Qi Guanxiao, Radnikow Gabriele, Feldmeyer Dirk
Institute of Neuroscience and Medicine (INM-2), Research Centre Jülich.
Institute of Neuroscience and Medicine (INM-2), Research Centre Jülich; Department of Psychiatry, Psychotherapy and Psychosomatics, Medical Faculty, JARA, RWTH Aachen University;
J Vis Exp. 2015 Jan 10(95):52358. doi: 10.3791/52358.
The combination of patch clamp recordings from two (or more) synaptically coupled neurons (paired recordings) in acute brain slice preparations with simultaneous intracellular biocytin filling allows a correlated analysis of their structural and functional properties. With this method it is possible to identify and characterize both pre- and postsynaptic neurons by their morphology and electrophysiological response pattern. Paired recordings allow studying the connectivity patterns between these neurons as well as the properties of both chemical and electrical synaptic transmission. Here, we give a step-by-step description of the procedures required to obtain reliable paired recordings together with an optimal recovery of the neuron morphology. We will describe how pairs of neurons connected via chemical synapses or gap junctions are identified in brain slice preparations. We will outline how neurons are reconstructed to obtain their 3D morphology of the dendritic and axonal domain and how synaptic contacts are identified and localized. We will also discuss the caveats and limitations of the paired recording technique, in particular those associated with dendritic and axonal truncations during the preparation of brain slices because these strongly affect connectivity estimates. However, because of the versatility of the paired recording approach it will remain a valuable tool in characterizing different aspects of synaptic transmission at identified neuronal microcircuits in the brain.
在急性脑片制备中,将来自两个(或更多)突触耦合神经元的膜片钳记录(配对记录)与细胞内生物素同时填充相结合,可以对它们的结构和功能特性进行相关分析。通过这种方法,可以根据形态学和电生理反应模式来识别和表征突触前和突触后神经元。配对记录有助于研究这些神经元之间的连接模式以及化学和电突触传递的特性。在这里,我们将逐步描述获得可靠配对记录以及神经元形态最佳恢复所需的程序。我们将描述如何在脑片制备中识别通过化学突触或缝隙连接相连的神经元对。我们将概述如何重建神经元以获得其树突和轴突区域的三维形态,以及如何识别和定位突触接触。我们还将讨论配对记录技术的注意事项和局限性,特别是与脑片制备过程中树突和轴突截断相关的问题,因为这些会严重影响连接性估计。然而,由于配对记录方法的多功能性,它仍将是表征大脑中已识别神经元微电路突触传递不同方面的宝贵工具。