Simultaneous monitoring of action potentials and neurotransmitter release from neuron-like PC12 cells

被引:10
|
作者
Cui, Mei Rong [1 ,2 ]
Zhao, Wei [1 ,2 ]
Li, Xiang Ling [1 ,2 ]
Xu, Cong Hui [1 ,2 ]
Xu, Jing Juan [1 ,2 ]
Chen, Hong Yuan [1 ,2 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210023, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, Collaborat Innovat Ctr Chem Life Sci, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
Action potentials; Neurotransmitter; MEA/TIRFM; REFLECTION FLUORESCENCE MICROSCOPY; MICROELECTRODE ARRAYS; DOPAMINE RELEASE; CHROMAFFIN CELLS; HYPOXIA; EVENTS; DEPOLARIZATION; VESICLES; SURFACES; CHANNELS;
D O I
10.1016/j.aca.2019.11.074
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:74 / 81
页数:8
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