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首页> 外文期刊>Advanced Biomedical Research >A comparative study of aggrecan synthesis between natural articular chondrocytes and differentiated chondrocytes from adipose derived stem cells in 3D culture
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A comparative study of aggrecan synthesis between natural articular chondrocytes and differentiated chondrocytes from adipose derived stem cells in 3D culture

机译:天然关节软骨细胞与脂肪衍生干细胞分化软骨细胞在3D培养中聚集蛋白聚糖合成的比较研究

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Introduction: The main obstacle for tissue engineering is to find the most appropriate cell which is able to produce extracellular matrix (ECM) similar or better than natural chondrocytes in vitro . This study compared aggrecan synthesis's potential between differentiated chondrocytes (DCs) from adipose-derived stem cells (ADSCs) and natural articular chondrocytes (NCs) in 3D culture in vitro . Materials and Methods: Human ADSCs were isolated from sub-cutaneous adipose tissue and then the surface markers including CD 14, 45 CD105, CD90, CD44 were analyzed by flow cytometry. Also human articular chondrocytes were yielded of non-weight bearing area of Knee cartilage. Both types of the cells were encapsulated in alginate scaffolds and cultured in chondrogenic medium with and without TGFβ3 for 3 weeks. Then the extent of aggercan (AGC) production was evaluated by ELISA on days 14 and 21. Results: Our findings indicated that differentiated chondrocytes (DCs) with and without TGFβ3 synthesized more AGC than natural chondrocytes (NCs) on day 14. But DCs without TGFβ3 had higher production than other groups on day 21. Application of TGFβ3 resulted in an increase of amount of AGC in DCs on day 14 but a decrease on day 21 than same group. Conclusion: Since, aggrecan is an important chondrogenic marker, it was concluded that ADSCs can be possible reliable alternative cell source for cartilage tissue engineering in future.
机译:简介:组织工程学的主要障碍是找到最合适的细胞,该细胞能够在体外产生类似于或优于天然软骨细胞的细胞外基质(ECM)。这项研究比较了体外3D培养中脂肪来源的干细胞(ADSCs)和天然关节软骨细胞(NCs)分化的软骨细胞(DCs)和聚集蛋白聚糖合成的潜力。材料与方法:从皮下脂肪组织中分离人ADSC,然后通过流式细胞仪分析包括CD 14、45 CD105,CD90,CD44在内的表面标记。同样,人关节软骨细胞产生于膝盖软骨的非承重区域。将两种类型的细胞都封装在藻酸盐支架中,并在有或没有TGFβ3的软骨形成培养基中培养3周。然后在第14天和第21天通过ELISA评估了aggercan(AGC)的产生程度。结果:我们的发现表明,在第14天,有和没有TGFβ3的分化软骨细胞(DCs)合成的AGC比天然软骨细胞(NCs)多。在第21天,TGFβ3的产量高于其他组。施用TGFβ3导致第14天DC中AGC的量增加,但在第21天与相同组相比下降。结论:由于聚集蛋白聚糖是重要的软骨形成标记,因此得出结论,ADSCs可能是将来用于软骨组织工程的可靠替代细胞来源。

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