Bahmaee Hossein, Owen Robert, Boyle Liam, Perrault Cecile M, Garcia-Granada Andres A, Reilly Gwendolen C, Claeyssens Frederik
Department of Materials Science and Engineering, Kroto Research Institute, The University of Sheffield, Sheffield, United Kingdom.
INSIGNEO Institute for in silico Medicine, The University of Sheffield, Sheffield, United Kingdom.
Front Bioeng Biotechnol. 2020 Sep 8;8:557111. doi: 10.3389/fbioe.2020.557111. eCollection 2020.
Microfluidic-based tissue-on-a-chip devices have generated significant research interest for biomedical applications, such as pharmaceutical development, as they can be used for small volume, high throughput studies on the effects of therapeutics on tissue-mimics. Tissue-on-a-chip devices are evolving from basic 2D cell cultures incorporated into microfluidic devices to complex 3D approaches, with modern designs aimed at recapitulating the dynamic and mechanical environment of the native tissue. Thus far, most tissue-on-a-chip research has concentrated on organs involved with drug uptake, metabolism and removal (e.g., lung, skin, liver, and kidney); however, models of the drug metabolite target organs will be essential to provide information on therapeutic efficacy. Here, we develop an osteogenesis-on-a-chip device that comprises a 3D environment and fluid shear stresses, both important features of bone. This inexpensive, easy-to-fabricate system based on a polymerized High Internal Phase Emulsion (polyHIPE) supports proliferation, differentiation and extracellular matrix production of human embryonic stem cell-derived mesenchymal progenitor cells (hES-MPs) over extended time periods (up to 21 days). Cells respond positively to both chemical and mechanical stimulation of osteogenesis, with an intermittent flow profile containing rest periods strongly promoting differentiation and matrix formation in comparison to static and continuous flow. Flow and shear stresses were modeled using computational fluid dynamics. Primary cilia were detectable on cells within the device channels demonstrating that this mechanosensory organelle is present in the complex 3D culture environment. In summary, this device aids the development of 'next-generation' tools for investigating novel therapeutics for bone in comparison with standard laboratory and animal testing.
基于微流控的芯片上组织装置在生物医学应用(如药物开发)方面引起了广泛的研究兴趣,因为它们可用于对治疗剂对组织模拟物的影响进行小体积、高通量研究。芯片上组织装置正在从纳入微流控装置的基本二维细胞培养发展到复杂的三维方法,现代设计旨在重现天然组织的动态和机械环境。到目前为止,大多数芯片上组织研究都集中在参与药物摄取、代谢和清除的器官(如肺、皮肤、肝脏和肾脏);然而,药物代谢物靶器官的模型对于提供治疗效果信息至关重要。在此,我们开发了一种芯片上骨生成装置,该装置包含三维环境和流体剪切应力,这两者都是骨骼的重要特征。这种基于聚合高内相乳液(polyHIPE)的廉价、易于制造的系统能够在较长时间(长达21天)内支持人胚胎干细胞来源的间充质祖细胞(hES-MPs)的增殖、分化和细胞外基质产生。与静态和连续流动相比,细胞对成骨的化学和机械刺激均有积极反应,含有休息期的间歇流动模式强烈促进分化和基质形成。使用计算流体动力学对流动和剪切应力进行建模。在装置通道内的细胞上可检测到初级纤毛,表明这种机械感觉细胞器存在于复杂的三维培养环境中。总之,与标准实验室和动物测试相比,该装置有助于开发用于研究新型骨治疗药物的“下一代”工具。