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Fabrication of multi-well chips for spheroid cultures and implantable constructs through rapid prototyping techniques

机译:通过快速原型技术制造用于球体培养和可植入构建体的多孔芯片

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摘要

Three-dimensional (3D) culture models are widely used in basic and translational research. In this study, to generate and culture multiple 3D cell spheroids, we exploited laser ablation and replica molding for the fabrication of polydimethylsiloxane (PDMS) multi-well chips, which were validated using articular chondrocytes (ACs). Multi-well ACs spheroids were comparable or superior to standard spheroids, as revealed by glycosaminoglycan and type-II collagen deposition. Moreover, the use of our multi-well chips significantly reduced the operation time for cell seeding and medium refresh. Exploiting a similar approach, we used clinical-grade fibrin to generate implantable multi-well constructs allowing for the precise distribution of multiple cell types. Multi-well fibrin constructs were seeded with ACs generating high cell density regions, as shown by histology and cell fluorescent staining. Multi-well constructs were compared to standard constructs with homogeneously distributed ACs. After 7 days in vitro, expression of SOX9, ACAN, COL2A1, and COMP was increased in both constructs, with multi-well constructs expressing significantly higher levels of chondrogenic genes than standard constructs. After 5 weeks in vivo, we found that despite a dramatic size reduction, the cell distribution pattern was maintained and glycosaminoglycan content per wet weight was significantly increased respect to pre-implantation samples. In conclusion, multi-well chips for the generation and culture of multiple cell spheroids can be fabricated by low-cost rapid prototyping techniques. Furthermore, these techniques can be used to generate implantable constructs with defined architecture and controlled cell distribution, allowing for in vitro and in vivo investigation of cell interactions in a 3D environment.
机译:三维(3D)文化模型广泛用于基础研究和转化研究。在这项研究中,要生成和培养多个3D细胞球体,我们利用激光烧蚀和复制模制技术制造了聚二甲基硅氧烷(PDMS)多孔芯片,并通过关节软骨细胞(AC)对其进行了验证。正如糖胺聚糖和II型胶原沉积所显示的,多孔AC球体与标准球体相当或更好。而且,使用我们的多孔芯片显着减少了细胞接种和培养基刷新的操作时间。利用类似的方法,我们使用了临床级的纤维蛋白来生成可植入的多孔结构,从而可以精确分配多种细胞类型。如组织学和细胞荧光染色所示,将多孔纤维蛋白构建物接种到产生高细胞密度区域的AC上。将多孔构建体与具有均匀分布AC的标准构建体进行比较。体外培养7天后,两种构建体中SOX9,ACAN,COL2A1和COMP的表达均增加,其中多孔构建体表达的软骨生成基因水平明显高于标准构建体。体内5周后,我们发现尽管尺寸显着减小,但相对于植入前样品,细胞分布模式仍保持不变,每湿重的糖胺聚糖含量显着增加。总之,可以通过低成本快速原型技术制造用于多细胞球体生成和培养的多孔芯片。此外,这些技术可用于生成具有定义的架构和受控的细胞分布的可植入构建体,从而可以在3D环境中进行细胞相互作用的体外和体内研究。

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