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A Study Of Crystalline Biomaterials For Articular Cartilage Bioengineering

机译:关节软骨生物工程用结晶生物材料的研究

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This study examines the suitability of marine origin coral species, Porites lutea (POR) and the hydrozoan Millepora dichotoma (MIL), for use as novel three dimensional growth matrices in the field of articular cartilage tissue engineering. Therefore, mesenchymal stem cells (MSCs) and chondrocytes were grown on the skeletal material obtained from each of these two organisms to investigate their potential use as three dimensional scaffolding for cartilage tissue growth. Chondrogenic induction of MSCs was achieved by addition of transforming growth factor-βl (TGF-β1) and insulin growth factor-I (IGF-I). Cell adherence, proliferation, differentiation and tissue development were investigated through six weeks of culture. Cartilage tissue growth and chondrocytic phenotype maintenance of each cell type were examined by cell morphology, histochemical analyses, expression of collagen type II and quantitative measures of glycosaminoglycan (GAG) content. The MSCs and the chondrocytes were shown good adherence to the scaffolds and maintenance of the chondrocytic phenotype in the initial stages of culture. However after two weeks of culture on MIL and three weeks on POR these cultures began to exhibit signs of further differentiation and phenotypic loss. The shown results indicated that POR was a better substrate for chondrocytes phenotype maintenance than MIL We believe that surface modification of POR combined with mechanical stimuli will provide a suitable environment for chondrogenic phenotype maintenance. Further investigation of POR and other novel coralline biomatrices is indicated and warranted in the field of cartilage tissue engineering applications.
机译:这项研究检查了海洋起源的珊瑚物种,Porites lutea(POR)和Hydrozoan Millepora dichotoma(MIL)的适用性,在关节软骨组织工程领域用作新型三维生长基质。因此,间充质干细胞(MSCs)和软骨细胞生长在从这两种生物中的每一种获得的骨骼材料上,以研究其作为三维支架在软骨组织生长中的潜在用途。通过添加转化生长因子-β1(TGF-β1)和胰岛素生长因子-I(IGF-1)来实现MSC的软骨诱导。经过六周的培养,研究了细胞粘附,增殖,分化和组织发育。通过细胞形态学,组织化学分析,II型胶原蛋白的表达以及糖胺聚糖(GAG)含量的定量检测,检查了每种细胞类型的软骨组织生长和软骨细胞表型维持情况。在培养的初始阶段,MSC和软骨细胞显示出对支架的良好粘附性和软骨细胞表型的维持。但是,在MIL上培养两周和在POR上培养三周后,这些培养物开始显示出进一步分化和表型丧失的迹象。显示的结果表明,POR是比MIL更好的软骨细胞表型维持底物。我们认为POR的表面修饰结合机械刺激将为软骨生成表型维持提供合适的环境。在软骨组织工程应用领域中指出并保证了对POR和其他新型珊瑚生物基质的进一步研究。

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