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Molecular Engineering of Arthritic Human Cartilage Ex Vivo Using Biomimetic Proteoglycans

机译:使用仿生蛋白多糖的关节炎人类软骨exVivo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可以渗入具有不同程度的OA的人关节软骨,在整个ECM中分布,并在软骨细胞周围定位。最近,我们还显示了BPG扩散在相同的结果中,在普通牛膝关节软骨前体内和常规兔膝关节软骨中的Vivo6。仿生蛋白多糖具有通过关节内注射的微创方式更换软骨ECM中的丢失的仇外心脏。通过软骨表面渗透可以用作将BPG引入关节炎软骨的方法,以分子工程师组织和恢复水合和机械性能。

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