Man H Y, Ju W, Ahmadian G, Wang Y T
Research Institute of Hospital for Sick Children, Department of Laboratory Medicine and Pathobiology, University of Toronto, Canada.
Cell Mol Life Sci. 2000 Oct;57(11):1526-34. doi: 10.1007/pl00000637.
Modification of ligand-gated receptor function at the postsynaptic domain is one of the most important mechanisms by which the efficacy of synaptic transmission in the nervous system is regulated. Traditionally, these types of modifications have been thought to be achieved mainly by altering the channel-gating properties or conductance of the receptors. However, recent evidence suggests that AMPA (alpha-amino-3-hydroxyl-5-methyl-4-isoxayolepropionic acid)-type ligand-gated glutamate receptors are continuously recycling between the plasma membrane and the intracellular compartments via vesicle-mediated plasma membrane insertion and clathrin-dependent endocytosis. Regulation of either receptor insertion or endocytosis results in a rapid change in the number of these receptors expressed on the plasma membrane surface and in the receptor-mediated responses, thereby playing an important role in mediating certain forms of synaptic plasticity. Thus, controlling the number of postsynaptic receptors by regulating the intracellular trafficking and plasma membrane expression of the postsynaptic receptors may be a common and important mechanism of synaptic plasticity in the mammalian central nervous system.
对突触后结构域配体门控受体功能的修饰是调节神经系统中突触传递效能的最重要机制之一。传统上,这类修饰主要被认为是通过改变受体的通道门控特性或电导来实现的。然而,最近的证据表明,α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)型配体门控谷氨酸受体通过囊泡介导的质膜插入和网格蛋白依赖性内吞作用在质膜和细胞内区室之间持续循环。对受体插入或内吞作用的调节会导致质膜表面表达的这些受体数量以及受体介导的反应迅速变化,从而在介导某些形式的突触可塑性中发挥重要作用。因此,通过调节突触后受体的细胞内运输和质膜表达来控制突触后受体的数量可能是哺乳动物中枢神经系统中突触可塑性的一种常见且重要的机制。