Intracellular recording of action potentials by nanopillar electroporation

纳米柱 细胞内 细胞外 材料科学 电极 生物物理学 离子通道 电穿孔 信号(编程语言) 纳米技术 化学 计算机科学 生物 生物化学 受体 物理化学 基因 纳米结构 程序设计语言
作者
Chong Xie,Ziliang Lin,Lindsey Hanson,Yi Cui,Bianxiao Cui
出处
期刊:Nature Nanotechnology [Nature Portfolio]
卷期号:7 (3): 185-190 被引量:571
标识
DOI:10.1038/nnano.2012.8
摘要

Action potentials have a central role in the nervous system and in many cellular processes, notably those involving ion channels. The accurate measurement of action potentials requires efficient coupling between the cell membrane and the measuring electrodes. Intracellular recording methods such as patch clamping involve measuring the voltage or current across the cell membrane by accessing the cell interior with an electrode, allowing both the amplitude and shape of the action potentials to be recorded faithfully with high signal-to-noise ratios1. However, the invasive nature of intracellular methods usually limits the recording time to a few hours1, and their complexity makes it difficult to simultaneously record more than a few cells. Extracellular recording methods, such as multielectrode arrays2 and multitransistor arrays3, are non-invasive and allow long-term and multiplexed measurements. However, extracellular recording sacrifices the one-to-one correspondence between the cells and electrodes, and also suffers from significantly reduced signal strength and quality. Extracellular techniques are not, therefore, able to record action potentials with the accuracy needed to explore the properties of ion channels. As a result, the pharmacological screening of ion-channel drugs is usually performed by low-throughput intracellular recording methods4. The use of nanowire transistors5,6,7, nanotube-coupled transistors8 and micro gold-spine and related electrodes9,10,11,12 can significantly improve the signal strength of recorded action potentials. Here, we show that vertical nanopillar electrodes can record both the extracellular and intracellular action potentials of cultured cardiomyocytes over a long period of time with excellent signal strength and quality. Moreover, it is possible to repeatedly switch between extracellular and intracellular recording by nanoscale electroporation and resealing processes. Furthermore, vertical nanopillar electrodes can detect subtle changes in action potentials induced by drugs that target ion channels. Arrays of vertical nanopillar electrodes can be used for both intracellular and extracellular recording with excellent signal strength and quality, and minimal damage to the cells.
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