Kv2.1 membrane corrals:Regulators of K+ channel function and trafficking

Kv2.1 膜畜栏：K 通道功能和运输的调节者

• 批准号: 7921746
• 负责人: Michael M. TAMKUN
• 金额: $ 42.32万
• 依托单位: COLORADO STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-18 至 2011-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7921746
• 关键词: Actins; Address; Apoptosis; Apoptotic; Attention; Axon; Binding; Biological Assay; Botulinum Toxins; Brain; Brain Hypoxia-Ischemia; Carbachol; Cardiovascular system; Cell physiology; Cell surface; Cells; Chemicals; Clathrin; Cystic Fibrosis; Cytoplasm; Cytoskeleton; DNA Sequence Rearrangement; Data; Defect; Diffuse; Diffusion; Disease; Electrodes; Electrophysiology (science); Endocrine system; Endocytosis; Epilepsy; Event; F-Actin; Figs - dietary; Glutamates; Health; Hippocampus (Brain); Human; Hyperactive behavior; Image; Injury; Ion Channel; Ion Channel Protein; Ischemia; Kv2.1 channel; Label; Life; Link; Location; Long QT Syndrome; Membrane; Modeling; Modification; Molecular; Monitor; Movement; Mus; Mutagenesis; Neurobiology; Neuronal Injury; Neurons; Pathway interactions; Peptides; Permeability; Play; Potassium Channel; Protein Isoforms; Protein Kinase; Proteins; Publishing; Quantum Dots; Regulation; Research; Retrieval; Role; SNAP receptor; Signaling Molecule; Site; Site-Directed Mutagenesis; Stimulus; Stroke; Structure; Surface; Testing; Time; base; cell growth regulation; cellular imaging; density; depression; human disease; improved; in vivo; inhibitor/antagonist; interdisciplinary approach; moesin; neuronal cell body; neuronal excitability; neurotransmitter release; programs; public health relevance; research study; response; response to injury; trafficking; voltage clamp

DESCRIPTION (provided by applicant): Tremendous advances in ion channel research have been made with respect to channel structure and function. However, there is a lack of information regarding how living cells process ion channel proteins in real time. Such information is important since rapid modulation of ion channel surface expression is likely to represent a central mechanism in the regulation of cellular electrical excitability. Human diseases have already been linked to ion channel localization and trafficking defects. The Kv2.1 delayed-rectifier K+ channel targets to unique cell surface clusters in hippocampal neurons. Since these structures are regulated in vivo by stimuli associated with neuronal injury, i.e. hypoxia, ischemia, and excess neurotransmitter release, these microdomains are likely to participate in the neuro-protective response during such insults. However, Kv2.1 also plays a role in apoptosis, with this Kv isoform providing the increased K+ permeability required for the completion of the apoptotic program in cortical neurons. These diverse functions mandate that Kv2.1 activity and trafficking be tightly regulated. Our overall hypothesis is that the Kv2.1 surface clusters are central in the regulation of both Kv2.1 trafficking and function. Thus, a better understanding of cluster function will improve our ability to manage stroke-related issues. By clustering these channels within a defined surface compartment that serves as a platform for both insertion and retrieval, the regulation of trafficking is more efficient than if the channel is homogenously distributed over the cell surface. In addition, our preliminary data suggest that channels within the surface clusters do not conduct K+ until released from these cell surface domains, suggesting that K+ current density is controlled by more than transport to the cell surface. The proposed research will employ a multidisciplinary approach utilizing live cell imaging, single channel detection/tracking, site-directed mutagenesis and electrophysiology. The three Specific Aims will test the hypotheses that 1) Kv2.1 clusters represent cell surface platforms for channel insertion and retrieval, 2) stimulus-induced modification of the cortical cytoskeleton causes immediate release from the cell surface cluster and 3) Kv2.1 surface clusters are cell surface storage sites containing non-conducting channel. This research will have implications far beyond neurobiology, for Kv2.1 is the most widely expressed Kv channel and is also physiologically important to the cardiovascular and endocrine systems. PUBLIC HEALTH RELEVANCE: The proposed research examines the localization of the Kv2.1 potassium channel in brain neurons. This localization is essential in the neuro-protective response to stroke injury and hyperactivity in the brain. Mice lacking the Kv2.1 channel are epileptic and hyper-excitable. Understanding the molecular mechanisms underlying Kv2.1 localization will enhance the treatment of stroke and epilepsy.

描述（申请人提供）：离子通道研究在通道结构和功能方面取得了巨大进展。然而，缺乏关于活细胞如何在真实的时间内处理离子通道蛋白的信息。这些信息是重要的，因为离子通道表面表达的快速调节可能代表细胞电兴奋性调节的中心机制。人类疾病已经与离子通道定位和运输缺陷有关。Kv2.1延迟整流钾通道靶向海马神经元中独特的细胞表面簇。由于这些结构在体内受到与神经元损伤相关的刺激（即缺氧、缺血和过量神经递质释放）的调节，因此这些微区可能在这种损伤期间参与神经保护反应。然而，Kv2.1也在细胞凋亡中发挥作用，该Kv亚型提供了完成皮质神经元凋亡程序所需的增加的K+渗透性。这些不同的职能要求Kv2.1活动和贩运受到严格管制。我们的总体假设是，Kv2.1表面簇是Kv2.1运输和功能调节的中心。因此，更好地了解群集功能将提高我们管理中风相关问题的能力。通过将这些通道聚集在限定的表面隔室内，该表面隔室用作插入和取回的平台，与通道均匀分布在细胞表面上相比，运输的调节更有效。此外，我们的初步数据表明，通道内的表面集群不进行K+，直到从这些细胞表面域释放，这表明K+电流密度是由超过运输到细胞表面控制。拟议的研究将采用多学科方法，利用活细胞成像，单通道检测/跟踪，定点诱变和电生理学。三个特定目的将检验以下假设：1）Kv2.1簇代表通道插入和回收的细胞表面平台，2）刺激诱导的皮质细胞骨架修饰导致从细胞表面簇立即释放，3）Kv2.1表面簇是含有非传导通道的细胞表面储存位点。这项研究的意义将远远超出神经生物学，因为Kv2.1是最广泛表达的Kv通道，对心血管和内分泌系统也具有重要的生理意义。 公共卫生相关性：拟议的研究检查了Kv2.1钾通道在脑神经元中的定位。这种定位在对脑中风损伤和过度活跃的神经保护反应中是必不可少的。缺乏Kv2.1通道的小鼠是癫痫和过度兴奋的。了解Kv2.1定位的分子机制将增强中风和癫痫的治疗。