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Validation of a high-throughput microtissue fabrication process for 3D assembly of tissue engineered cartilage constructs

机译:用于组织工程软骨构建体3D组装的高通量微组织制造工艺的验证

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Described here is a simple, high-throughput process to fabricate pellets with regular size and shape and the assembly of pre-cultured pellets in a controlled manner into specifically designed 3D plotted porous scaffolds. Culture of cartilage pellets is a well-established process for inducing re-differentiation in expanded chondrocytes. Commonly adopted pellet culture methods using conical tubes are inconvenient, time-consuming and space-intensive. We compared the conventional 15-mL tube pellet culture method with 96-well plate-based methods, examining two different well geometries (round- and v-bottom plates). The high-throughput production method was then used to demonstrate guided placement of pellets within a scaffold of defined pore size and geometry for the 3D assembly of tissue engineered cartilage constructs. While minor differences were observed in tissue quality and size, the chondrogenic re-differentiation capacity of human chondrocytes, as assessed by GAG/DNA, collagen type I and II immunohistochemistry and collagen type I, II and aggrecan mRNA expression, was maintained in the 96-well plate format and pellets of regular size and spheroidal shape were produced. This allowed for simple production of large numbers of reproducible tissue spheroids. Furthermore, the pellet-assembly method successfully allowed fluorescently labelled pellets to be individually visualised in 3D. During subsequent culture of 3D assembled tissue engineered constructs in vitro, pellets fused to form a coherent tissue, promoting chondrogenic differentiation and GAG accumulation.
机译:这里描述的是一种简单,高通量的方法,用于制造具有规则尺寸和形状的颗粒,以及以受控方式将预培养的颗粒组装为专门设计的3D绘制多孔支架。软骨沉淀的培养是诱导扩增的软骨细胞再分化的公认方法。常用的使用锥形管的沉淀培养方法不方便,费时且占用空间。我们将常规的15 mL管式沉淀培养方法与基于96孔板的方法进行了比较,检查了两种不同的孔几何形状(圆形和v型底部板)。然后,使用高通量生产方法来演示在组织工程软骨构建体的3D组装中,在定义的孔径和几何形状的支架中引导药丸放置。尽管在组织质量和大小上观察到微小差异,但通过GAG / DNA,I型和II型胶原免疫组织化学以及I,II型胶原和聚集蛋白聚糖mRNA表达评估的人软骨细胞的软骨再分化能力仍保持在96孔板形式和规则大小和球体形状的颗粒。这样可以简单地生产大量可复制的组织球体。此外,颗粒组装方法成功地使荧光标记的颗粒可以3D单独显示。在随后的3D组装的组织工程化体外构建物的后续培养过程中,沉淀融合形成一个连贯的组织,从而促进软骨分化和GAG积累。

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