Modulation of Olfactory Bulb Neuron Current Properties

嗅球神经元电流特性的调节

• 批准号: 7876706
• 负责人: DEBRA Ann FADOOL
• 金额: $ 27.55万
• 依托单位: FLORIDA STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1998
• 资助国家: 美国
• 起止时间: 1998-01-01 至 2014-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7876706
• 关键词: Action Potentials; Adaptor Signaling Protein; Affect; American; Axon; Behavior; Behavioral; Biochemical; Body Weight; Caloric Restriction; Cells; Chemistry; Code; Complex; Diabetes Mellitus; Diet; Discrimination; Down-Regulation; Drug Delivery Systems; Electrophysiology (science); Energy Metabolism; Fatty acid glycerol esters; Frequencies; Gated Ion Channel; Gene Targeting; Genetic Models; Glucose; Homeostasis; Hormones; Insulin; Insulin Receptor; Insulin Resistance; Investigation; Ion Channel; Knockout Mice; Ligands; Link; Mediating; Melanocortin 4 Receptor; Membrane Potentials; Metabolic Diseases; Molecular; Mus; Mutant Strains Mice; Neurodegenerative Disorders; Neurons; Non-Insulin-Dependent Diabetes Mellitus; Obesity; Odorant Receptors; Odors; Overweight; Phenotype; Phosphoric Monoester Hydrolases; Phosphotransferases; Physiological; Physiology; Plastics; Potassium; Potassium Channel; Process; Property; Protein Biochemistry; Proteins; Receptor Protein-Tyrosine Kinases; Regulation; Research; Resistance; Role; Scorpions; Sensory; Serum; Shapes; Signal Transduction; Signaling Protein; Stream; Surveys; Synapses; System; Toxin; Transgenic Mice; Weight; Weight Gain; Work; Workload; base; design; feeding; genetic regulatory protein; glucose transport; heart circulation; interdisciplinary approach; mouse model; neuron development; neuroregulation; novel; olfactory bulb; olfactory threshold; protein protein interaction; public health relevance; receptor; scaffold; ubiquitin ligase; voltage

Description (provided by applicant): Ion channels are a component of multiprotein scaffolds regulated by molecular protein-protein interactions to control electrical excitability of neurons and provide proper subcellular adjacencies to downstream cell signaling machinery. The work in this proposal will focus upon non-traditional roles of a voltage-gated ion channel (Kv1.3) predominantly expressed in mitral cell neurons of the olfactory bulb to understand the contribution of voltage-gated activity to olfactory coding. The recently uncovered, multifarious role for K channels - including energy homeostasis, axon targeting, and development of neuronal cytoarchitecture - is poorly understood. A multidisciplinary approach using transgenic mouse models (odorant receptor-tagged mice, Kv1.3-null mice, YFP mitral cell mice, and MC4R-null mice) to study Kv1.3 activity is proposed incorporating the METHODS of olfactory bulb electrophysiology, protein biochemistry, intranasal hormone/drug delivery, olfactory discrimination (behavior), systems physiology, and anatomical analysis of olfactory circuitry as a means for determining the mechanistic details and global physiological effects of neuromodulation of voltage-gated activity in the olfactory bulb. The SPECIFIC AIMS of this proposal are based on three HYPOTHESES: 1. Interactions with signaling proteins in the insulin receptor kinase/phosphatase cascade regulate Kv1.3 ion channel activity. 2. Voltage-gated activity from Kv1.3 ion channels modulates olfactory bulb mitral cell activity and olfactory acuity. 3. Gene-targeted deletions of Kv1.3 channel protein and the melanocortin 4 receptor will provide mechanistic details of how this potassium channel regulates energy homeostasis that modulates olfactory sensory ability via glucose utilization. The broad, long-term OBJECTIVE of this research is to elucidate how neuromodulation of voltage-gated ion channel activity can give rise to diverse functions in the olfactory system such as long-term plastic changes in synaptic efficacy, links to energy metabolism, or to fine tune the expression of odorant receptors and their central targets. Understanding the general principles of how ion channels are regulated by well defined molecules enriched in the olfactory system and involved in metabolic disorders (diabetes) and neurodegenerative diseases (Alzheimer's) and why gene-targeted deletion of Kv1.3 increases olfactory ability and induces resistance to weight gain, holds great translational promise as a target for increasing odor discrimination or lessening imbalance in energy homeostasis (obesity). PUBLIC HEALTH RELEVANCE: Sixty-five percent of Americans are overweight; unwanted weight gain induces an increased workload on the heart and circulation, increases insulin resistance, and precipitates type II Diabetes. This proposal is designed to elucidate the basic cellular mechanisms of how ion channels expressed in the olfactory bulb are involved in body weight and energy metabolism; is there a link between olfactory ability and obesity?

描述（由申请人提供）：离子通道是由分子蛋白质-蛋白质相互作用调节的多蛋白质支架的组分，以控制神经元的电兴奋性并为下游细胞信号传导机制提供适当的亚细胞邻接。本提案中的工作将集中在电压门控离子通道（Kv1.3）主要在嗅球的二尖瓣细胞神经元中表达的非传统作用，以了解电压门控活动对嗅觉编码的贡献。最近发现的K通道的多种作用-包括能量稳态，轴突靶向和神经元细胞结构的发展-知之甚少。使用转基因小鼠模型的多学科方法本研究拟采用嗅球电生理、蛋白质生化、鼻内激素/药物给药、嗅觉辨别等方法，对Kv1.3活性进行研究（行为）、系统生理学和嗅觉回路的解剖学分析作为用于确定嗅球中电压门控活动的神经调节的机制细节和整体生理效应的手段。本提案的具体目标基于三个假设：1。与胰岛素受体激酶/磷酸酶级联中的信号蛋白的相互作用调节Kv1.3离子通道活性。2. Kv1.3离子通道的电压门控活性调节嗅球二尖瓣细胞活性和嗅觉灵敏度。3. Kv1.3通道蛋白和黑皮质素4受体的基因靶向缺失将提供该钾通道如何调节能量稳态的机制细节，该能量稳态通过葡萄糖利用来调节嗅觉感觉能力。本研究的广泛、长期目标是阐明电压门控离子通道活性的神经调节如何在嗅觉系统中产生多种功能，例如突触功效的长期可塑性变化、与能量代谢的联系或微调气味受体及其中心靶点的表达。了解离子通道如何被嗅觉系统中丰富的明确分子调节并参与代谢紊乱的一般原理（糖尿病）和神经退行性疾病（阿尔茨海默氏症）以及为什么基因靶向缺失Kv1.3增加嗅觉能力并诱导对体重增加的抵抗力，作为增加气味辨别或减轻能量稳态失衡（肥胖）的靶点，具有很大的转化前景。公共卫生相关性：65%的美国人超重;不必要的体重增加会增加心脏和循环的工作量，增加胰岛素抵抗，并促使II型糖尿病。这个提议旨在阐明嗅球中表达的离子通道如何参与体重和能量代谢的基本细胞机制;嗅觉能力和肥胖之间是否存在联系？