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Combining optogenetics and electrophysiology to analyze projection neuron circuits

机译:结合光遗传学和电生理学来分析投射神经元回路

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摘要

A set of methods is described for channelrhodopsin-2 (ChR2) based synaptic circuit analysis that combines photostimulation of virally transfected presynaptic neurons’ axons with whole-cell electrophysiological recordings from retrogradely labeled postsynaptic neurons. The approach exploits the preserved photoexcitability of ChR2-expressing axons in brain slices, and can be used to assess either local or long-range functional connections. Stereotaxic injections are used both to express ChR2 selectively in presynaptic axons of interest (using rabies or adeno-associated viruses) and to label two types of postsynaptic projection neurons of interest with fluorescent retrograde tracers. In brain slices, tracer-labeled postsynaptic neurons are targeted for whole-cell electrophysiological recordings, and synaptic connections are assessed by sampling voltage or current responses to LED photostimulation of ChR2-expressing axons. The data are analyzed to estimate the relative amplitude of synaptic input and other connectivity parameters. Pharmacological and electrophysiological manipulations extend the versatility of the basic approach, allowing dissection of monosynaptic versus disynaptic responses, excitatory versus inhibitory responses, and more. The method enables rapid, quantitative characterization of synaptic connectivity between defined pre- and postsynaptic classes of neurons.
机译:描述了一套基于通道视紫红质2(ChR2)的突触回路分析的方法,该方法将病毒转染的突触前神经元轴突的光刺激与逆行标记的突触后神经元的全细胞电生理记录结合起来。该方法利用了保留在大脑切片中表达ChR2的轴突的光激发性,可用于评估局部或远程功能连接。立体定向注射既可用于在感兴趣的突触前轴突中选择性表达ChR2(使用狂犬病或腺相关病毒),也可用于通过荧光逆行示踪剂标记两种类型的感兴趣的突触后投射神经元。在脑片中,示踪剂标记的突触后神经元被靶向进行全细胞电生理记录,并且通过采样对表达ChR2的轴突的LED光刺激的电压或电流响应来评估突触连接。分析数据以估计突触输入和其他连通性参数的相对幅度。药理学和电生理学操作扩展了基本方法的多功能性,可以解剖单突触反应与突触反应,兴奋反应与抑制反应等。该方法可以对突触前和突触后神经元类别之间的突触连接进行快速,定量的表征。

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