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Utility of direct 3D co-culture model for chondrogenic differentiation of mesenchymal stem cells on hyaluronan scaffold (Hyaff-11)

机译:透明质酸山丘岩手(Hyaff-11)中间充质干细胞软骨切细胞软骨分化的直接三维共培养模型

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摘要

This study presents direct 2D and 3D co-culture model of mesenchymal stem cells (MSCs) line with chondrocytes isolated from patients with osteoarthritis (unaffected area). MSCs differentiation into chondrocytes after 14, 17 days was checked by estimation of collagen I, II, X, aggrecan expression using immunohistochemistry. Visualization, localization of cells on Hyaff-11 was performed using enzymatic technique and THUNDER Imaging Systems. Results showed, that MSCs/chondrocytes 3D co-culture induced suitable conditions for chondrocytes grow and MSCs differentiation than 2D monoculture. Despite that differentiated cells on Hyaff-11 expressed collagen X, they showed high collagen II (80%) and aggrecan (60%) expression with simultaneous decrease of collagen I expression (10%). The high concentration of differentiated cells on Hyaff-11, indicate that this structure has an impact on cells cooperation and communication. In conclusion, we suggest that high expression of collagen II and aggrecan in 3D co-culture model, indicate that cooperation between different subpopulations may have synergistic impact on MSCs chondrogenic potential. Revealed the high concentration and localization of cells growing in deeper layers of membrane in 3D co-culture, indicate that induced microenvironmental enhance cell migration within scaffold. Additionally, we suggest that co-culture model might be useful for construction a bioactive structure for cartilage tissue regeneration.
机译:本研究呈现了间充质干细胞(MSCs)系列的直接2D和3D共培养模型,与骨关节炎(未受影响区域)分离的软骨细胞分离的软骨细胞。通过使用免疫组织化学估计,通过估计胶原I,II,X,Eggrecan表达,检查17天后的MSC分化为细胞细胞。可视化,使用酶促技术和雷电成像系统进行HYAFF-11上的细胞的定位。结果表明,MSCs / Chondrocytes 3D共培养诱导的软骨细胞生长和MSCs分化的合适条件高于2D单一栽培。尽管苏达11表达胶原蛋白X上的差异化细胞,但它们显示出高胶原II(80%)和聚集体(60%)表达,同时降低胶原蛋白I表达(10%)。 Hyaff-11上的高浓度分化细胞表明该结构对细胞合作和通信产生了影响。总之,我们建议在3D共培养模型中表明胶原II和聚集体的高表达,表明不同亚步骤之间的合作可能对MSC软骨形成潜力具有协同影响。揭示了3D共培养中膜更深层次的细胞的高浓度和定位,表明诱导微环境增强支架内的细胞迁移。此外,我们表明共培养模型对于构建软骨组织再生的生物活性结构可能是有用的。

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