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外源性糖胺聚糖对 II 型胶原蛋白支架培养的人软骨细胞的影响。

Effects of exogenous glycosaminoglycans on human chondrocytes cultivated on type II collagen scaffolds.

机构信息

Department of Chemical Engineering, National Tsing Hua University, 101, Section 2, Kuang-Fu Road, Hsinchu, 30013, Taiwan, ROC.

出版信息

J Mater Sci Mater Med. 2010 Feb;21(2):725-9. doi: 10.1007/s10856-009-3889-8. Epub 2009 Oct 13.

Abstract

Cartilage extracellular matrix (ECM) is composed primarily of type II collagen (COL II) and large, networks of proteoglycans (PGs) that contain glycosaminoglycans such as hyaluronic acid (HA) and chondroitin sulfate (CS). Since cartilage shows little tendency for self-repair, injuries are kept unhealed for years and can eventually lead to further degeneration. During the past decades, many investigations have pursued techniques to stimulate articular cartilage repair or regeneration. The current study assessed the effects of exogenous glycosaminoglycans (GAGs) including CS-A, CS-B, CS-C, heparan sulfate and HA, administration on human chondrocytes in terms of proliferation and matrix synthesis, while the cells were seeded and grown on the genipin-crosslinked collagen type II (COL II) scaffold. DNA content was measured by Hoechst dye intercalation, matrix deposition was evaluated by DMMB dye. Expression of collagen II and aggrecan mRNAs was assessed by RT-PCR, followed by gel electrophoresis. In a 28-day in vitro culture, administration of 5 microg/ml CS-A, 50 microg/ml CS-B, 50 microg/ml CS-C, 5 microg/ml HS, and 500 kDa HA led to significant increase in biosynthesis rate of PGs. Gene expression of aggrecan and collagen II were upregulated by CS-A, CS-C and HA. These results showed considerable relevance of GAGs to the issue of in vitro/ex vivo neo-cartilage synthesis for tissue engineering and regenerative medical applications.

摘要

软骨细胞外基质(ECM)主要由 II 型胶原(COL II)和大型蛋白聚糖(PG)网络组成,其中包含糖胺聚糖,如透明质酸(HA)和硫酸软骨素(CS)。由于软骨自我修复的倾向很小,损伤多年未愈,最终可能导致进一步退化。在过去的几十年中,许多研究都在探索刺激关节软骨修复或再生的技术。本研究评估了外源性糖胺聚糖(GAGs)包括 CS-A、CS-B、CS-C、硫酸乙酰肝素和 HA 在人软骨细胞中的增殖和基质合成作用,同时将细胞接种并在京尼平交联的 II 型胶原(COL II)支架上生长。通过 Hoechst 染料嵌入法测量 DNA 含量,通过 DMMB 染料评估基质沉积。通过 RT-PCR 评估胶原 II 和聚集蛋白聚糖 mRNAs 的表达,然后进行凝胶电泳。在 28 天的体外培养中,5μg/ml CS-A、50μg/ml CS-B、50μg/ml CS-C、5μg/ml HS 和 500kDa HA 的给药导致 PGs 生物合成率显著增加。CS-A、CS-C 和 HA 上调聚集蛋白聚糖和胶原 II 的基因表达。这些结果表明 GAGs 在组织工程和再生医学应用的体外/体外新软骨合成问题上具有相当大的相关性。

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