State Key Laboratory of Analytical Chemistry for Life Science and Collaborative Innovation Center of Chemistry for Life Sciences, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, PR China.
State Key Laboratory of Analytical Chemistry for Life Science and Collaborative Innovation Center of Chemistry for Life Sciences, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, PR China.
Anal Chim Acta. 2020 Apr 8;1105:74-81. doi: 10.1016/j.aca.2019.11.074. Epub 2020 Jan 20.
Simultaneous recording of action potentials (APs) and neurotransmitter release is highly desirable in living neurons since it provides a complete framework of the physiological and pathological statuses of nerve cells. In this work, we proposed an approach coupling ultra-thin microelectrode array (MEA) with total internal reflection fluorescence microscopy (TIRFM), which served as a powerful platform to visualize both APs and vesicular exocytosis in a neuronal circuit model formed by neuron-like PC12 cells. Taking advantages of fluorescent false neurotransmitter (FFN), the transient neurotransmitter transport down an axon could be visualized with high spatial and temporal resolution. The real-time recording of APs burst and neurotransmitter release induced by hypoxia with MEA/TIRFM platform reveals the relevance of electrical and chemical activities in the neuronal model. The combination of the optical and electrical techniques enables mapping of neuron connectivity in an entire neuronal circuit, which may ultimately lead to deeper understanding of nervous system.
在活体神经元中,同时记录动作电位 (APs) 和神经递质释放是非常理想的,因为它为神经元的生理和病理状态提供了一个完整的框架。在这项工作中,我们提出了一种将超微电极阵列 (MEA) 与全内反射荧光显微镜 (TIRFM) 结合的方法,该方法作为一个强大的平台,可以可视化神经元样 PC12 细胞形成的神经元回路模型中的 APs 和囊泡胞吐作用。利用荧光假神经递质 (FFN),可以高时空分辨率可视化轴突中瞬时神经递质的转运。MEA/TIRFM 平台实时记录缺氧诱导的 APs 爆发和神经递质释放,揭示了神经元模型中电和化学活动的相关性。光学和电学技术的结合使得能够在整个神经元回路中绘制神经元连接图,这可能最终导致对神经系统的更深入理解。