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突触小泡循环。

The synaptic vesicle cycle.

作者信息

Sudhof Thomas C

机构信息

Center for Basic Neuroscience, Department of Molecular Genetics, Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9111, USA.Thomas.

出版信息

Annu Rev Neurosci. 2004;27:509-47. doi: 10.1146/annurev.neuro.26.041002.131412.

Abstract

Neurotransmitter release is mediated by exocytosis of synaptic vesicles at the presynaptic active zone of nerve terminals. To support rapid and repeated rounds of release, synaptic vesicles undergo a trafficking cycle. The focal point of the vesicle cycle is Ca2+-triggered exocytosis that is followed by different routes of endocytosis and recycling. Recycling then leads to the docking and priming of the vesicles for another round of exo- and endocytosis. Recent studies have led to a better definition than previously available of how Ca2+ triggers exocytosis and how vesicles recycle. In particular, insight into how Munc18-1 collaborates with SNARE proteins in fusion, how the vesicular Ca2+ sensor synaptotagmin 1 triggers fast release, and how the vesicular Rab3 protein regulates release by binding to the active zone proteins RIM1 alpha and RIM2 alpha has advanced our understanding of neurotransmitter release. The present review attempts to relate these molecular data with physiological results in an emerging view of nerve terminals as macromolecular machines.

摘要

神经递质的释放是由神经末梢突触前活性区突触小泡的胞吐作用介导的。为了支持快速且重复的释放过程,突触小泡经历一个运输循环。小泡循环的焦点是Ca2+触发的胞吐作用,随后是不同的内吞作用和再循环途径。再循环进而导致小泡对接并引发新一轮的胞吐和内吞作用。最近的研究对Ca2+如何触发胞吐作用以及小泡如何再循环给出了比以往更清晰的定义。特别是,对Munc18-1如何与SNARE蛋白在融合过程中协作、小泡Ca2+传感器突触结合蛋白1如何触发快速释放以及小泡Rab3蛋白如何通过与活性区蛋白RIM1α和RIM2α结合来调节释放的深入了解,推动了我们对神经递质释放的认识。本综述试图在将神经末梢视为大分子机器的新观点下,将这些分子数据与生理学结果联系起来。

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