Cell Type Specific Control of Neuronal Signaling

神经元信号传导的细胞类型特异性控制

• 批准号: 7999125
• 负责人: Martilias Stephen Farrell
• 金额: $ 2.99万
• 依托单位: UNIV OF NORTH CAROLINA CHAPEL HILL
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-07-01 至 2013-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7999125
• 关键词: Affect; Animal Behavior; Brain; Corpus striatum structure; Cyclic AMP; Designer Drugs; Development; Disease; Drug Delivery Systems; FOS gene; Family; G Protein-Coupled Receptor Signaling; G-Protein-Coupled Receptors; GTP-Binding Proteins; Genetic; Lead; Ligands; Measures; Neurons; Obsessive-Compulsive Disorder; Parkinson Disease; Pharmaceutical Preparations; Phosphorylation; Physiological; Population; Scientist; Signal Pathway; Signal Transduction; Specificity; Transgenic Mice; Work; addiction; cell type; design; in vivo; insight; neuropsychiatry; public health relevance; receptor; small molecule; tool

DESCRIPTION (provided by applicant): Dysfunctional neuronal circuits are thought to be responsible for neuropsychiatric disorders, including obsessive-compulsive disorder, Parkinson's disease and addiction. G protein-coupled receptors (GPCRs) differentially modulate the activity of neuronal circuits by interacting with different G proteins, (e.g. Gs, Gi, and Gq-families), and these receptors are well-established drug targets. Distinct subpopulations of neurons comprising these circuits often express similar receptor subtypes, making it impossible to create drugs that selectively target receptors in specific circuits. In order to determine how receptors might modulate neuronal circuits, it is necessary to selectively activate GPCR signaling in a specific neuronal population in vivo. For the past two decades, efforts have been made to create tools to selectively manipulate GPCR signaling in distinct neuron populations - from small molecule ligands to genetic deletion - but these approaches have off-target effects. These off-target effects effectively eliminate the possibility to determine how GPCR signaling in a specific neuronal population affects circuitry function. A promising advancement to enable this specific manipulation is the development of the Designer Receptors Exclusively Activated by Designer Drug (DREADD) family of receptors. The objective of this proposal is to validate this recently created tool in vivo using a transgenic mouse expressing the Gs DREADD in a specific population of neurons in the striatum. Specific Aim 1 will validate the tool by determining whether the Gs DREADD activates canonical Gs signaling pathways by measuring cAMP accumulation, ERK1/2 phosphorylation, DARPP-32 phosphorylation, and c-Fos expression. Specific Aim 2 will validate the physiological relevance of the Gs DREADD-induced signaling by assessing its effects on animal behavior. The completion of this proposal will provide neuroscientists a powerful new tool to exclusively modulate GPCR signaling in specific neuronal populations. PUBLIC HEALTH RELEVANCE: To understand how drugs work in the brain, scientists need to be able to manipulate certain components of the brain in a very precise manner. This proposal will validate a new tool designed to provide an unprecedented level of specificity to scientists. Information gained using this tool will yield new insight into brain function and may lead to development of new drugs for treating neuropsychiatric diseases.

描述（由申请人提供）：神经元回路功能障碍被认为是神经精神疾病的原因，包括强迫症、帕金森病和成瘾。G蛋白偶联受体（GPCR）通过与不同的G蛋白（例如Gs、Gi和Gq家族）相互作用来差异地调节神经元回路的活性，并且这些受体是公认的药物靶标。组成这些回路的不同神经元亚群通常表达相似的受体亚型，这使得不可能创造出选择性靶向特定回路中受体的药物。为了确定受体如何调节神经元回路，有必要在体内选择性地激活特定神经元群体中的GPCR信号。在过去的二十年里，人们一直在努力创造工具来选择性地操纵不同神经元群体中的GPCR信号传导-从小分子配体到遗传缺失-但这些方法具有脱靶效应。这些脱靶效应有效地消除了确定特定神经元群体中的GPCR信号传导如何影响电路功能的可能性。一个有希望的进展，使这种特定的操纵是设计师受体的设计师药物（DREADD）家族的受体的开发。本提案的目的是验证这个最近创建的工具，在体内使用转基因小鼠表达的GS DREADD在纹状体的神经元的特定群体。具体目标1将通过测量cAMP积累、ERK 1/2磷酸化、DARPP-32磷酸化和c-Fos表达来确定Gs DREADD是否激活经典Gs信号通路来验证该工具。具体目标2将通过评估其对动物行为的影响来验证Gs DREADD诱导的信号传导的生理相关性。该提案的完成将为神经科学家提供一个强大的新工具，专门调节特定神经元群体中的GPCR信号。 公共卫生相关性：为了了解药物如何在大脑中发挥作用，科学家需要能够以非常精确的方式操纵大脑的某些组成部分。该提案将验证一种旨在为科学家提供前所未有的特异性水平的新工具。使用该工具获得的信息将产生对大脑功能的新见解，并可能导致治疗神经精神疾病的新药的开发。