Institute of Molecular Medicine, Peking University, Beijing 100871, China.
J Physiol. 2011 May 1;589(Pt 9):2213-27. doi: 10.1113/jphysiol.2010.200154. Epub 2011 Feb 28.
Patterns of action potentials (APs), often in the form of bursts, are critical for coding and processing information in the brain. However, how AP bursts modulate secretion at synapses remains elusive. Here, using the calyx of Held synapse as a model we compared synaptic release evoked by AP patterns with a different number of bursts while the total number of APs and frequency were fixed. The ratio of total release produced by multiple bursts to that by a single burst was defined as 'burst-effect'.We found that four bursts of 25 stimuli at 100 Hz increased the totalcharge of EPSCs to 1.47 ± 0.04 times that by a single burst of 100 stimuli at the same frequency.Blocking AMPA receptor desensitization and saturation did not alter the burst-effect, indicating that it was mainly determined by presynaptic mechanisms. Simultaneous dual recordings of presynaptic membrane capacitance (Cm) and EPSCs revealed a similar burst-effect, being 1.58±0.13by Cm and 1.49±0.05 by EPSCs. Reducing presynapticCa2+ influx by lowering extracellular Ca2+concentration or buffering residual intracellular Ca2+ with EGTA inhibited the burst-effect. We further developed a computational model largely recapitulating the burst-effect and demonstrated that this effect is highly sensitive to dynamic change in availability of the releasable pool of synaptic vesicles during various patterns of activities. Taken together, we conclude that AP bursts modulate synaptic output mainly through intricate interaction between depletion and replenishment of the large releasable pool. This burst-effect differs from the somatic burst-effect previously described from adrenal chromaffin cells, which substantially depends on activity-induced accumulation of Ca2+ to facilitate release of a limited number of vesicles in the releasable pool. Hence, AP bursts may play an important role in dynamically regulating synaptic strength and fidelity during intense neuronal activity at central synapses.
动作电位 (AP) 的模式,通常以爆发的形式,对于大脑中的编码和信息处理至关重要。然而,AP 爆发如何调节突触处的分泌仍不清楚。在这里,我们使用 Held 球顶突触作为模型,比较了在固定 AP 总数和频率的情况下,具有不同爆发数的 AP 模式诱发的突触释放。多个爆发产生的总释放与单个爆发产生的总释放的比值定义为“爆发效应”。我们发现,在 100 Hz 时,25 个刺激的四个爆发将 EPSC 的总电荷量增加到单个爆发的 1.47±0.04 倍,该爆发由相同频率的 100 个刺激产生。阻断 AMPA 受体脱敏和饱和不会改变爆发效应,表明它主要由突触前机制决定。同时记录突触前膜电容 (Cm) 和 EPSC 的双记录揭示了相似的爆发效应,Cm 为 1.58±0.13,EPSC 为 1.49±0.05。通过降低细胞外 Ca2+浓度或用 EGTA 缓冲残留的细胞内 Ca2+来减少突触前 Ca2+内流抑制了爆发效应。我们进一步开发了一个计算模型,很大程度上再现了爆发效应,并证明这种效应对各种活动模式下可释放囊泡池的可用性的动态变化非常敏感。总之,我们得出结论,AP 爆发主要通过大的可释放囊泡池的耗竭和再填充之间的复杂相互作用来调节突触输出。这种爆发效应不同于先前从肾上腺嗜铬细胞描述的躯体爆发效应,它主要依赖于活动诱导的 Ca2+积累,以促进可释放池中的有限数量囊泡的释放。因此,AP 爆发可能在中枢突触的强烈神经元活动期间动态调节突触强度和保真度方面发挥重要作用。