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The chondrogenic repair response of undifferentiated mesenchymal cells in rat full-thickness articular cartilage defects.

机译:大鼠全厚度关节软骨缺损中未分化间充质细胞的软骨修复反应。

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OBJECTIVE: The aim of this study is to develop a rat model of full-thickness articular cartilage defects that is suitable for detailed molecular analyses of the regenerative repair of cartilage. MATERIALS AND METHODS: The V-shaped full-thickness defects (width: 0.7mm; depth: 0.8mm; and length: 4mm) were created in the femoral patellar groove of 6 weeks old male rats using a custom-built twin-blade device. Prior to starting the repair experiments, our device was examined for its accuracy and reliability in generating defects. Then, the time course of the repair response in these cartilage defects was examined using a semi-quantitative histological grading scale. The expression of chondrogenic differentiation markers in the reparative regions was examined with immunohistochemistry and in situ hybridization. RESULTS: Our device creates full-thickness articular cartilage defects uniformly. In these defects, undifferentiated mesenchymal cells filled the defect cavities (4 days) and initiated chondrogenic differentiation at the center of the defect (7 days). Cartilage formation was observed in the same region (2 weeks). Finally, hyaline-like articular cartilage and subchodral bone layers were reconstituted in their appropriate locations (4 weeks). CONCLUSIONS: We have successfully developed a rat model containing identically sized full-thickness defects of articular cartilage that can undergo chondrogenic repair in a reproducible fashion.
机译:目的:本研究的目的是建立全厚度关节软骨缺损的大鼠模型,该模型适用于软骨再生修复的详细分子分析。材料与方法:使用定制的双刀片装置在6周龄雄性大鼠的股骨tell槽中创建V形全层缺损(宽度:0.7mm;深度:0.8mm;长度:4mm)。 。在开始维修实验之前,我们已经检查了我们的设备在产生缺陷方面的准确性和可靠性。然后,使用半定量组织学分级量表检查这些软骨缺损中修复反应的时程。用免疫组织化学和原位杂交检测软骨形成分化标志物在修复区域中的表达。结果:我们的设备均匀地产生了全层关节软骨缺损。在这些缺损中,未分化的间充质细胞充满缺损腔(4天),并在缺损中心开始软骨生成分化(7天)。在同一区域(2周)观察到软骨形成。最后,在其适当的位置(4周)重建透明样的关节软骨和软骨下骨层。结论:我们已经成功地开发了一种大鼠模型,该模型包含相同大小的关节软骨全厚度缺损,可以以可再现的方式进行软骨修复。

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