Rubinski Anna, Ziv Noam E
Rappaport Faculty of Medicine, Network Biology Research Laboratories, Technion, Haifa, Israel.
PLoS Comput Biol. 2015 Nov 24;11(11):e1004632. doi: 10.1371/journal.pcbi.1004632. eCollection 2015 Nov.
Glutamatergic synapse size remodeling is governed not only by specific activity forms but also by apparently stochastic processes with well-defined statistics. These spontaneous remodeling processes can give rise to skewed and stable synaptic size distributions, underlie scaling of these distributions and drive changes in glutamatergic synapse size "configurations". Where inhibitory synapses are concerned, however, little is known on spontaneous remodeling dynamics, their statistics, their activity dependence or their long-term consequences. Here we followed individual inhibitory synapses for days, and analyzed their size remodeling dynamics within the statistical framework previously developed for glutamatergic synapses. Similar to glutamatergic synapses, size distributions of inhibitory synapses were skewed and stable; at the same time, however, sizes of individual synapses changed considerably, leading to gradual changes in synaptic size configurations. The suppression of network activity only transiently affected spontaneous remodeling dynamics, did not affect synaptic size configuration change rates and was not followed by the scaling of inhibitory synapse size distributions. Comparisons with glutamatergic synapses within the same dendrites revealed a degree of coupling between nearby inhibitory and excitatory synapse remodeling, but also revealed that inhibitory synapse size configurations changed at considerably slower rates than those of their glutamatergic neighbors. These findings point to quantitative differences in spontaneous remodeling dynamics of inhibitory and excitatory synapses but also reveal deep qualitative similarities in the processes that control their sizes and govern their remodeling dynamics.
谷氨酸能突触大小重塑不仅受特定活动形式的调控,还受具有明确统计规律的明显随机过程的影响。这些自发重塑过程可导致突触大小分布的偏态和稳定,是这些分布缩放的基础,并驱动谷氨酸能突触大小“构型”的变化。然而,对于抑制性突触,人们对其自发重塑动力学、统计规律、活动依赖性或长期后果知之甚少。在此,我们对单个抑制性突触进行了数天的跟踪,并在先前为谷氨酸能突触建立的统计框架内分析了它们的大小重塑动力学。与谷氨酸能突触类似,抑制性突触的大小分布也是偏态且稳定的;然而,与此同时,单个突触的大小发生了相当大的变化,导致突触大小构型逐渐改变。网络活动的抑制仅短暂影响自发重塑动力学,不影响突触大小构型变化率,且抑制性突触大小分布不会随之缩放。对同一树突内谷氨酸能突触的比较显示,附近抑制性和兴奋性突触重塑之间存在一定程度的耦合,但也表明抑制性突触大小构型的变化速率比其谷氨酸能邻居慢得多。这些发现指出了抑制性和兴奋性突触自发重塑动力学的定量差异,但也揭示了在控制其大小和支配其重塑动力学的过程中存在深刻的定性相似性。