Gabbott C M, Zhou Z X, Han G X, Sun T
Centre for Biological Engineering, Department of Chemical Engineering, Loughborough University, Epinal Way, Loughborough, UK.
Department of Materials, Loughborough University, Epinal Way, Loughborough, UK.
J Microsc. 2017 Aug;267(2):150-159. doi: 10.1111/jmi.12555. Epub 2017 Mar 15.
At the core of translational challenges in tissue engineering is the mechanistic understanding of the underpinning biological processes and the complex relationships among components at different levels, which is a challenging task due to the limitations of current tissue culture and assessment methodologies. Therefore, we proposed a novel scale-down strategy to deconstruct complex biomatrices into elementary building blocks, which were resembled by thin modular substrate and then evaluated separately in miniaturised bioreactors using various conventional microscopes. In order to investigate cell colonisation within porous substrate in this proof-of-concept study, TEM specimen supporters (10-30 μm thick) with fine controlled open pores (100∼600 μm) were selected as the modular porous substrate and suspended in 3D printed bioreactor systems. Noninvasive imaging of human dermal fibroblasts cultured on these free-standing substrate using optical microscopes illustrated the complicated dynamic processes used by both individual and coordinated cells to bridge and segment porous structures. Further in situ analysis via SEM and TEM provided high-quality micrographs of cell-cell and cell-scaffold interactions at microscale, depicted cytoskeletal structures in stretched and relaxed areas at nanoscale. Thus this novel scaled-down design was able to improve our mechanistic understanding of tissue formation not only at single- and multiple-cell levels, but also at micro- and nanoscales, which could be difficult to obtain using other methods.
组织工程中转化挑战的核心在于对基础生物学过程以及不同层次组件之间复杂关系的机理理解,由于当前组织培养和评估方法的局限性,这是一项具有挑战性的任务。因此,我们提出了一种新颖的缩小规模策略,将复杂的生物基质解构为基本构建块,这些构建块由薄的模块化基质模拟,然后在小型生物反应器中使用各种传统显微镜分别进行评估。在这项概念验证研究中,为了研究细胞在多孔基质内的定殖情况,选择了具有精细控制的开放孔隙(100∼600μm)的TEM标本支撑物(10 - 30μm厚)作为模块化多孔基质,并悬浮在3D打印的生物反应器系统中。使用光学显微镜对在这些独立基质上培养的人真皮成纤维细胞进行非侵入性成像,展示了单个细胞和协同细胞用于连接和分割多孔结构的复杂动态过程。通过SEM和TEM进行的进一步原位分析提供了微观尺度下细胞 - 细胞和细胞 - 支架相互作用的高质量显微照片,描绘了纳米尺度下拉伸和松弛区域的细胞骨架结构。因此,这种新颖的缩小规模设计不仅能够在单细胞和多细胞水平,而且能够在微观和纳米尺度上提高我们对组织形成的机理理解,而使用其他方法可能难以获得这些信息。