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Bidirectional and mutually beneficial interactions between human mesenchymal stem cells and osteoarthritic chondrocytes in micromass co-cultures

机译:人骨髓间充质干细胞与骨关节炎软骨细胞在微量共培养中的双向互利相互作用

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Aim: Mesenchymal stem cell (MSC)-based therapy presents a promising approach for treating osteoarthritis (OA). However, the molecular interactions between MSCs and OA chondrocytes (OACs) are not known. This study aims to investigate the bidirectional interactions between human MSCs (hMSCs) and human OACs (hOACs) in a 3D co-culture system. Materials & methods: hMSC-collagen microspheres were cultured in hOAC-conditioned medium or co-cultured with hOAC-collagen microspheres. Growth characteristics, glycosaminoglycan (GAG) production, gene expression of major OA-associated chondrogenic markers, including SOX9, COL2A1, ACAN and MMP13, were investigated in both cell types. Results: Both the conditioned medium and the co-culture induced MSC chondrogenesis with enhanced GAG production, SOX9 gene and protein expression, and gene expression of ACAN and COL2A1. Meanwhile, the co-culture also induced hOACs to partially resume the lost chondrogenic phenotype as shown by reduced proliferation, enhanced GAG production when hMSCs were chondrogenically predifferentiated, and reduced MMP13 gene expression. Conclusion: This work suggests that 3D co-culture of hMSCs and hOACs is mutually beneficial to each other, suggesting the potential therapeutic effect of delivering hMSC in scaffolds directly to OA defects.
机译:目的:基于间充质干细胞(MSC)的疗法为治疗骨关节炎(OA)提供了一种有前途的方法。但是,尚不知道MSC与OA软骨细胞(OAC)之间的分子相互作用。这项研究旨在调查人类MSC(hMSC)和人类OAC(hOAC)在3D共培养系统中的双向交互作用。材料与方法:将hMSC胶原微球在hOAC条件培养基中培养或与hOAC胶原微球共培养。在两种细胞类型中研究了生长特性,糖胺聚糖(GAG)的产生,与OA相关的主要软骨生成标记(包括SOX9,COL2A1,ACAN和MMP13)的基因表达。结果:条件培养基和共培养均诱导MSC软骨形成,GAG产生,SOX9基因和蛋白表达以及ACAN和COL2A1的基因表达均增强。同时,共培养还诱导hOAC部分恢复丢失的软骨原性表型,表现为增殖减少,软骨原性预分化hMSCs时GAG产生增加以及MMP13基因表达降低。结论:这项工作表明,hMSC和hOAC的3D共培养是互惠互利的,这表明将hMSC直接递送至OA缺损具有潜在的治疗作用。

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