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Molecular Engineering of Arthritic Human Cartilage Ex Vivo Using Biomimetic Proteoglycans

机译:使用仿生蛋白聚糖体外进行关节炎人类软骨的分子工程。

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Conclusions: We have demonstrated that BPGs can infiltrate into human articular cartilage with varying degrees of OA, distribute throughout the ECM, and localize around the chondrocytes. Recently, we have also shown BPG diffusion following the same results in normal bovine knee cartilage ex vivo and normal rabbit knee cartilage in vivo6. Biomimetic proteoglycans have the potential to replace lost aggrecan in the cartilage ECM in a minimally invasive manner through intra-articular injections. Infiltration through the cartilage surface may serve as a method to introduce BPGs into arthritic cartilage to molecularly engineer the tissue and restore hydration and mechanical properties.
机译:结论:我们已经证明BPG可以以不同程度的OA渗入人体关节软骨,分布在整个ECM中,并位于软骨细胞周围。最近,我们还显示出BPG在正常牛膝关节软骨离体和正常兔膝关节软骨体内扩散后的结果相同6。仿生蛋白聚糖具有通过关节内注射以微创方式替代软骨ECM中失去的聚集蛋白聚糖的潜力。通过软骨表面的浸润可以用作将BPG引入关节炎软骨中以对组织进行分子工程改造并恢复水合作用和机械性能的方法。

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