Laboratory of Sensory Processing, Faculty of Life Sciences, Brain Mind Institute, École Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland.
Neuron. 2017 Sep 13;95(6):1266-1281. doi: 10.1016/j.neuron.2017.06.049.
Neuronal membrane potential is of fundamental importance for the mechanistic understanding of brain function. This review discusses progress in whole-cell patch-clamp recordings for low-noise measurement of neuronal membrane potential in awake behaving animals. Whole-cell recordings can be combined with two-photon microscopy to target fluorescently labeled neurons, revealing cell-type-specific membrane potential dynamics of retrogradely or genetically labeled neurons. Dual whole-cell recordings reveal behavioral modulation of membrane potential synchrony and properties of synaptic transmission in vivo. Optogenetic manipulations are also readily integrated with whole-cell recordings, providing detailed information about the effect of specific perturbations on the membrane potential of diverse types of neurons. Exciting developments for future behavioral experiments include dendritic whole-cell recordings and imaging, and use of the whole-cell recording pipette for single-cell delivery of drugs and DNA, as well as RNA expression profiling. Whole-cell recordings therefore offer unique opportunities for investigating the neuronal circuits and synaptic mechanisms driving membrane potential dynamics during behavior.
神经元膜电位对于理解大脑功能的机制至关重要。本综述讨论了在清醒活动动物中进行全细胞膜片钳记录以进行低噪声神经元膜电位测量的进展。全细胞膜片钳记录可与双光子显微镜结合,以靶向荧光标记的神经元,揭示逆行或基因标记神经元的细胞类型特异性膜电位动力学。双全细胞膜片钳记录揭示了膜电位同步和体内突触传递特性的行为调节。光遗传学操作也很容易与全细胞膜片钳记录相结合,提供有关特定干扰对不同类型神经元膜电位影响的详细信息。未来行为实验的令人兴奋的发展包括树突全细胞膜片钳记录和成像,以及使用全细胞膜片钳记录管进行单细胞给药和 DNA 以及 RNA 表达谱分析。因此,全细胞膜片钳记录为研究行为过程中驱动膜电位动力学的神经元回路和突触机制提供了独特的机会。
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