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Regulation of the Synaptic Localization of the nAChR

nAChR 突触定位的调节

基本信息

批准号：
7248693
负责人：
MICHAEL J FERNS
金额：
$ 29.08万
依托单位：
UNIVERSITY OF CALIFORNIA AT DAVIS
依托单位国家：
美国
项目类别：
财政年份：
2004
资助国家：
美国
起止时间：
2004-07-01 至 2009-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7248693
关键词：
Agrin Antibodies Autoimmune myasthenic syndromes Binding Binding Sites COS Cells Chemical Synapse Chimera organism Cholinergic Receptors Chromosome Pairing Collaborations Complex Cytoskeleton Gated Ion Channel Genes Goals Ligands Link Localized Maintenance Maps Mediating Membrane Metabolic Molecular Motor Neurons Muscle Muscle Cells Muscle Weakness Muscle-Specific Kinase Mutate Mutation Myasthenic Syndrome Nerve Neuromuscular Diseases Neuromuscular Junction Neurotransmitter Receptor Patients Pattern Phosphorylation Phosphorylation Site Play Postsynaptic Membrane Process Regulation Role Scaffolding Protein Signal Transduction Site Synapses Synaptic Transmission Testing Transgenic Mice Tyrosine Tyrosine Phosphorylation Vertebrates Work agrin receptor density in vivo peripheral membrane protein 43K postsynaptic presynaptic receptor research study synaptic function synaptogenesis

项目摘要

DESCRIPTION (provided by applicant): Synapses are highly specialized for efficient synaptic transmission, with the transmitter release sites in the presynaptic nerve terminal being aligned with postsynaptic concentrations of the neurotransmitter receptor. At the developing neuromuscular junction, a nerve-derived factor called agrin directs the postsynaptic localization of the acetylcholine receptor, and our goal is to understand the molecular mechanisms that underlie agrin's action. Specifically, we will test the hypothesis that agrin regulates AChR localization by inducing phosphorylation of the AChR and altering its association with the intracellular scaffolding protein, rapsyn. We have the following specific aims: (1) To define the role of agrin-induced phosphoryation of the beta subunit in AChR localization. We will generate transgenic mice with a beta subunit lacking the phosphorylation site, and then determine whether this mutation impairs the synaptic localization of the AChR. We will also determine whether phosphorylation specifically regulates the anchoring, clustering, and/or stabilization of the receptor in the postsynaptic membrane. (2) To define the molecular mechanism of rapsyn-mediated AChR localization. Here, we will define rapsyn's binding site(s) on the AChR and determine whether binding is regulated by agrin. Moreover, we will investigate how agrin-induced changes in rapsyn/AChR association mediate receptor localization. This work is directly relevant to neuromuscular disorders such as congenital and autoimmune myasthenic syndromes, where there are severe deficiencies in AChR levels at the synapse, leading to impaired synaptic function and debilitating muscle weakness. Our work will help define the mechanisms involved in receptor localization and may suggest strategies to stabilize its localization in patients with myasthenic syndromes or other forms of neuromuscular disease.

描述（由申请人提供）：突触是高度专门化的高效突触传递，突触前神经终端的递质释放位点与突触后神经递质受体的浓度一致。在发育中的神经肌肉连接处，一种叫做agrin的神经衍生因子指导乙酰胆碱受体的突触后定位，我们的目标是了解agrin作用背后的分子机制。具体来说，我们将验证agin通过诱导AChR磷酸化并改变其与细胞内支架蛋白rapsyn的关联来调节AChR定位的假设。我们有以下具体目的：(1)确定农用蛋白诱导的β亚基磷酸化在AChR定位中的作用。我们将产生具有缺乏磷酸化位点的β亚基的转基因小鼠，然后确定该突变是否会损害AChR的突触定位。我们还将确定磷酸化是否特异性调节突触后膜中受体的锚定、聚集和/或稳定。(2)明确rapsyn介导的AChR定位的分子机制。在这里，我们将定义rapsyn在AChR上的结合位点，并确定结合是否受agrin的调节。此外，我们将研究agrin诱导的rapsyn/AChR关联变化如何介导受体定位。这项工作与先天性和自身免疫性肌无力综合征等神经肌肉疾病直接相关，其中突触AChR水平严重不足，导致突触功能受损和衰弱性肌肉无力。我们的工作将有助于确定受体定位的机制，并可能建议在肌无力综合征或其他形式的神经肌肉疾病患者中稳定其定位的策略。