首页> 外文期刊>Journal of Surgical Research: Clinical and Laboratory Investigation >Healing of full-thickness articular cartilage defects treated with cultured autologous chondrogenic satellite cells isolated from chondral stem cell niche in rabbits
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Healing of full-thickness articular cartilage defects treated with cultured autologous chondrogenic satellite cells isolated from chondral stem cell niche in rabbits

机译:从软骨干细胞小生境分离的培养自体软骨生成卫星细胞治疗兔全层软骨缺损的愈合

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Background: Healing of articular cartilage has remained in question with the use of conventional treatment modalities such as subchondral drilling and microfracture. As demonstrated in the past, adult stem cells retain promising clonogenicity. Therefore, we conducted this study to elucidate the effects of cultured autologous chondrogenic satellite cells (CACSCs) compared with subchondral drilling (SCD) for the repair of full-thickness articular cartilage defects. Materials and methods: We examined CACSCs isolated from the knee of rabbits using flow cytometry for the expression of stemness and chondrocyte-specific factors. Subsequently, we created a full-thickness cartilage defect model with a diameter of 3 mm and depth of 2 mm on the articular surface of trochlear grooves in the left knee of 24 New Zealand white rabbits. Then we drilled subchondrally through the defect in all animals and stuffed the defects with 10-μg/cm2 collagen scaffolds. In the treatment group, we instilled CACSCs at 5 × 106 cells/mL in the collagen scaffold and collected samples on days 15, 30, and 45. Results: The CACSCs revealed significant expression of CD106, CD44, collagen type 2, and aggrecan. In conjunction with SCD, CACSCs improved healing of the articular cartilage defect, as evidenced by the formation of hyaline-like tissue grossly and histologically. The healed tissue also revealed a significant (P 0.05) increase in the expression of collagen type 2 and aggrecan (by real-time polymerase chain reaction) during the experiment. Conclusions: In conjunction with SCD, CACSCs may be considered to improve articular cartilage damage.
机译:背景:使用软骨下钻孔和微骨折等常规治疗方法治疗关节软骨仍然存在疑问。如过去所证明的,成年干细胞保留有希望的克隆形成性。因此,我们进行了这项研究,以阐明培养的自体软骨生成卫星细胞(CACSCs)与软骨下钻探(SCD)相比对全厚度关节软骨缺损的修复作用。材料和方法:我们使用流式细胞仪检查了从兔膝盖分离出的CACSCs的干性和软骨细胞特异性因子的表达。随后,我们在24只新西兰白兔的左膝滑车槽关节表面上创建了一个直径3 mm,深度2 mm的全层软骨缺损模型。然后我们在软骨下钻穿所有动物的缺损,并用10μg/ cm2胶原蛋白支架填充缺损。在治疗组中,我们以5×106细胞/ mL的剂量将CACSCs注入胶原蛋白支架中,并在第15、30和45天收集样品。结果:CACSCs显示CD106,CD44、2型胶原蛋白和聚集蛋白聚糖显着表达。与SCD结合,CACSCs可以改善关节软骨缺损的愈合,这可以通过在整体上和组织学上形成透明样组织来证明。在实验过程中,愈合的组织还显示2型胶原蛋白和聚集蛋白聚糖的表达显着(P <0.05)增加(通过实时聚合酶链反应)。结论:与SCD一起,可考虑将CACSCs改善关节软骨损伤。

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