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基于电荷注入的聚吡咯平面电极电刺激调节细胞成骨分化

Charge injection based electrical stimulation on polypyrrole planar electrodes to regulate cellular osteogenic differentiation.

作者信息

Liu Zongguang, Dong Lingqing, Cheng Kui, Luo Zhongkuan, Weng Wenjian

机构信息

School of Materials Science and Engineering, State Key Laboratory of Silicon Materials, Zhejiang University Hangzhou 310027 China

The Affiliated Stomatologic Hospital, School of Medicine, Zhejiang University Hangzhou 310003 China.

出版信息

RSC Adv. 2018 May 21;8(33):18470-18479. doi: 10.1039/c8ra02601g. eCollection 2018 May 17.

Abstract

In this study, polypyrrole (Ppy) electrodes were prepared to support an electrical stimulation to MC3T3-E1 cells for regulating their osteogenic differentiation. The charge injection capacity ( ) of the Ppy electrodes could be adjusted by the Ppy thickness, and a higher could make the electrode able to produce a higher charge injection quantity ( ) at applied voltage. The onto electrode could be considered as the intensity of the stimulation pulse to cells, and the pulse frequency means the number of electric stimulation with at one second. Hence, we conducted the present work in the view of . When the cells were electrically stimulated for 1 hour per day, the electrodes with ranged in 0.08-0.15 μQ had an obvious role in enhancing cellular osteogenic differentiation whereas of lower than 0.03 μQ or more than 0.30 μQ gave the stimulations with no or negative effects. And the stimulation with 1 or 25 Hz showed to enhance the differentiation, whereas the stimulation with 50 Hz gave an inhibiting effect. We further found the osteogenic differentiation potential triggered by electrical simulation was related to cell growth stage, and the stimulation carried out at early stage (day 2-5) during 8 days cell culture showed more contribution to enhancing osteogenic differentiation than that at later stage (day 6-8). It is proposed that the desired stimulation effects require that an appropriate voltage-gated calcium ion channel and efficient intracellular calcium ion oscillation are well activated. This work therefore reveals as an important electrode parameter to decide effective simulations and provides an insight into understanding of the role of electrode material characters in regulating cellular osteogenic differentiation during stimulation.

摘要

在本研究中,制备了聚吡咯(Ppy)电极以支持对MC3T3-E1细胞的电刺激,从而调节其成骨分化。Ppy电极的电荷注入容量( )可通过Ppy厚度进行调节,较高的 可使电极在施加电压时能够产生更高的电荷注入量( )。电极上的 可被视为对细胞刺激脉冲的强度,而脉冲频率表示每秒具有 的电刺激次数。因此,我们从 的角度开展了本工作。当细胞每天接受1小时电刺激时, 在0.08 - 0.15 μQ范围内的电极对增强细胞成骨分化具有明显作用,而低于0.03 μQ或高于0.30 μQ的 给予的刺激无作用或具有负面影响。1 Hz或25 Hz的刺激显示可增强分化,而50 Hz的刺激则具有抑制作用。我们进一步发现,电模拟引发的成骨分化潜能与细胞生长阶段有关,在8天细胞培养的早期阶段(第2 - 5天)进行的刺激比后期阶段(第6 - 8天)对增强成骨分化的贡献更大。有人提出,期望的刺激效果需要适当激活电压门控钙离子通道并有效进行细胞内钙离子振荡。因此,这项工作揭示了 作为决定有效模拟的重要电极参数,并为理解电极材料特性在刺激过程中调节细胞成骨分化的作用提供了见解。

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