SUPA Department of Biomedical Engineering, University of Strathclyde, Glasgow, G1 1QE, UK.
Centre for the Cellular Microenvironment, Division of Biomedical Engineering, School of Engineering, College of Science and Engineering, University of Glasgow, Glasgow, G12 8QQ, UK.
Sci Rep. 2019 Sep 10;9(1):12944. doi: 10.1038/s41598-019-49422-4.
In regenerative medicine, techniques which control stem cell lineage commitment are a rapidly expanding field of interest. Recently, nanoscale mechanical stimulation of mesenchymal stem cells (MSCs) has been shown to activate mechanotransduction pathways stimulating osteogenesis in 2D and 3D culture. This has the potential to revolutionise bone graft procedures by creating cellular graft material from autologous or allogeneic sources of MSCs without using chemical induction. With the increased interest in mechanical stimulation of cells and huge potential for clinical use, it is apparent that researchers and clinicians require a scalable bioreactor system that provides consistently reproducible results with a simple turnkey approach. A novel bioreactor system is presented that consists of: a bioreactor vibration plate, calibrated and optimised for nanometre vibrations at 1 kHz, a power supply unit, which supplies a 1 kHz sine wave signal necessary to generate approximately 30 nm of vibration amplitude, and custom 6-well cultureware with toroidal shaped magnets incorporated in the base of each well for conformal attachment to the bioreactor's magnetic vibration plate. The cultureware and vibration plate were designed using finite element analysis to determine the modal and harmonic responses, and validated by interferometric measurement. This helps ensure that the vibration plate and cultureware, and thus collagen and MSCs, all move as a rigid body, avoiding large deformations close to the resonant frequency of the vibration plate and vibration damping beyond the resonance. Assessment of osteogenic protein expression was performed to confirm differentiation of MSCs after initial biological experiments with the system, as well as atomic force microscopy of the 3D gel constructs during vibrational stimulation to verify that strain hardening of the gel did not occur. This shows that cell differentiation was the result of the nanovibrational stimulation provided by the bioreactor alone, and that other cell differentiating factors, such as stiffening of the collagen gel, did not contribute.
在再生医学中,控制干细胞谱系定向的技术是一个快速发展的研究领域。最近,已经证明对间充质干细胞(MSCs)的纳米级机械刺激可激活机械转导途径,从而刺激 2D 和 3D 培养中的成骨作用。这有可能通过使用源自自体或同种异体来源的 MSCs 的细胞移植物材料来彻底改变骨移植物程序,而无需使用化学诱导。由于对细胞机械刺激的兴趣增加以及巨大的临床应用潜力,研究人员和临床医生显然需要一种可扩展的生物反应器系统,该系统可以通过简单的交钥匙方法提供一致且可重复的结果。提出了一种新型的生物反应器系统,该系统包括:生物反应器振动板,经过校准和优化,可在 1 kHz 时产生纳米级振动;电源单元,可提供 1 kHz 正弦波信号,该信号对于产生约 30nm 的振动幅度是必需的;定制的 6 孔培养板,其底部装有环形磁铁,可与生物反应器的磁性振动板贴合。使用有限元分析设计了培养板和振动板,以确定模态和谐波响应,并通过干涉测量进行了验证。这有助于确保振动板和培养板以及胶原和 MSCs 都作为一个刚体移动,从而避免在接近振动板的共振频率时发生大变形和超过共振时的振动衰减。进行成骨蛋白表达评估,以确认初始生物实验后 MSCs 的分化,以及在振动刺激期间对 3D 凝胶结构进行原子力显微镜检查,以验证凝胶不会发生应变硬化。这表明细胞分化是生物反应器单独提供的纳米振动刺激的结果,而其他细胞分化因素(例如胶原凝胶的变硬)并未起作用。