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使用亚细胞尺寸电极阵列对体外神经元进行局部电刺激。

Localized electrical stimulation of in vitro neurons using an array of sub-cellular sized electrodes.

机构信息

Bioelectronics Group, Imec, Kapeldreef 75, 3001 Heverlee, Belgium.

出版信息

Biosens Bioelectron. 2010 Dec 15;26(4):1474-7. doi: 10.1016/j.bios.2010.07.086. Epub 2010 Jul 30.

Abstract

The investigation of single-neuron parameters is of great interest because many aspects in the behavior and communication of neuronal networks still remain unidentified. However, the present available techniques for single-cell measurements are slow and do not allow for a high-throughput approach. We present here a CMOS compatible microelectrode array with 84 electrodes (with diameters ranging from 1.2 to 4.2 μm) that are smaller than the size of cell, thereby supporting single-cell addressability. We show controllable electroporation of a single cell by an underlying electrode while monitoring changes in the intracellular membrane potential. Further, by applying a localized electrical field between two electrodes close to a neuron while recording changes in the intracellular calcium concentration, we demonstrate activation of a single cell (∼270%, DF/F(0)), followed by a network response of the neighboring cells. The technology can be easily scaled up to larger electrode arrays (theoretically up to 137,000 electrodes/mm(2)) with active CMOS electronics integration able to perform high-throughput measurements on single cells.

摘要

单细胞参数的研究非常重要,因为神经元网络的许多行为和通讯方面仍然不明确。然而,目前用于单细胞测量的技术速度较慢,不允许采用高通量方法。我们在此提出了一种与 CMOS 兼容的微电极阵列,具有 84 个电极(直径范围从 1.2 到 4.2μm),小于细胞的大小,从而支持单细胞可寻址性。我们通过下面的电极显示出可以对单个细胞进行可控电穿孔,同时监测细胞内膜电位的变化。此外,通过在靠近神经元的两个电极之间施加局部电场,同时记录细胞内钙浓度的变化,我们证明了单个细胞的激活(约 270%,DF/F(0)),随后是相邻细胞的网络反应。该技术可以很容易地扩展到更大的电极阵列(理论上可以达到 137,000 个电极/mm(2)),并具有能够对单细胞进行高通量测量的有源 CMOS 电子集成。

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