明，心脏Kv（和其他）通道作为大分子蛋白质复合物的组成部分，包括孔形成和辅助亚基，以及影响通道特性和介导与肌动蛋白细胞骨架和细胞外基质相互作用的其他调节蛋白。去定义千伏的生理作用？1、KChIP 2和DPP 6亚基，本文提出的研究将直接探测这些亚基在完整的心脏（小鼠心室）肌细胞中产生天然Kv通道Ito、f、Ito、s、IK、slow和Iss中的功能。将在体内和体外操纵辅助亚基的表达水平或性质，并且将直接（并且同时）确定这些操纵对心肌Ito、f、Ito、s、IK、slow和Iss的性质和细胞表面表达的功能后果。拟议的研究将揭示单个Kv通道类型是否受多个Kv辅助亚基的调节/调制。此外，这些研究将允许直接测试Kv辅助亚基是多功能的，调节/调节多种类型的（Kv a亚基编码的）心脏Kv通道的功能的假设。我们预计，这些研究将提供从根本上重要的心脏Kv通道大分子复合物的动态调节的Kv通道辅助亚基的作用的新见解。

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Multiple types of voltage-gated K+ (Kv) channels with distinct time- and voltage-dependent properties and pharmacological sensitivities have been identified in the mammalian myocardium. This diversity has a physiological significance in that the various Kv channels play distinct roles in controlling action potential waveforms and refractoriness. Although considerable progress has been made in identifying the Kv channel pore-forming (?) subunits that encode diverse cardiac Kv channels, the functional roles of the Kv channel accessory subunits (minK/ MiRPs, Kv?, KChAP, KChIP, DPPX) are rather poorly understood. Studies in heterologous expression systems suggest that Kv accessory subunits can modulate the properties of a variety of Kv ? subunit encoded channels and that each type of Kv channel likely is modulated by multiple accessory subunits. Other recent studies suggest that cardiac Kv (and other) channels function as components of macromolecular protein complexes, comprising pore-forming and accessory subunits, as well as additional regulatory proteins that influence channel properties and mediate interactions with the actin cytoskeleton and the extracellular matrix. To define the physiological roles of the Kv?1, KChlP2 and DPP6 subunits, the studies proposed here will probe directly the functioning of these subunits in the generation of the native Kv channels, lto,f, Ito.s, IK,slow and Iss, in intact cardiac (mouse ventricular) myocytes. The expression levels or the properties of the accessory subunits will be manipulated in vivo and in vitro, and the functional consequences of these manipulations on the properties and cell surface expression of myocardial lto,f, Ito.s, IK,slow and Iss will be determined directly (and simultaneously). The proposed studies will reveal whether individual Kv channel types are regulated/modulated by multiple Kv accessory subunits. In addition, these studies will allow direct testing of the hypothesis that Kv accessory subunits are multifunctional, regulating/modulating the functioning of multiple types of (Kv a subunit encoded) cardiac Kv channels. We anticipate that these studies will provide fundamentally important new insights into the role of Kv channel accessory subunits in the dynamic regulation of cardiac Kv channel macromolecular complexes.