Development of a three-dimensional direct current electric field stimulation bioreactor to enhance the axonal outgrowth and control the axonal orientation

Q4 Engineering
E. Nakamachi, Shohei Tanaka, Koji Yamamoto, Y. Morita, Manabu Okita
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引用次数: 2

Abstract

Until now, numerous studies on the effects of electrical stimulation on nerve cell activation in a cell culture have been conducted. However, there are very few studies that have used the three-dimensional (3D) culture system to investigate nerve cell axonal extension. In this study, we developed a novel 3D direct current electric field (DCEF) stimulation bioreactor, which can uniformly stimulate cultured nerve cells for a long period. We observed the morphogenesis of PC12 cells using a multi photon excitation fluorescence microscope (MPM) and evaluated DCEF stimulation effects on PC12 cells axonal outgrowth. First, a DCEF stimulation bioreactor was designed using finite element analysis for uniform electric field. We, then, validated the uniform stimulation of PC12 cells using this bioreactor for 24 h. Second, we determined the optimal stimulation condition using the response surface method and adopting objective functions, such as axonal length, the ratio of axonal orientation towards the anode, and design parameters, such as the electric field strength and the duration of the stimulation. We found the optimal condition to be 43 mV/mm and 6.2 h/day for axonal length enhancement. An increase of 20.1% against the condition for the control group (Mann-Whitney’s U test, p<0.05) was obtained. In addition, the 92 % of PC12 cells were oriented toward the anode with 90 mV/mm, 24 h/day condition. However, the axonal formation was suppressed depending on the stimulation duration. Finally, we found the optimal conditions of 70 mV/mm and 7.9 h/day for achieving the enhancement of axonal extension and orientation, simultaneously.
三维直流电场刺激生物反应器的研制,以促进轴突生长和控制轴突方向
到目前为止,已经进行了大量关于电刺激对细胞培养中神经细胞激活的影响的研究。然而,利用三维(3D)培养系统研究神经细胞轴突延伸的研究很少。在本研究中,我们开发了一种新型的三维直流电场(DCEF)刺激生物反应器,它可以长时间均匀地刺激培养的神经细胞。利用多光子激发荧光显微镜(MPM)观察PC12细胞的形态发生,并评价DCEF刺激对PC12细胞轴突生长的影响。首先,采用均匀电场有限元法设计了DCEF刺激生物反应器。然后,我们利用该生物反应器对PC12细胞进行了24 h的均匀刺激验证。其次,我们采用响应面法和目标函数(如轴突长度、轴突朝向阳极的比例)以及设计参数(如电场强度和刺激持续时间)确定了最佳刺激条件。结果表明,在43 mV/mm、6.2 h/d的强度下,轴突长度增强效果最佳。与对照组相比,增加了20.1% (Mann-Whitney 's U检验,p<0.05)。此外,92%的PC12电池在90 mV/mm、24 h/day的条件下向阳极定向。然而,轴突的形成受到不同刺激时间的抑制。最后,我们找到了70 mV/mm和7.9 h/d同时实现轴突伸展和定向增强的最佳条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Biomechanical Science and Engineering
Journal of Biomechanical Science and Engineering Engineering-Biomedical Engineering
CiteScore
0.90
自引率
0.00%
发文量
18
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