加入透明质酸的鹿角储备间充质细胞可减轻大鼠软骨损伤

Boyin Jia, Xin Li, Xintong Han, Fuquan Ma, Linlin Zhang, Xue Wang, Xinrui Yan, Yu Zhang, Jianming Li, Pengfei Hu, Yusu Wang, Naichao Diao, Kun Shi, Ying Zong, Rui Du, Chunyi Li
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摘要

鹿角的储备间充质细胞(RMCs)被认为是修复损伤诱导的关节软骨或软骨变性的有希望的细胞来源。然而,RMC分化修复损伤软骨及其与生物材料结合的系统研究尚未见报道。本研究的目的是通过模拟自然环境来评估RMCs与透明质酸(HA)联合促进软骨分化的作用及其在关节软骨修复中的功效。我们在体外培养RMCs,对这些细胞进行表征,包括形态学、表面标记物表达和多能分化潜能(脂肪生成、软骨形成和成骨)。在体外与HA联合使用时,RMCs增加了软骨生成标记基因(COL II和COMP)的表达水平,但降低了增生性标记基因(COL X)的表达水平。通过大鼠关节软骨缺损模型,我们通过宏观、组织学和免疫组织化学检查,评估了RMCs与HA联合使用在第4周和第8周时对软骨缺损修复的影响。与其他组相比,RMCs + HA治疗可减少软骨损失和软骨表面磨损程度,软骨含量显著增加。这些结果表明RMCs与HA结合可以有效修复软骨缺损。我们相信有效的软骨缺损修复将受益于rmc和有利的生物材料,如透明质酸。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Deer antler reserve mesenchyme cells with hyaluronan alleviates cartilage damage in a rat model

Reserve mesenchyme cells (RMCs) of deer antlers have been considered as the promising cell source for repairing injury-induced articular cartilage or cartilage degeneration. However, systematic investigation of RMC differentiation to repair injured cartilage and its combination with biomaterials has not been reported. The aim of this study was to evaluate the role of RMCs in combination with hyaluronic acid (HA) in promoting chondrogenic differentiation through simulating native environments and their efficacy in articular cartilage repair. The RMCs were cultured in vitro for the characterization of these cells, including morphology, surface marker expression, and multipotent differentiation potential (adipogenesis, chondrogenesis, and osteogenesis). When combined with HA in vitro, RMCs increased expression levels of the chondrogenic marker gene (COL II and COMP) but decreased levels of the hypertrophic marker gene (COL X). Using a rat articular cartilage defect model, we evaluated the effects of RMCs in combination with HA on cartilage defect repair at 4 and 8 weeks through macroscopical, histological, and immunohistochemical examinations. Compared with other groups, treatment with RMCs + HA reduced cartilage loss and degree of cartilage surface worn, whereas cartilage content was significantly increased. These results suggest that the combination of RMCs with HA can effectively repair cartilage defects. We believe that effective cartilage defect repair will benefit from the use of RMCs together with favorable biomaterials, such as HA.

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