Formation of Neuronal Cholinergic Synapses
Formation of Neuronal Cholinergic Synapses
批准号:
6756513
负责人:
Guoping Feng
金额:
$32.92万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-06-01 至 2007-05-31
关键词:
Xenopus oocytebiological signal transductioncell linecentral nervous systemgene targetinggenetically modified animalsin situ hybridizationlaboratory mouseneuronsneuroregulationnicotinic receptorsperipheral nervous systemprotein bindingprotein isoformsprotein protein interactionprotein structure functionreceptor bindingsuperior cervical ganglionsynaptogenesistissue /cell culturetransfection
中文摘要
描述(由申请人提供):精确的突触连接对于神经系统的正常功能至关重要。然而,令人惊讶的是,我们对体内调节神经元突触形成的机制知之甚少。本应用拟以小鼠颈上神经节(SCG)中简单易接近的外周突触为模型系统,研究神经元间突触的形成。本研究的重点是确定调节神经元胆碱能突触突触后装置组装的关键分子机制。神经元胆碱能系统在周围神经系统和中枢神经系统中都起着至关重要的作用。胆碱能功能的改变与几种神经系统疾病有关,包括阿尔茨海默病和精神分裂症。目前,调控神经元胆碱能突触形成、成熟和稳定的机制尚不清楚。在这里,我们建议使用分子和遗传方法来阐明调节神经元胆碱能突触突触后复合物组装的机制。第一个目标是确定神经元胆碱能突触突触后信号复合物的分子成分,并了解突触后信号复合物是如何组装的。第二个目的是确定靶向/锚定神经元烟碱乙酰胆碱受体到突触的分子机制。最后,我们将使用突变小鼠来测试我们已经在SCG突触中发现的一种突触后信号复合体蛋白的体内功能,并评估突触后信号复合体在神经元胆碱能突触的形成、成熟和稳定性中的重要性。这些研究将促进我们对神经系统中突触连接是如何建立和调节的理解。
英文摘要
DESCRIPTION (provided by applicant): Precise synaptic connectivity is essential for the proper function of the nervous system. Surprisingly, however, we know very little about mechanisms that regulate the formation of neuron-neuron synapses in vivo. This application proposes to use the simple and accessible peripheral synapse in the mouse superior cervical ganglion (SCG) as a model system to study the formation of neuron-neuron synapses. The focus of this proposed research is to determine key molecular mechanisms that regulate the assembly of the postsynaptic apparatus at neuronal cholinergic synapses. Neuronal cholinergic systems play critical roles in both the peripheral and central nervous systems. Alterations in cholinergic function have been implicated in several neurological disorders, including Alzheimer' s disease and schizophrenia. Currently, mechanisms regulating the formation, maturation and stability of neuronal cholinergic synapses are completely unknown. Here, we propose to use molecular and genetic approaches to elucidate the mechanisms that regulate the assembly of the postsynaptic complex at neuronal cholinergic synapses. The first aim is to identify the molecular components of the postsynaptic signaling complex at neuronal cholinergic synapses and to understand how the postsynaptic signaling complex is assembled. The second aim is to determine the molecular mechanisms that target/anchor neuronal nicotinic acetylcholine receptors to synapses. Finally, we will use mutant mice to test the in vivo function of one postsynaptic signaling complex protein we already identified at the SCG synapse and assess the importance of the postsynaptic signaling complex in the formation, maturation and stability of neuronal cholinergic synapses. These studies will advance our understanding of how the precise synaptic connectivity in the nervous system is established and regulated.
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