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突触前分化的分子机制

Molecular mechanisms of presynaptic differentiation.

作者信息

Jin Yishi, Garner Craig C

机构信息

Division of Biological Sciences, Section of Neurobiology, Howard Hughes Medical Institute, University of California, San Diego, La Jolla, California 92093, USA.

出版信息

Annu Rev Cell Dev Biol. 2008;24:237-62. doi: 10.1146/annurev.cellbio.23.090506.123417.

Abstract

Information processing in the nervous system relies on properly localized and organized synaptic structures at the correct locations. The formation of synapses is a long and intricate process involving multiple interrelated steps. Decades of research have identified a large number of molecular components of the presynaptic compartment. In addition to neurotransmitter-containing synaptic vesicles, presynaptic terminals are defined by cytoskeletal and membrane specializations that allow highly regulated exo- and endocytosis of synaptic vesicles and that maintain precise registration with postsynaptic targets. Functional studies at multiple levels have revealed complex interactions between the transport of vesicular intermediates, the presynaptic cytoskeleton, growth cone navigation, and synaptic targets. With the advent of finer anatomical, physiological, and molecular tools, great insights have been gained toward the mechanistic dissection of functionally redundant processes controlling the specificity and dynamics of synapses. This review highlights the recent findings pertaining to the cellular and molecular regulation of presynaptic differentiation.

摘要

神经系统中的信息处理依赖于在正确位置上恰当定位和组织的突触结构。突触的形成是一个漫长而复杂的过程,涉及多个相互关联的步骤。数十年来的研究已经确定了突触前区室的大量分子成分。除了含有神经递质的突触小泡外,突触前终末由细胞骨架和膜特化所定义,这些特化允许突触小泡进行高度调控的胞吐和胞吞作用,并与突触后靶点保持精确对齐。多个层面的功能研究揭示了囊泡中间体运输、突触前细胞骨架、生长锥导航和突触靶点之间复杂的相互作用。随着更精细的解剖学、生理学和分子工具的出现,人们对控制突触特异性和动力学的功能冗余过程的机制剖析有了更深入的了解。本综述重点介绍了与突触前分化的细胞和分子调控相关的最新发现。

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