PHARMACOLOGICAL REGULATION OF BASAL GANGLIA ENRICHED PHOSPHOPROTEIN

基底节富含磷酸蛋白的药理调节

• 批准号: 6111334
• 负责人: GRETCHEN L SNYDER
• 金额: $ 30.36万
• 依托单位: ROCKEFELLER UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-07-01 至 2000-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6111334
• 关键词: basal ganglia; biological signal transduction; casein kinase; cell line; dopamine; enzyme activity; gene targeting; genetically modified animals; human tissue; laboratory mouse; laboratory rat; phosphatase inhibitor; phosphoprotein phosphatase; phosphoproteins; phosphorylation; postmortem; protein kinase; psychopharmacology; schizophrenia; tissue /cell culture

This project will seek to examine protein phosphorylation pathways in the basal ganglia which mediate the actions of dopamine in normal and abnormal brain function. The pharmacological regulation of phosphoproteins enriched in the basal ganglia will be studied using intact cell preparations derived from basal ganglia structures of normal animals (e.g., neostriatal slices, primary neostriatal cell cultures, synaptosomes) or in immortalized cells which mimic various physiological properties of basal ganglia neurons. In addition, the regulation of these phosphoproteins under physiological conditions will be studied by administration of drugs to normal, intact animals and the subsequent analysis of the phosphorylated proteins in the brains of these animals. The goal of these studies is to identify first messenger and signal transduction pathways which play a significant role in regulating the function of basal ganglia phosphoproteins in the intact animal. Some of these studies will seek to identify signaling pathways which regulate phosphoproteins by using transgenic animals, which express mutagenized phosphoproteins, or genetically-altered animals, which are deficient in cell signaling molecules. Finally, the levels of phosphoproteins and associated signaling molecules will be measured in post-mortem brain tissue from normal individuals and patients with schizophrenia, in order to assess the possible involvement of phosphoproteins and their regulatory pathways in this dopamine-associated brain disorder. It is anticipated that these studies will provide an essential understanding of dopamine-mediated protein phosphorylation in the normal brain and the possible role of this process in dopamine-mediated motor and psychiatric disease.

该项目将试图研究蛋白质磷酸化途径， 基底神经节介导多巴胺的作用， 大脑功能异常药物调节 在基底神经节中富集的磷蛋白将使用 来自正常人基底神经节结构的完整细胞制备物 动物（例如，新纹状体切片，原代新纹状体细胞培养物， 突触体）或在模拟各种生理学的永生化细胞中 基底神经节神经元的特性。此外，这些监管 生理条件下的磷蛋白将被研究， 对正常、完整的动物给药， 分析这些动物大脑中的磷酸化蛋白质。 这些研究的目的是确定第一信使和信号 转导途径在调节细胞凋亡中起重要作用， 完整动物中基底神经节磷蛋白的功能。一些 这些研究将寻求确定调节细胞凋亡的信号通路， 通过使用转基因动物，其表达突变的磷蛋白， 磷蛋白，或基因改变的动物，这是缺乏 细胞信号分子最后，磷蛋白和 相关的信号分子将在死后的大脑中被测量 正常个体和精神分裂症患者的组织， 评估磷蛋白及其 多巴胺相关的脑部疾病的调节途径。是 预计这些研究将提供一个基本的理解， 多巴胺介导的蛋白质磷酸化在正常大脑和 这一过程在多巴胺介导的运动和精神疾病中的可能作用 疾病