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Development of Cartilaginous Tissue in Chondrocyte-Agarose Construct Cultured under Traction Loading

机译:牵引载荷培养的软骨细胞 - 琼脂糖构建体中的软骨组织

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In this study, chondrocytes isolated from bovine cartilage tissue were seeded in agarose gel and resultant chondrocyte-agarose constructs, a well-established experimental model to examine the effect of mechanical loadings on the chondrocyte metabolism, were cultured with a traction loading on the construct surface to examine its effect on the regeneration of the cartilaginous tissue by chondrocytes. Custom-designed mechanical loading equipment was developed to apply the traction loading on the upper surface of constructs being cultured in the CO2 incubator. After 2 or 3 weeks culture, quantities of glycosaminoglycan (GAG) molecules that proteoglycan, and type II collagen were determined, and im-munofluorescent staining of keratin sulfate, a type of GAG, and type II collagen was performed to verify the chondrocyte biosynthesis of extra cellular matrix (ECM) and characterize the structure of elaborated cartilaginous tissue by confocal laser scanning microscopy (CLSM). Results indicated that the traction loading enhance ECM biosynthesis in the surface region of constructs and collagen rich layer covered with GAG rich superficial layer was formed in the articulation surface. Results of quantification for ECM molecules indicated that the production of type II collagen and GAG was more significant outside the slide track compared with inside the slide track.
机译:在本研究中,从雄软骨组织中分离的软骨细胞在琼脂糖凝胶中接种,并得到的软骨细胞 - 琼脂糖构建体,是一种熟悉的实验模型,以检查机械载荷对软骨细胞代谢的影响,用构建表面牵引负载培养通过软骨细胞来检查其对软骨组织再生的影响。开发了定制设计的机械装载设备以将牵引载荷应用于CO 2培养箱中培养的构建体上。在培养2或3周后,测定蛋白多糖和II型胶原蛋白酶(GAG)分子的量,并进行硫酸异杂丁,一种GAG和II型胶原蛋白的IM-Munoforcent染色,以验证软骨细胞生物合成额外的细胞基质(ECM)并通过共聚焦激光扫描显微镜(CLSM)表征阐述的软骨组织的结构。结果表明,在铰接表面中形成牵引载荷增强在构建体的表面区域和富含GAG富浅表层覆盖的富胶层的富胶层的ECM生物合成。 ECM分子量化结果表明,与滑轨内部的滑轨外部的II型胶原和GAG的产生更为显着。

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