D2 Receptor Induced Sensitization of Adenylate Cyclase

D2 受体诱导的腺苷酸环化酶致敏

• 批准号: 8107335
• 负责人: Carmen W. Dessauer
• 金额: $ 40.61万
• 依托单位: PURDUE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-05-10 至 2013-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8107335
• 关键词: Acute; Address; Adenosine; Adenylate Cyclase; Alzheimer' s Disease; Animal Model; Biochemical; Biological Assay; Cell model; Cells; Chemicals; Chronic; Corpus striatum structure; Cyclic AMP; DNA Sequence Rearrangement; Development; Disease; Dissociation; Dopamine; Dopamine D2 Receptor; Dopamine Receptor; Drug Delivery Systems; Drug abuse; Drug usage; Event; Fluorescence; Future; G Protein-Coupled Receptor Genes; G-Protein-Coupled Receptors; GTP-Binding Proteins; Goals; In Vitro; Individual; Lead; Life; Mental Depression; Methodological Studies; Modeling; Molecular; Muscarinic Acetylcholine Receptor; Muscarinics; Names; Neurons; Opioid; Opioid Receptor; Outcome; Pain; Parkinson Disease; Pertussis Toxin; Pharmaceutical Preparations; Protein Isoforms; Protein Subunits; Proteins; Reagent; Receptor Activation; Receptor Signaling; Research; Research Proposals; Role; Schizophrenia; Screening procedure; Series; Serotonin; Signal Transduction; Specificity; Staging; Technology; Testing; base; cDNA Library; design; dopamine D2L receptor; drug of abuse; in vivo; inhibitor/antagonist; innovation; insight; mutant; nervous system disorder; neuropsychiatry; novel; prevent; protein protein interaction; receptor; receptor coupling; research study; response; serotonin receptor; small hairpin RNA; small molecule; tool

DESCRIPTION (provided by applicant): D2 dopamine receptors have been implicated in neuropsychiatric and neurologic disorders including schizophrenia, drug abuse, and Parkinson's disease. Acute activation of D2 dopamine receptors inhibits cyclic AMP accumulation; however, persistent activation of D2 dopamine receptors enhances subsequent drug-stimulated cyclic AMP accumulation. This heterologous sensitization of adenylyl cyclase (AC) signaling occurs following persistent activation of several G?i/o-coupled receptors in vitro and in vivo. The overall objective of this research proposal is to elucidate the molecular mechanisms involved in heterologous sensitization of AC following persistent activation of D2-like dopamine receptors. Previous studies support a hypothesis that heterologous sensitization requires the activation of G?i/o subunits to induce sensitization through a G??-dependent mechanism. We hypothesize that G?? subunits lead to heterologous sensitization of individual AC isoforms through both direct and indirect mechanisms. The indirect mechanisms may involve protein-protein interactions as well as G?s. The general approach for these studies will be to express heterologously D2L dopamine receptors together with well characterized wild-type or mutant ACs (e.g. AC1, AC2, and AC5) for intact cell experiments in unique cellular backgrounds (i.e., G protein subunit deficient). This strategy takes advantage of recently discovered molecular and cellular tools to study G protein signaling as well as novel fluorescent technologies. The first specific aim will test the hypothesis that heterologous sensitization of select isoforms of AC involves G??-AC interactions and requires G?? subunit signaling. These studies will use a series of AC mutants, unique cellular models, small molecule inhibitors of G?? subunit signaling, and striatal neurons. The second specific aim will determine the roles and requirements for G protein subunits in modulating receptor-AC and AC-AC interactions. These experiments will use bimolecular fluorescence complementation (BiFC) to probe the specific role of G?? and G?s subunits in modulating basal and drug-induced protein-protein interactions in living cells. The third specific aim will identify and characterize the AC "sensitization interactome" using BiFC in a neuronal cell model. These studies will use BiFC to perform cDNA library screening to identify sensitization-induced interacting proteins of AC in living cells. Completion of the proposed studies will deliver mechanistic information regarding specific G protein subunits and new protein targets that could ultimately be used to prevent the development and expression of heterologous sensitization in vivo. PUBLIC HEALTH RELEVANCE: Understanding the molecular mechanisms responsible for D2 dopamine receptor-induced sensitization of adenylyl cyclase has implications in a variety of diseases including schizophrenia, Parkinson's disease, and drug abuse. Sensitization of adenylyl cyclase signaling occurs following persistent activation of several G?i/o-coupled receptors. Thus, the information discovered here is also relevant to many G protein-coupled receptors that are targets of drugs used to treat pain, depression, and Alzheimer's disease (e.g., opioid, serotonin, and muscarinic receptors).

描述（由申请人提供）：D2多巴胺受体与神经精神和神经系统疾病有关，包括精神分裂症、药物滥用和帕金森病。D2多巴胺受体的急性激活抑制环AMP蓄积;然而，D2多巴胺受体的持续激活增强随后的药物刺激的环AMP蓄积。这种异源的腺苷酸环化酶（AC）信号转导的敏化发生后，持续激活几个G？I/O偶联受体的体外和体内研究。本研究的总体目标是阐明D2样多巴胺受体持续激活后AC异源致敏的分子机制。以前的研究支持一个假设，即异源致敏需要激活G？i/o亚基通过G？？-诱导致敏依赖机制我们假设G？亚基通过直接和间接机制导致个体AC同种型的异源致敏。间接机制可能涉及蛋白质-蛋白质相互作用以及G？S.这些研究的一般方法将是表达异源D2 L多巴胺受体以及充分表征的野生型或突变AC（例如AC 1、AC 2和AC 5），用于独特细胞背景（即，G蛋白亚基缺陷）。该策略利用最近发现的分子和细胞工具来研究G蛋白信号传导以及新的荧光技术。第一个具体目标将测试AC选择亚型的异源致敏涉及G？？-的假设AC相互作用，需要G？？亚基信号这些研究将使用一系列AC突变体，独特的细胞模型，小分子G？？亚基信号和纹状体神经元。第二个具体目标将确定G蛋白亚基在调节受体-AC和AC-AC相互作用中的作用和要求。这些实验将使用双分子荧光互补（BiFC）探测G？？而G？s亚基在调节基础和药物诱导的蛋白质-蛋白质相互作用的活细胞。第三个具体目标是在神经元细胞模型中使用BiFC识别和表征AC“致敏相互作用组”。这些研究将使用BiFC进行cDNA文库筛选，以鉴定活细胞中AC致敏诱导的相互作用蛋白。完成拟议的研究将提供有关特定G蛋白亚基和新蛋白靶点的机制信息，这些信息最终可用于防止体内异源致敏的发展和表达。 公共卫生相关性：了解负责D2多巴胺受体诱导的腺苷酸环化酶致敏的分子机制在包括精神分裂症、帕金森病和药物滥用在内的多种疾病中具有意义。腺苷酸环化酶信号的敏化发生后，持续激活几个G？I/O偶联受体。因此，这里发现的信息也与许多G蛋白偶联受体有关，这些受体是用于治疗疼痛、抑郁和阿尔茨海默病的药物的靶点（例如，阿片样物质、5-羟色胺和毒蕈碱受体）。