Department of Cell Biology and Physiology, Washington University, Missouri, United States.
Department of Biomedical Engineering, Washington University, Missouri, United States.
Elife. 2018 Oct 15;7:e39440. doi: 10.7554/eLife.39440.
Synaptic vesicle fusion occurs at specialized release sites at the active zone. How refilling of release sites with new vesicles is regulated in central synapses remains poorly understood. Using nanoscale-resolution detection of individual release events in rat hippocampal synapses we found that inhibition of myosin V, the predominant vesicle-associated motor, strongly reduced refilling of the release sites during repetitive stimulation. Single-vesicle tracking revealed that recycling vesicles continuously shuttle between a plasma membrane pool and an inner pool. Vesicle retention at the membrane pool was regulated by neural activity in a myosin V dependent manner. Ultrastructural measurements of vesicle occupancy at the plasma membrane together with analyses of single-vesicle trajectories during vesicle shuttling between the pools suggest that myosin V acts as a vesicle tether at the plasma membrane, rather than a motor transporting vesicles to the release sites, or directly regulating vesicle exocytosis.
突触囊泡融合发生在活性区的特化释放位点。中央突触中,新囊泡如何重新填充释放位点仍知之甚少。通过纳米级分辨率检测大鼠海马突触中的单个释放事件,我们发现抑制肌球蛋白 V(主要的囊泡相关运动蛋白)会强烈减少重复刺激期间释放位点的再填充。单囊泡追踪显示,循环囊泡在质膜池和内池之间持续穿梭。膜池中的囊泡保留受肌球蛋白 V 依赖性的神经活动调节。质膜囊泡占据的超微结构测量以及在囊泡在池之间穿梭过程中单囊泡轨迹的分析表明,肌球蛋白 V 作为质膜上的囊泡系绳,而不是将囊泡运送到释放位点的运动蛋白,或者直接调节囊泡胞吐。