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Effect of different aged cartilage ECM on chondrogenesis of BMSCs

机译:不同老年软骨ECM对BMSC软骨发生的影响

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摘要

Extracellular matrix (ECM)-based biomaterials are promising candidates in cartilage tissue engineering by simulating the native microenvironment to regulate the chondrogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) without exogenous growth factors. The biological properties of ECM scaffolds are primarily depended on the original source, which would directly influence the chondrogenic effects of the ECM materials. Despite the expanding investigations on ECM scaffolds in recent years, the selection of optimized ECM materials in cartilage regeneration was less reported. In this study, we harvested and compared the articular cartilage ECM from newborn, juvenile and adult rabbits. The results demonstrated the significant differences in the mechanical strength, sulphated glycosaminoglycan and collagen contents of the different aged ECM, before and after decellularization. Consequently, different compositional and mechanical properties were shown in the three ECM-based collagen hydrogels, which exerted age-dependent chondrogenic inducibility. In general, both in vitro and in vivo results suggested that the newborn ECM promoted the most chondrogenesis of BMSCs but led to severe matrix calcification. In contrast, BMSCs synthesized the lowest amount of cartilaginous matrix with minimal calcification with adult ECM. The juvenile ECM achieved the best overall results in promoting chondrogenesis of BMSCs and preventing matrix calcification. Together, this study provides important information to our current knowledge in the design of future ECM-based biomaterials towards a successful repair of articular cartilage.
机译:基质基质(ECM)的生物材料是通过模拟天然微环境来调节骨髓间充质干细胞(BMSC)的软骨分化而没有外源生长因子的软骨组织工程中有希望的候选物。 ECM支架的生物学性质主要依赖于原始来源,这将直接影响ECM材料的软骨性作用。尽管近年来,尽管近年来对ECM支架的调查进行了扩大,但仍报道了软骨再生中优化的ECM材料。在这项研究中,我们收获并与新生儿,少年和成人兔的关节软骨ECM进行了收获。结果表明,在脱细胞化之前和之后,不同老年ECM的机械强度,硫酸化糖胺糖苷和胶原含量的显着差异。因此,在三种ECM基胶原水凝胶中示出了不同的成分和机械性能,其施加了适应年龄依赖性的软骨内诱导性。通常,体外和体内结果表明,新生ECM促进了BMSC的最多细胞发生,但导致了严重的基质钙化。相反,BMSCs合成了用成年ECM的最小钙化量的最低量的软骨基质。青少年ECM实现了促进BMSC软骨发生和防止基质钙化的最佳结果。这项研究在一起,为我们目前的知识提供了重要信息,这些信息在未来基于ECM的生物材料设计方面,朝着成功修复关节软骨。

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