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3D Dynamic Culture of Rabbit Articular Chondrocytes Encapsulated in Alginate Gel Beads Using Spinner Flasks for Cartilage Tissue Regeneration

机译:使用旋转瓶用于软骨组织再生的藻酸盐凝胶珠粒封装的兔关节软骨细胞的3D动态培养

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摘要

Cell-based therapy using chondrocytes for cartilage repair suffers from chondrocyte dedifferentiation. In the present study, the effects of an integrated three-dimensional and dynamic culture on rabbit articular chondrocytes were investigated. Cells (passages 1 and 4) were encapsulated in alginate gel beads and cultured in spinner flasks in chondrogenic and chondrocyte growth media. Subcutaneous implantation of the cell-laden beads was performed to evaluate the ectopic chondrogenesis. It was found that cells remained viable after 35 days in the three-dimensional dynamic culture. Passage 1 cells demonstrated a proliferative growth in both media. Passage 4 cells showed a gradual reduction in DNA content in growth medium, which was attenuated in chondrogenic medium. Deposition of glycosaminoglycans (GAG) was found in all cultures. While passage 1 cells generally produced higher amounts of GAG than passage 4 cells, GAG/DNA became similar on day 35 for both cells in growth media. Interestingly, GAG/DNA in growth medium was greater than that in chondrogenic medium for both cells. Based on GAG quantification and gene expression analysis, encapsulated passage 1 cells cultured in growth medium displayed the best ectopic chondrogenesis. Taken together, the three-dimensional and dynamic culture for chondrocytes holds great potential in cartilage regeneration.
机译:使用软骨细胞进行软骨修复的基于细胞的疗法遭受软骨细胞去分化的困扰。在本研究中,研究了整合的三维动态培养对兔关节软骨细胞的影响。将细胞(第1和第4代)封装在藻酸盐凝胶珠中,并在旋转瓶中的软骨和软骨细胞生长培养基中培养。皮下植入充满细胞的珠子,以评估异位软骨形成。发现在三维动态培养中35天后细胞仍保持活力。第1代细胞在两种培养基中均显示出增殖性生长。第4代细胞显示出生长培养基中DNA含量逐渐减少,而在软骨形成培养基中则减弱。在所有培养物中均发现了糖胺聚糖(GAG)的沉积。尽管第1代细胞通常比第4代细胞产生更高的GAG量,但对于生长培养基中的两种细胞,GAG / DNA在第35天变得相似。有趣的是,两种细胞的生长培养基中的GAG / DNA均大于软骨生成培养基中的GAG / DNA。基于GAG定量和基因表达分析,在生长培养基中培养的封装的传代1细胞表现出最佳的异位软骨形成。综上所述,软骨细胞的三维动态培养在软骨再生中具有巨大的潜力。

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