Laboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, University of Tokyo, Hongo, Tokyo, Japan.
J Physiol. 2012 Oct 1;590(19):4869-80. doi: 10.1113/jphysiol.2012.237685. Epub 2012 Jun 25.
The variation of individual synaptic transmission impacts the dynamics of complex neural circuits. We performed whole-cell recordings from monosynaptically connected hippocampal neurons in rat organotypic slice cultures using a synapse mapping method. The amplitude of unitary excitatory postsynaptic current (uEPSC) varied from trial to trial and was independent of the physical distance between cell pairs. To investigate the source of the transmission variability, we obtained patch-clamp recordings from intact axons. Axonal action potentials (APs) were reliably transmitted throughout the axonal arbour and showed modest changes in width. In contrast, calcium imaging from presynaptic boutons revealed that the amplitude of AP-evoked calcium transients exhibited large variations both among different boutons at a given trial and among trials in a given bouton. These results suggest that a factor contributing to the uEPSC fluctuations is the variability in calcium dynamics at presynaptic terminals. Finally, we acquired triple whole-cell recordings from divergent circuit motifs with one presynaptic neuron projecting to two postsynaptic neurons. Consistent with the independency of calcium dynamics among axonal boutons, a series of uEPSC fluctuations was not correlated between the two postsynaptic cells, indicating that different synapses even from the same neuron act independently.We conclude that the intra-bouton and inter-bouton variability in AP-induced calcium dynamics determine the heterogeneity and independency of uEPSCs.
个体突触传递的变化会影响复杂神经回路的动力学。我们使用突触映射方法在大鼠器官型切片培养物中单突触连接的海马神经元上进行全细胞记录。单位兴奋性突触后电流 (uEPSC) 的幅度在试验之间变化,与细胞对之间的物理距离无关。为了研究传输变异性的来源,我们从完整的轴突获得了膜片钳记录。轴突动作电位 (AP) 在整个轴突树突中可靠传递,并且宽度略有变化。相比之下,从突触前末梢进行钙成像显示,在给定的试验中,AP 诱发的钙瞬变幅度在不同末梢之间以及在同一末梢的不同试验之间都有很大的变化。这些结果表明,导致 uEPSC 波动的一个因素是突触前末端钙动力学的可变性。最后,我们从具有一个突触前神经元投射到两个突触后神经元的发散回路模式中获得了三重全细胞记录。与轴突末梢之间钙动力学的独立性一致,两个突触后细胞之间的一系列 uEPSC 波动没有相关性,表明即使来自同一神经元的不同突触也独立发挥作用。我们得出结论,AP 诱导的钙动力学在末梢内和末梢间的变异性决定了 uEPSC 的异质性和独立性。