Hu Wei-Wen, Chen Yen-Chi, Tsao Chia-Wen, Chen Shen-Liang, Tzeng Chung-Yuh
Department of Chemical and Materials Engineering National Central University Taoyuan Taiwan.
Department of Mechanical Engineering National Central University Taoyuan Taiwan.
Bioeng Transl Med. 2023 Dec 7;9(2):e10633. doi: 10.1002/btm2.10633. eCollection 2024 Mar.
A multifunctional bioreactor was fabricated in this study to investigate the facilitation efficiency of electrical and mechanical stimulations on myogenic differentiation. This bioreactor consisted of a highly stretchable conductive membrane prepared by depositing polypyrrole (PPy) on a flexible polydimethylsiloxane (PDMS) film. The tensile deformation of the PPy/PDMS membrane can be tuned by adjusting the channel depth. In addition, PPy/PDMS maintained its electrical conductivity under continuous cyclic stretching in the strain range of 6.5%-13% for 24 h. This device can be used to individually or simultaneously perform cyclic stretching and electrical stimulation. The results of single stimulation showed that either cyclic stretching or electrical stimulation upregulated myogenic gene expression and promoted myotube formation, where electrical stimulation improved better than cyclic stretching. However, only cyclic stretching can align C2C12 cells perpendicular to the stretching direction, and electrical stimulation did not affect cell morphology. Myosin heavy chain (MHC) immunostaining demonstrated that oriented cells under cyclic stretching resulted in parallel myotubes. The combination of these two stimuli exhibited synergetic effects on both myogenic gene regulation and myotube formation, and the incorporated electrical field did not affect the orientation effect of the cyclic stretching. These results suggested that these two treatments likely influenced cells through different pathways. Overall, the simultaneous application of cyclic stretching and electrical stimulation preserved both stimuli's advantages, so myo-differentiation can be highly improved to obtain abundant parallel myotubes, suggesting that our developed multifunctional bioreactor should benefit muscle tissue engineering applications.
本研究制备了一种多功能生物反应器,以研究电刺激和机械刺激对成肌分化的促进效率。该生物反应器由在柔性聚二甲基硅氧烷(PDMS)薄膜上沉积聚吡咯(PPy)制备的高拉伸性导电膜组成。PPy/PDMS膜的拉伸变形可通过调整通道深度来调节。此外,PPy/PDMS在6.5%-13%的应变范围内连续循环拉伸24小时后仍保持其导电性。该装置可用于单独或同时进行循环拉伸和电刺激。单一刺激的结果表明,循环拉伸或电刺激均可上调成肌基因表达并促进肌管形成,其中电刺激的效果优于循环拉伸。然而,只有循环拉伸能使C2C12细胞垂直于拉伸方向排列,而电刺激不影响细胞形态。肌球蛋白重链(MHC)免疫染色表明,循环拉伸下定向排列的细胞形成了平行的肌管。这两种刺激的组合在成肌基因调控和肌管形成方面均表现出协同效应,且外加电场不影响循环拉伸的定向作用。这些结果表明,这两种处理可能通过不同途径影响细胞。总体而言,循环拉伸和电刺激的同时应用保留了两种刺激的优点,因此可以显著提高肌分化以获得大量平行肌管,这表明我们开发的多功能生物反应器应有利于肌肉组织工程应用。