⊥Department of Neurosurgery, Spine, and Spinal Cord Institute, College of Medicine, Yonsei University, Seoul 120-752, Republic of Korea.
¶Department of Physics, Chonbuk National University, Jeonju 561-756, Republic of Korea.
Nano Lett. 2015 Aug 12;15(8):5414-9. doi: 10.1021/acs.nanolett.5b01810. Epub 2015 Jul 17.
Electrical stimulation through direct electrical activation has been widely used to recover the function of neurons, primarily through the extracellular application of thin film electrodes. However, studies using extracellular methods show limited ability to reveal correlations between the cells and the electrical stimulation due to interference from external sources such as membrane capacitance and culture medium. Here, we demonstrate long-term intracellular electrical stimulation of undamaged pheochromocytoma (PC-12) cells by utilizing a vertical nanowire electrode array (VNEA). The VNEA was prepared by synthesizing silicon nanowires on a Si substrate through a vapor-liquid-solid (VLS) mechanism and then fabricating them into electrodes with semiconductor nanodevice processing. PC-12 cells were cultured on the VNEA for 4 days with intracellular electrical stimulation and then a 2-day stabilization period. Periodic scanning via two-photon microscopy confirmed that the electrodes pierced the cells without inducing damage. Electrical stimulation through the VNEA enhances cellular differentiation and neurite outgrowth by about 50% relative to extracellular stimulation under the same conditions. VNEA-mediated stimulation also revealed that cellular differentiation and growth in the cultures were dependent on the potential used to stimulate them. Intracellular stimulation using nanowires could pave the way for controlled cellular differentiation and outgrowth studies in living cells.
通过直接电激活进行电刺激已被广泛用于恢复神经元的功能,主要是通过在细胞外应用薄膜电极进行。然而,使用细胞外方法的研究由于膜电容和培养基等外部源的干扰,显示出对细胞和电刺激之间相关性的揭示能力有限。在这里,我们通过利用垂直纳米线电极阵列(VNEA)来展示对未受损的嗜铬细胞瘤(PC-12)细胞的长期细胞内电刺激。VNEA 通过在 Si 衬底上通过汽-液-固(VLS)机制合成硅纳米线,并通过半导体纳米器件处理将它们制成电极来制备。将 PC-12 细胞在 VNEA 上培养 4 天,进行细胞内电刺激,然后进行 2 天的稳定期。通过双光子显微镜进行定期扫描证实,电极刺穿细胞而不会引起损伤。与相同条件下的细胞外刺激相比,通过 VNEA 进行的电刺激可将细胞分化和突起生长提高约 50%。VNEA 介导的刺激还表明,培养物中的细胞分化和生长取决于用于刺激它们的电位。使用纳米线进行细胞内刺激可以为在活细胞中进行受控的细胞分化和突起生长研究铺平道路。