Tao-Cheng J-H
NINDS EM Facility, NIH, Building 49, Room 3A50, Bethesda, MD 20892-4477, USA.
Neuroscience. 2007 Dec 12;150(3):575-84. doi: 10.1016/j.neuroscience.2007.09.031. Epub 2007 Sep 19.
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.
尽管有人提出突触前活性区(AZ)可能是预先组装好的,但在突触形成过程中,究竟是哪些实体将各种蛋白质运送到AZ仍不清楚。在此,我提出,在幼鼠海马培养物轴突中,致密核心囊泡(DCV)和小清亮囊泡的聚集体是载体,它们在前往发育中突触的途中携带预先形成的AZ和突触囊泡(SV)成分。这些聚集体用抗巴松管蛋白和短笛蛋白(两种AZ细胞基质蛋白)、VAMP、SV2、突触结合蛋白(三种SV膜蛋白)以及突触蛋白I(一种与SV相关的蛋白)的抗体进行阳性标记。巴松管蛋白和短笛蛋白标记定位于聚集体和AZ中的致密物质处。除了突触处的SV外,SV膜蛋白还标记了聚集体中的清亮囊泡以及轴突中许多其他类似SV和多形性囊泡结构,并且突触蛋白I标记与聚集体中的囊泡相关。在单张切片中,这些轴突囊泡聚集体的平均尺寸约为0.22×0.13微米,包含一到两个DCV和五到六个小清亮囊泡。连续切片证实这些聚集体不是从正面切开的突触连接。从连续切片的运输聚集体和AZ测量的巴松管蛋白和短笛蛋白的标记强度在彼此范围内,这表明一个或几个聚集体,而不是单个DCV,可以携带足够的巴松管蛋白和短笛蛋白来形成一个AZ。本研究结果提供了首个超微结构证据,将各种AZ和SV蛋白定位在一个预先组装好的多囊泡运输聚集体中,该聚集体有潜力快速形成一个功能性活性区。