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网格蛋白介导的突触内吞作用。

Clathrin-mediated endocytosis at synapses.

作者信息

Jung Nadja, Haucke Volker

机构信息

Department of Membrane Biochemistry, Institute of Chemistry & Biochemistry, Freie Universität Berlin, Takustrasse 6, 14195 Berlin, Germany.

出版信息

Traffic. 2007 Sep;8(9):1129-36. doi: 10.1111/j.1600-0854.2007.00595.x. Epub 2007 Jun 5.

Abstract

Neurons are communication specialists that convert electrical into chemical signals at specialized cell-cell junctions termed synapses. Arrival of an action potential triggers calcium-regulated exocytosis of neurotransmitter (NT) from small synaptic vesicles (SVs), which then diffuses across the synaptic cleft and binds to postsynaptic receptors to elicit specific changes within the postsynaptic cell. Endocytosis of pre- and postsynaptic membrane proteins including SV components and postsynaptic NT receptors is essential for the proper functioning of the synapse. During the past several years, we have witnessed enormous progress in our understanding of the mechanics of clathrin-mediated endocytosis (CME) and its role in regulating exo-endocytic vesicle cycling at synapses. Here we summarize the molecular machinery used for recognition of synaptic membrane protein cargo and its clathrin-dependent internalization, and describe the inventory of tools that can be used to monitor vesicle cycling at synapses or to inhibit CME in a stage-specific manner.

摘要

神经元是通讯专家,它们在称为突触的特殊细胞间连接处以将电信号转化为化学信号。动作电位的到来触发神经递质(NT)从小突触囊泡(SVs)中通过钙调节的胞吐作用释放,然后其扩散穿过突触间隙并与突触后受体结合,以引发突触后细胞内的特定变化。包括SV成分和突触后NT受体在内的突触前和突触后膜蛋白的内吞作用对于突触的正常功能至关重要。在过去几年中,我们见证了对网格蛋白介导的内吞作用(CME)机制及其在调节突触处外-内吞囊泡循环中作用的理解取得了巨大进展。在这里,我们总结了用于识别突触膜蛋白货物及其网格蛋白依赖性内化的分子机制,并描述了可用于监测突触处囊泡循环或以阶段特异性方式抑制CME的工具清单。

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