首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Ultrastructural localization of active zone and synaptic vesicle proteins in a preassembled multi-vesicle transport aggregate.
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Ultrastructural localization of active zone and synaptic vesicle proteins in a preassembled multi-vesicle transport aggregate.

机译:预先组装的多囊泡转运聚集物中活性区和突触囊泡蛋白的超微结构定位。

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摘要

Although it has been suggested that presynaptic active zone (AZ) may be preassembled, it is still unclear which entities carry the various proteins to the AZ during synaptogenesis. Here, I propose that aggregates of dense core vesicles (DCV) and small clear vesicles in the axons of young rat hippocampal cultures are carriers containing preformed AZ and synaptic vesicle (SV) components on their way to developing synapses. The aggregates were positively labeled with antibodies against Bassoon and Piccolo (two AZ cytomatrix proteins), VAMP, SV2, synaptotagmin (three SV membrane proteins), and synapsin I (a SV-associated protein). Bassoon and Piccolo labeling were localized at dense material both in the aggregates and at the AZ. In addition to the SV at the synapses, the SV membrane proteins labeled the clear vesicles in the aggregate as well as many other SV-like and pleiomorphic vesicular structures in the axons, and synapsin I labeling was associated with the vesicles in the aggregates. In single sections, these axonal vesicle aggregates were approximately 0.22 by 0.13 microm in average dimensions and contain one to two DCV and five to six small clear vesicles. Serial sections confirmed that the aggregates were not synaptic junctions sectioned en face. Labeling intensities of Bassoon and Piccolo measured from serially sectioned transport aggregates and AZ were within range of each other, suggesting that one or a few aggregates, but not individual DCV, can carry sufficient Bassoon and Piccolo to form an AZ. The present findings provide the first ultrastructural evidence localizing various AZ and SV proteins in a preassembled multi-vesicle transport aggregate that has the potential to quickly form a functional active zone.
机译:尽管已经暗示可以预先组装突触前活性区(AZ),但仍不清楚在突触形成过程中哪些实体将各种蛋白质携带到AZ。在这里,我建议年轻大鼠海马培养的轴突中的密集核心囊泡(DCV)和小的透明囊泡的聚集体是载有预先形成的AZ和突触囊泡(SV)成分的突触载体。用针对巴松管和短笛(两个AZ细胞基质蛋白),VAMP,SV2,突触结合蛋白(三个SV膜蛋白)和突触蛋白I(一个与SV相关的蛋白)的抗体对聚集体进行阳性标记。巴松管和短笛标记位于聚集体和AZ中的致密物质上。除了突触处的SV外,SV膜蛋白还标记了聚集物中的透明囊泡以及轴突中的许多其他SV样和多形囊泡结构,突触素I标记与聚集物中的囊泡相关。在单个部分中,这些轴突囊泡聚集体的平均尺寸约为0.22 x 0.13微米,并包含一到两个DCV和五到六个小的透明囊泡。连续切片证实,聚集体不是面对面切开的突触连接。从连续切片的运输聚集体和AZ测得的Bassoon和Piccolo的标记强度在彼此的范围内,这表明一个或几个聚集体而不是单个DCV可以携带足够的Bassoon和Piccolo形成AZ。本研究结果提供了第一个超微结构证据,将各种AZ和SV蛋白定位在预组装的多囊泡运输聚集体中,该聚集体具有快速形成功能性活性区的潜力。

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