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Regulation of Motor Neurons by Postsynaptic Targets

Regulation of Motor Neurons by Postsynaptic Targets
突触后靶标对运动神经元的调节
批准号:
9724155
负责人:
Arlene Chiu
金额:
$33.12万
依托单位国家:
美国
项目类别:
Continuing grant
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-08-15 至 1999-07-31

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中文摘要
翻译
IBN-9724155 Pi:Chiu A成熟的神经系统之所以能发挥作用,很大程度上是因为在适当的神经元组之间建立并维持了正确的突触连接。虽然我们还不完全了解如何建立和维持适当的连接,但很明显,神经元网络需要神经细胞和它们的突触伙伴之间的双向通信。邱博士有初步证据表明,下游或突触后的靶子可以“说话”,并调节神经细胞的特征。她的实验室已经制造出一种标记,可以识别只在成熟运动神经元(直接控制骨骼肌收缩的专门神经细胞)中存在的分子。这种分子之所以有趣,有几个原因。首先,它是非常有选择性的,只在这一单一的细胞群体中被检测到,这表明该分子肯定在这类神经元的功能中发挥着重要作用。其次,它似乎发育得很晚,此时运动神经元正在建立它们与肌肉细胞的成年连接模式。第三,它的存在需要目标肌肉的积极反应。最后,当神经和肌肉之间的通讯中断时,这种分子就会丢失。总之,这些结果表明,当运动神经元与肌肉形成并保持活跃的突触接触时,它们获得了一种在任何其他细胞类型中都没有的独特分子。这些初步结果表明,当肌肉被激活时,它们向突触前(上游)神经元返回一个信号;然后这个逆行信号赋予只有运动神经元才有的生化特性。通过这种方式,突触后靶点可以调节其神经细胞的生化性质。赵博士现在将研究运动神经元和肌肉之间的通讯如何调节这种分子的水平,她将识别和描述这种新颖的运动神经元特有的分子,以了解它在发出信号和维持神经系统正常连接方面的可能功能。
英文摘要
IBN-9724155 PI: CHIU A mature nervous system functions in large part because correct synaptic connections are made and maintained between the appropriate groups of neurons. Although we do not fully understand how appropriate connections are established and maintained, it is clear that neuronal networks require bi-directional communication between nerve cells and their synaptic partners. Dr. Chiu has preliminary evidence that the downstream or post-synaptic target can "talk back" and regulate the characteristics of the innervating neuron. Her laboratory has produced a marker that recognizes a molecule found only in mature motor neurons (the specialized nerve cells that directly control the contraction of skeletal muscles). This molecule is interesting for several reasons. First, it is very selective and detected only in this single population of cells, suggesting that the molecule must play an important role in the function of this class of neuron. Second, it appears very late in development, at a time when motor neurons establish their adult pattern of connections with muscle cells. Third, its presence requires an active response from the target muscle. Finally, the molecule is lost when communication between nerve and muscle is disrupted. Together, these results demonstrate that when motor neurons form and maintain active synaptic contact with muscles, they acquire a unique molecule not found in any other cell type. These preliminary results suggest that when muscles are activated, they return a signal to the presynaptic (upstream) neuron; this retrograde signal then confers a biochemical property found only in motor neurons. In this manner, the post-synaptic target can regulate the biochemical nature of its innervating neurons. Dr. Chiu will now investigate how communication between motor neuron and muscle regulates the levels of this molecule, and she will identify and characterize this novel, motor neuron-specific molecule to understand its possible functions in signalling a nd maintaining the normal wiring of the nervous system.
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