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Mechanisms of benign neonatal familial convulsions

良性新生儿家族性惊厥的机制

基本信息

批准号：
7194363
负责人：
EDWARD C COOPER
金额：
$ 34.75万
依托单位：
UNIVERSITY OF PENNSYLVANIA
依托单位国家：
美国
项目类别：
财政年份：
2005
资助国家：
美国
起止时间：
2005-04-01 至 2010-03-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7194363
关键词：
Action Potentials Age Ankyrins Axon Behavioral Biological Biological Models Brain Cell Line Cells Condition Cultured Cells Dependence Development Disease Disruption Employee Strikes Epilepsy Exhibits Familial benign neonatal epilepsy Frequencies Genes Goals Hippocampus (Brain)Human Inborn Genetic Diseases Inherited Interneurons Ion Channel Lead Life Localized Location Maps Mediating Methods Missense Mutation Molecular Mus Mutant Strains Mice Mutation Myokymia Neonatal Neurologic Neurons Neurotransmitter Receptor Pain Pathway interactions Peripheral Peripheral Nerves Phenotype Physiological Play Potassium Channel Predisposition Presynaptic Terminals Proteins Ranvier&apos s Nodes Relative (related person)Research Personnel Risk Rodent Role Role playing therapy Scaffolding Protein Seizures Severities Signal Pathway Signal Transduction Site Syndrome System Testing Tetanus Helper Peptide Therapeutic Time Week Work deafness density design in vivo infancy insight mutant nervous system disorder neuron loss neuronal cell body neuronal excitability neurotransmission novel postnatal prevent programs protein protein interaction receptor research study septohippocampal therapeutic target tool voltage

项目摘要

DESCRIPTION (provided by applicant): Careful study of genes responsible for rare mendelian forms of human neurological disorders is a powerful approach for gaining insight into the causes, treatment, and potential cure for common, related diseases. The neuronal KCNQ genes were recently discovered as the result of the search for mutant genes causing Benign Familial Neonatal Convulsions, an autosomal dominant epileptic syndrome associated with seizures in infancy and throughout life. Mutations in neuronal KCNQ genes also result in myokymia (a peripheral nerve disorder) and deafness. The KCNQ genes encode subunits of voltage-dependent potassium channels. The long term goals of the proposed work is to understand the in vivo functions of these neuronal KCNQ channels, in order to better understand basic brain signaling mechanisms and to exploit these mechanisms for neurological therapeutics. KCNQ channels regulate neuronal excitability through their intrinsic, voltage-gated activity at particular locations in brain, and through their ability to serve as effectors for neurotransmitter receptors and intracellular signaling pathways. Determining specifically where KCNQ channels are localized in brain circuits, and how receptors, pathways and interacting proteins modulate their activity in the brain, will enhance our ability to exploit these channels as therapeutic targets in conditions involving excessive excitability or alterations and imbalances in modulatory neurotransmission, such as epilepsy and pain syndromes. The current proposal focuses on KCNQ channels on axons in hippocampus, where previous work by the investigator and others indicates KCNQ channels play important roles. It exploits newly available mutant mice with KCNQ2 mutations and phenotypes of increased seizure susceptibility and spontaneous seizures. The specific aims are to: (1) map the localization of KCNQ subunits in mammalian septohippocampal networks in developing and mature brain of normal and mutant rodents; (2) define the mechanisms targeting KCNQ subunits to axon initial segments and nodes of Ranvier; and (3) analyze the function of axonal KCNQ channels at the subcellular and cellular level.

描述(由申请人提供)：仔细研究导致罕见的孟德尔形式的人类神经疾病的基因是了解常见相关疾病的原因、治疗方法和潜在治疗方法的有力途径。神经元KCNQ基因是最近发现的，是寻找导致良性家族性新生儿惊厥的突变基因的结果，良性家族性新生儿惊厥是一种常染色体显性遗传性癫痫综合征，与婴儿期和终生癫痫发作有关。神经性KCNQ基因的突变也会导致肌痉挛(一种外周神经疾病)和耳聋。KCNQ基因编码电压依赖性钾通道的亚基。这项拟议工作的长期目标是了解这些神经元KCNQ通道在体内的功能，以便更好地了解基本的大脑信号机制，并将这些机制用于神经治疗。KCNQ通道通过其在大脑特定位置的固有电压门控活动，以及通过其作为神经递质受体和细胞内信号通路的效应器的能力来调节神经元的兴奋性。明确地确定KCNQ通道在大脑回路中的位置，以及受体、通路和相互作用的蛋白质如何调节它们在大脑中的活动，将增强我们在涉及过度兴奋或调制神经传递的改变和失衡的情况下作为治疗靶点的能力，如癫痫和疼痛综合征。目前的建议集中在海马区轴突上的KCNQ通道，研究人员等人之前的工作表明KCNQ通道在其中发挥着重要作用。它利用新获得的具有KCNQ2突变的突变小鼠，以及增加癫痫易感性和自发性癫痫的表型。本研究的具体目的是：(1)定位KCNQ亚基在正常和突变啮齿动物发育和成熟脑中的隔-海马区网络中的定位；(2)确定针对Ranvier轴突起始节段和节点的KCNQ亚基的靶向机制；(3)在亚细胞和细胞水平上分析轴突KCNQ通道的功能。