Regulation of mAChR Function and Expression

mAChR 功能和表达的调节

• 批准号: 7020719
• 负责人: DARRELL A JACKSON
• 金额: $ 22.89万
• 依托单位: UNIVERSITY OF MONTANA
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-03-15 至 2009-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7020719
• 关键词: SDS polyacrylamide gel electrophoresis; acetylcholine; autoradiography; cell line; gene expression; genetic transcription; hippocampus; hypoxia; immunoprecipitation; laboratory rat; muscarinic receptor; neurons; phosphorylation; receptor expression; tissue /cell culture; western blottings

DESCRIPTION (provided by applicant): It is estimated that in the United States 150,000 stroke-related deaths occur each year, making stroke the country's third-leading cause of death. In nonfatal strokes, ischemic injury to the hippocampus, a brain region known to be selectively vulnerable to ischemia, results in cognitive and memory impairment. After cerebral ischemia, surviving neurons undergo a variety of cellular responses that are not completely understood. The long-term goal of this research is to elucidate mechanisms of responses to cerebral ischemia. The present proposal focuses on one aspect of ischemia, hypoxia, and its effect on the fimctional expression of muscarinic acetylcholine receptors (mAChRs), which are thought to play a role in learning and memory. Our experiments will test the hypothesis that transient hypoxia causes a decrease in functional responsiveness of the m2 mAChRs and that the mechanism involved includes both pre- and post-translational modifications. Experiments are designed to determine the underlying mechanisms that mediate internalization, desensitization, and down-regulation of m2 mAChRs by transient hypoxia. The proposed study will use cultures of enriched primary hippocampal neurons and human embryonic kidney cells and mouse embryonic fibroblasts that stably express wild-type or mutated forms of the m2 mAChR. In Specific Aim 1, experiments will be performed to test the hypothesis that hypoxic insult induces phosphorylation of the m2 mAChR, thereby leading to internalization and decreased responsiveness to muscarinic agonists. In Specific Aim 2, experiments will be conducted to test the hypothesis that desensitization of the m2 mAChR by transient hypoxia is independent of m2 receptor internalization. In Specific Aim 3, experiments will be carried out to test the hypothesis that transient hypoxia decreases the expression of the m2 mAChR mRNA and/or protein. Together, these experiments will determine how hypoxia induces alterations in mAChR signaling and advance understanding of the consequences of stroke and transient ischemic attacks. Results from these studies will be useful in developing therapeutic interventions to reduce the impairment of learning and memory after ischemic insults.

描述（由申请人提供）：据估计，在美国每年发生150，000例与中风相关的死亡，使中风成为该国第三大死亡原因。在非致命性中风中，对海马体的缺血性损伤导致认知和记忆障碍，海马体是已知的选择性易受缺血影响的大脑区域。脑缺血后，存活的神经元经历了各种尚不完全清楚的细胞反应。本研究的长期目标是阐明脑缺血反应的机制。本研究的重点是缺血缺氧的一个方面，以及它对毒蕈碱型乙酰胆碱受体（mAChR）功能表达的影响，mAChR被认为在学习和记忆中起作用。我们的实验将测试的假设，即短暂缺氧引起的M2 mAChRs的功能反应性的降低，所涉及的机制包括翻译前和翻译后的修饰。实验的目的是确定潜在的机制，介导的内化，脱敏，和下调的m2 mAChRs的短暂缺氧。 拟议的研究将使用丰富的原代海马神经元和人胚肾细胞和小鼠胚胎成纤维细胞，稳定表达野生型或突变形式的m2 mAChR的文化。在具体目标1中，将进行实验以检验缺氧损伤诱导m2 mAChR磷酸化的假设，从而导致内化和对毒蕈碱激动剂的反应性降低。在具体目标2中，将进行实验以检验以下假设：瞬时缺氧对m2 mAChR的脱敏不依赖于m2受体内化。在具体目标3中，将进行实验以检验短暂缺氧降低m2 mAChR mRNA和/或蛋白表达的假设。总之，这些实验将确定缺氧如何诱导mAChR信号的改变，并促进对中风和短暂性脑缺血发作后果的理解。这些研究的结果将有助于开发治疗干预措施，以减少缺血性损伤后的学习和记忆障碍。