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在体神经元全细胞分析突触小泡前体运输。

In vivo neuron-wide analysis of synaptic vesicle precursor trafficking.

机构信息

Department of Biology, Howard Hughes Medical Institute, Stanford University, Stanford, CA,, USA.

出版信息

Traffic. 2014 Mar;15(3):273-91. doi: 10.1111/tra.12142. Epub 2014 Jan 13.

DOI:10.1111/tra.12142
PMID:24320232
Abstract

During synapse development, synaptic proteins must be targeted to sites of presynaptic release. Directed transport as well as local sequestration of synaptic vesicle precursors (SVPs), membranous organelles containing many synaptic proteins, might contribute to this process. Using neuron-wide time-lapse microscopy, we studied SVP dynamics in the DA9 motor neuron in Caenorhabditis elegans. SVP transport was highly dynamic and bi-directional throughout the entire neuron, including the dendrite. While SVP trafficking was anterogradely biased in axonal segments prior to the synaptic domain, directionality of SVP movement was stochastic in the dendrite and distal axon. Furthermore, frequency of movement and speed were variable between different compartments. These data provide evidence that SVP transport is differentially regulated in distinct neuronal domains. It also suggests that polarized SVP transport in concert with local vesicle capturing is necessary for accurate presynapse formation and maintenance. SVP trafficking analysis of two hypomorphs for UNC-104/KIF1A in combination with mathematical modeling identified directionality of movement, entry of SVPs into the axon as well as axonal speeds as the important determinants of steady-state SVP distributions. Furthermore, detailed dissection of speed distributions for wild-type and unc-104/kif1a mutant animals revealed an unexpected role for UNC-104/KIF1A in dendritic SVP trafficking.

摘要

在突触发育过程中,突触蛋白必须被靶向到突触前释放的部位。定向运输以及突触囊泡前体 (SVPs) 的局部隔离,SVPs 是包含许多突触蛋白的膜细胞器,可能有助于这个过程。使用神经元全时延时显微镜,我们研究了秀丽隐杆线虫 DA9 运动神经元中的 SVP 动力学。SVP 运输在整个神经元中高度动态且双向,包括树突。虽然 SVP 运输在突触前的轴突段以前向偏向为主,但 SVP 运动的方向性在树突和远端轴突中是随机的。此外,不同隔室之间的运动频率和速度都不同。这些数据提供了证据,表明 SVP 运输在不同的神经元区域受到不同的调节。它还表明,与局部囊泡捕获相结合的极化 SVP 运输对于准确的突触前形成和维持是必要的。UNC-104/KIF1A 的两个功能不全突变体的 SVP 运输分析与数学建模相结合,确定了运动的方向性、SVPs 进入轴突以及轴突速度是稳态 SVP 分布的重要决定因素。此外,对野生型和 unc-104/kif1a 突变体动物的速度分布进行详细剖析,揭示了 UNC-104/KIF1A 在树突状 SVP 运输中的意外作用。

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