Slick and Slack Heteromers in Neuronal Excitability

神经元兴奋性中的光滑和松弛异聚物

• 批准号: 7546091
• 负责人: Jack Kronengold
• 金额: $ 5.13万
• 依托单位: YALE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-05-01 至 2011-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7546091
• 关键词: Action Potentials; Address; Auditory; Autistic Disorder; Belief; Binding Sites; Brain Stem; Brain region; Cell Nucleus; Cerebral Ischemia-Hypoxia; Chloride Ion; Chlorides; Class; Condition; Dependence; Electrophysiology (science); Epilepsy; Fire - disasters; Fragile X Syndrome; Frequencies; Genes; Hypersensitivity; Image; Kinetics; Knowledge; Lead; Medial; Messenger RNA; Molecular Biology Techniques; Motor; Neurons; Pattern; Physiological; Potassium Channel; Property; Proteins; Purpose; Role; Sensory; Slice; Sodium; Syndrome; System; Testing; Therapeutic Intervention; Time; Tuberous sclerosis protein complex; autistic behaviour; neuronal excitability; protein expression; research study; therapeutic target; trapezoid body; voltage

DESCRIPTION (provided by applicant): KNa channels are activated by intracellular sodium and show only weak voltage dependence. The two genes which encode these channels, Slack and Slick, show overlapping mRNA and protein expression in certain brain regions, most notably in the auditory and olfactory systems. Slack and Slick channels differ significantly in their activation kinetics and their sensitivity to intracellular chloride, ATP and PKC. The specific aims of this proposal will determine whether they form heteromeric channels which contribute to native KNa currents in principal auditory neurons of the medial nucleus of the trapezoid body (MNTB). This proposal will address three specific aims. Aim 1 will determine whether Slack and Slick form heteromeric channels in heterologous expression systems. In Aim 2 we will assess the role of Slick and Slack subunits in the native KNa current of principal neurons of the MNTB. Specifically, we will test the hypothesis that Slick and Slack current levels contribute to the temporal accuracy of different patterns of action potential firing at different stimulation frequencies. Aim 3 will study the physiological significance of PKC modulation of Slack and Slick in regulating the excitability of native neurons. Experiments in this proposal will use techniques of molecular biology, electrophysiology and Na+ imaging. The purpose of this proposal is to identify the role of KNa in auditory neurons and consequently increase our understanding of auditory network properties. It is our belief that this will lead to potential, therapeutic targets for pathological conditions such as are seen when auditory hypersensitivity gates stereotypic motor autistic behavior patterns. Furthering our understanding of normal sensory encoding could have far reaching implications towards our understanding of Autism and other overlapping conditions such as Fragile X syndrome, Reft syndrome and Tuberous sclerosis complex. In addition, advancing the knowledge of this unique class of channels will in all likelihood lead to therapeutic interventions due to their putative protective roles in hypoxia and cerebral ischemia. Moreover, their pharmacological activation would make them a target for control of epileptic seizure activity.

描述（由申请人提供）：KNa通道由细胞内钠激活，仅表现出微弱的电压依赖性。编码这些通道的两个基因，Slack和Slick，在大脑的某些区域，尤其是听觉和嗅觉系统中，显示出重叠的mRNA和蛋白质表达。松弛通道和光滑通道在激活动力学和对细胞内氯化物、ATP和PKC的敏感性方面存在显著差异。该提案的具体目的将确定它们是否形成异质通道，从而促进梯形体（MNTB）内侧核主要听觉神经元的天然KNa电流。这项建议将涉及三个具体目标。目的1将确定Slack和Slick是否在异源表达系统中形成异质通道。在Aim 2中，我们将评估Slick和Slack亚基在MNTB主要神经元的原生KNa电流中的作用。具体来说，我们将测试Slick和Slack电流水平对不同动作电位放电模式的时间准确性的影响