Fernandez-Alfonso Tomas, Ryan Timothy A
Department of Biochemistry, Weill Medical College of Cornell University, 1300 York Ave, New York, NY 10021, USA.
Brain Cell Biol. 2008 Aug;36(1-4):87-100. doi: 10.1007/s11068-008-9030-y. Epub 2008 Oct 22.
Using pHluorin-tagged synaptic vesicle proteins we have examined the partitioning of these probes into recycling and nonrecycling pools at hippocampal nerve terminals in cell culture. Our studies show that for three of the major synaptic vesicle components, vGlut-1, VAMP-2, and Synaptotagmin I, approximately 50-60% of the tagged protein appears in a recycling pool that responds readily to sustained action potential stimulation by mobilizing and fusing with the plasma membrane, while the remainder is targeted to a nonrecycling, acidic compartment. The fraction of recycling and nonrecycling (or resting) pools varied significantly across boutons within an individual axon, from 100% resting (silent) to 100% recycling. Single-bouton bleaching studies show that recycling and resting pools are dynamic and exchange between synaptic boutons. The quantitative parameters that can be extracted with the approaches outlined here should help elucidate the potential functional role of the resting vesicle pool.
我们使用pHluorin标记的突触小泡蛋白,研究了这些探针在细胞培养的海马神经末梢中进入循环池和非循环池的分配情况。我们的研究表明,对于三种主要的突触小泡成分,即囊泡谷氨酸转运体1(vGlut-1)、囊泡相关膜蛋白2(VAMP-2)和突触结合蛋白I,大约50%-60%的标记蛋白出现在一个循环池中,该循环池通过与质膜动员和融合,对持续的动作电位刺激有快速反应,而其余部分则靶向一个非循环的酸性区室。在单个轴突内的不同突触扣结中,循环池和非循环(或静止)池的比例差异很大,从100%静止(沉默)到100%循环。单突触扣结漂白研究表明,循环池和静止池是动态的,并且在突触扣结之间相互交换。通过本文所述方法可以提取的定量参数,应有助于阐明静止囊泡池的潜在功能作用。