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Size Regulation of Chondrocyte Spheroids Using a PDMS-Based Cell Culture Chip

机译:使用基于PDMS的细胞培养芯片调节软骨细胞球体的大小

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Cartilage self-repair is limited due to a lack of blood supply and the low mitosis rate of chondrocytes. A tissue engineering approach using cells and biomaterials has the potential to treat cartilage injury. Three-dimensional cellular aggregates are an excellent model for mimicking condensation and chondrogenic differentiation in vitro. We developed a technique for constructing spheroids utilizing a polydimethylsiloxane (PDMS)-based culture chip. The objective of this study is to determine how the initial cell density on a culture chip affects the chondrogenic ATDC5 cell differentiation. We demonstrate how culture chips having arrays of multicavities are able to generate high numbers of uniform spheroids rapidly and simultaneously with narrow size distribution. Spheroids are collected easily and noninvasively. Higher cell seeding density on the culture chip enhances chondrogenic cell differentiation. These results suggest the usefulness of this chip in engineering 3D cellular constructs with high functionality for tissue engineering.
机译:由于缺乏血液供应和软骨细胞的有丝分裂率低,软骨的自我修复受到限制。使用细胞和生物材料的组织工程方法具有治疗软骨损伤的潜力。三维细胞聚集体是模仿凝结和体外软骨形成分化的绝佳模型。我们开发了一种利用基于聚二甲基硅氧烷(PDMS)的培养芯片构建球体的技术。这项研究的目的是确定培养芯片上的初始细胞密度如何影响成软骨的ATDC5细胞分化。我们演示了具有多腔阵列的培养芯片如何能够快速且同时以狭窄的尺寸分布生成大量均匀的球体。球体易于收集且无创。培养芯片上较高的细胞接种密度可增强软骨细胞的分化。这些结果表明该芯片在用于组织工程的具有高功能性的工程3D细胞结构中的实用性。

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