Department of Physiology and Biophysics and Rappaport Institute, Technion Faculty of Medicine, and Network Biology Research Laboratories, Lorry Lokey Center for Life Sciences and Engineering, Haifa 32000, Israel.
J Neurosci. 2011 Nov 16;31(46):16770-80. doi: 10.1523/JNEUROSCI.3384-11.2011.
Recent studies indicate that synaptic vesicles (SVs) are continuously interchanged among nearby synapses at very significant rates. These dynamics and the lack of obvious barriers confining synaptic vesicles to specific synapses would seem to challenge the ability of synapses to maintain a constant amount of synaptic vesicles over prolonged time scales. Moreover, the extensive mobilization of synaptic vesicles associated with presynaptic activity might be expected to intensify this challenge. Here we examined the ability of individual presynaptic boutons of rat hippocampal neurons to maintain their synaptic vesicle content, and the degree to which this ability is affected by continuous activity. We found that the synaptic vesicle content of individual boutons belonging to the same axons gradually changed over several hours, and that these changes occurred independently of activity. Intermittent stimulation for 1 h accelerated rates of vesicle pool size change. Interestingly, however, following stimulation cessation, vesicle pool size change rates gradually converged with basal change rates. Over similar time scales, active zones (AZs) exhibited substantial remodeling; yet, unlike synaptic vesicles, AZ remodeling was not affected by the stimulation paradigms used here. These findings indicate that enhanced activity levels can increase synaptic vesicle redistribution among nearby synapses, but also highlight the presence of forces that act to restore particular set points in terms of SV contents, and support a role for active zones in preserving such set points. These findings also indicate, however, that neither AZ size nor SV content set points are particularly stable, questioning the long-term tenacity of presynaptic specializations.
最近的研究表明,突触小泡(SVs)以非常高的速率在邻近的突触之间不断交换。这些动态变化以及缺乏明显的限制突触小泡局限于特定突触的障碍,似乎挑战了突触在长时间尺度上维持恒定突触小泡数量的能力。此外,与突触前活动相关的突触小泡的广泛动员可能会加剧这种挑战。在这里,我们检查了大鼠海马神经元的单个突触前末梢维持其突触小泡含量的能力,以及这种能力受到连续活动影响的程度。我们发现,属于同一轴突的单个末梢的突触小泡含量在数小时内逐渐发生变化,并且这些变化与活动无关。持续 1 小时的间歇性刺激加速了囊泡池大小变化的速率。然而,有趣的是,刺激停止后,囊泡池大小变化的速率逐渐与基础变化速率趋同。在相似的时间尺度上,活性区(AZs)经历了实质性的重塑;然而,与突触小泡不同,AZ 重塑不受这里使用的刺激方案的影响。这些发现表明,增强的活动水平可以增加邻近突触之间的突触小泡再分配,但也强调了存在作用于恢复特定 SV 含量设定点的力,并支持活性区在维持这些设定点方面的作用。然而,这些发现还表明,AZ 大小或 SV 含量设定点都不是特别稳定,这对突触前特化的长期稳定性提出了质疑。