Ion Chat Research Corporation, Saitama, Japan.
J Neurophysiol. 2019 Nov 1;122(5):2016-2026. doi: 10.1152/jn.00359.2019. Epub 2019 Sep 4.
Observations of the electrophysiological properties of cells are important for understanding cellular functions and their underlying mechanisms. Short action potentials in axons are essential to rapidly deliver signals from the neuronal cell body to the terminals, whereas longer action potentials are required for sufficient calcium influx for transmitter release at the synaptic terminals and for cardiomyocyte and smooth muscle contractions. To accurately observe the shape and timing of depolarizations, it is essential to measure changes in the intracellular membrane potential. The ability to record action potentials and intracellular membrane potentials from mammalian cells and neurons was made possible by Ling and Gerard's discovery in 1949, when they introduced sharp glass electrode with a submicron sized tip. Because of the small tip size, the sharp glass electrode could penetrate the cell membrane with little damage, which was one of the major breakthroughs in cellular electrophysiology and is the basic principle of the intracellular recording technique to date, providing the basis for further innovation of patch-clamp electrophysiology. I report a proof-of-principle demonstration of a novel method for recording intracellular potentials without penetrating the cell membrane using glass electrodes. We discovered that magnetically held transmembrane conductive nanoparticles can function as an intracellular electrode to detect transmembrane membrane potentials similar to those obtained by the conventional patch-clamp recording method. To accurately observe the shape of action potentials, it is essential to perform intracellular recordings. I present a method to record intracellular potentials using magnetically held magnetic conductive nanoparticles in the membrane as an electrode. These nanoparticles function similarly to a conventional intracellular microelectrode. This is the first report to apply conductive nanoparticles to detect action potentials in the form of electrical signals.
观察细胞的电生理特性对于理解细胞功能及其潜在机制非常重要。轴突中的短动作电位对于快速将信号从神经元细胞体传递到末端至关重要,而较长的动作电位则需要足够的钙离子内流以在突触末端释放递质,并使心肌细胞和平滑肌收缩。为了准确观察去极化的形状和时间,测量细胞内膜电位的变化至关重要。1949 年,Ling 和 Gerard 发现了一种带有亚微米尺寸尖端的锋利玻璃电极,使测量哺乳动物细胞和神经元的动作电位和细胞内膜电位的能力成为可能。由于尖端尺寸小,锋利的玻璃电极可以在对细胞膜造成最小损伤的情况下穿透细胞膜,这是细胞电生理学的重大突破之一,也是迄今为止细胞内记录技术的基本原理,为膜片钳电生理学的进一步创新提供了基础。我报告了一种使用玻璃电极记录细胞内电势而无需穿透细胞膜的新方法的原理验证演示。我们发现,通过磁场保持的跨膜导电纳米颗粒可以作为一种检测跨膜膜电位的细胞内电极,其功能类似于传统的膜片钳记录方法。为了准确观察动作电位的形状,进行细胞内记录是必不可少的。我提出了一种使用磁保持的膜内磁性导电纳米颗粒作为电极记录细胞内电势的方法。这些纳米颗粒的功能类似于传统的细胞内微电极。这是首次应用导电纳米颗粒以电信号形式检测动作电位的报告。