Transient docking of synaptic vesicles: Implications and mechanisms

被引:16
|
作者
Kusick, Grant F. [1 ,2 ]
Ogunmowo, Tyler H. [1 ,2 ]
Watanabe, Shigeki [1 ,3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Cell Biol, 725 N Wolfe St, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Biochem Cellular & Mol Biol Grad Program, 1830 E Monument St, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ, Sch Med, Solomon H Snyder Dept Neurosci, 725 N Wolfe St, Baltimore, MD 21287 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
READILY RELEASABLE POOL; SYNAPTOTAGMIN; 7; TRANSMITTER RELEASE; QUANTITATIVE-ANALYSIS; ASYNCHRONOUS RELEASE; CA2+ SENSOR; CALCIUM; TRANSMISSION; FUSION; AUGMENTATION;
D O I
10.1016/j.conb.2022.102535
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
As synaptic vesicles fuse, they must continually be replaced with new docked, fusion-competent vesicles to sustain neurotransmission. It has long been appreciated that vesicles are recruited to docking sites in an activity-dependent manner. However, once entering the sites, vesicles were thought to be stably docked, awaiting calcium signals. Based on recent data from electrophysiology, electron microscopy, biochemistry, and computer simulations, a picture emerges in which vesicles can rapidly and reversibly transit between docking and undocking during activity. This "transient docking" can account for many aspects of synaptic physiology. In this review, we cover recent evidence for transient docking, physiological processes at the synapse that it may support, and progress on the underlying mechanisms. We also discuss an open question: what determines for how long and whether vesicles stay docked, or eventually undock?
引用
收藏
页数:10
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