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神经元突触前可塑性的结构及分子基础
引用本文:潘平越,陆佩华,盛祖杭.神经元突触前可塑性的结构及分子基础[J].生物化学与生物物理进展,2004,31(7):584-589.
作者姓名:潘平越  陆佩华  盛祖杭
作者单位:1. 上海第二医科大学神经生物学实验室,上海,200025
2. 上海第二医科大学神经生物学实验室,上海,200025;Synaptic Function University National Institute of Neurological Disorders and Stroke National Institutes of Health Bethesda Maryland 20892 USA
基金项目:上海市科技发展基金资助项目(01JC14023).
摘    要:突触可塑性是神经元间信息传递的重要生理调控机制,它包括突触前可塑性和突触后可塑性.突触前可塑性是指通过对神经递质释放过程的干预、修饰,调节突触强度的过程.突触强度的变化,是通过影响量子的大小,活动区的个数和囊泡释放概率来实现的.而突触前囊泡活动尤为重要:从转运、搭靠、融合至内吞进入下一轮循环,每一步都是由一群互相作用的蛋白质共同完成的.

关 键 词:突触前可塑性,突触强度,量子大小,活动区,递质释放概率
收稿时间:1/5/2004 12:00:00 AM
修稿时间:2004/2/28 0:00:00

The Structural and Molecular Mechanism of Neuronal Presynaptic Plasticity
PAN Ping-Yue,LU Pei-Hua and SHENG Zu-Hang.The Structural and Molecular Mechanism of Neuronal Presynaptic Plasticity[J].Progress In Biochemistry and Biophysics,2004,31(7):584-589.
Authors:PAN Ping-Yue  LU Pei-Hua and SHENG Zu-Hang
Institution:Department of Neurobiology, Shanghai Second Medical University, Shanghai 200025, China;Department of Neurobiology, Shanghai Second Medical University, Shanghai 200025, China;Department of Neurobiology, Shanghai Second Medical University, Shanghai 200025, China;Synaptic Function University, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, USA
Abstract:Synaptic plasticity is a physiologically important mechanism underlying neuronal information processing. In terms of expression site, synaptic plasticity can be divided into presynaptic and postsynaptic. Presynaptic plasticity is implicated in the modulation of the neurotransmitter release machinery and consequently in synaptic strength. From a physiological perspective, this type of plasticity could be derived from a change in quantal size, active zone structure, probability of transmitter release, especially, synaptic vesicle dynamics: from synaptic vesicle trafficking to the nerve terminal, docking at or fusion with the presynaptic plasma membrane, and finally, reconstitution following endocytosis. Each of these steps is mediated by the concerted activities of multiple proteins and protein complexes, thus presenting numerous points at which the cascades leading to effective neurotransmitter release could be modulated. Potential mechanisms by which the synaptic vesicle release could be modulated and synaptic activity could be silenced or enhanced at the presynaptic terminal are reviewed.
Keywords:presynaptic plasticity  synaptic strength  quantal size  active zone  probability of transmitter release
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