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首页> 外文期刊>Molecules >Influence of Kartogenin on Chondrogenic Differentiation of Human Bone Marrow-Derived MSCs in 2D Culture and in Co-Cultivation with OA Osteochondral Explant
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Influence of Kartogenin on Chondrogenic Differentiation of Human Bone Marrow-Derived MSCs in 2D Culture and in Co-Cultivation with OA Osteochondral Explant

机译:Kartogenin对二维培养以及与OA骨软骨移植共培养的人骨髓间充质干细胞软骨分化的影响

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Articular cartilage has limited capacity for natural regeneration and repair. In the present study, we evaluated kartogenin (KGN), a bioactive small heterocyclic molecule, for its effect on in vitro proliferation and chondrogenic differentiation of human bone marrow-derived mesenchymal stromal cells (hBMSCs) in monolayer culture and in co-culture models in vitro. OA osteochondral cylinders and hBMSCs were collected during total knee replacement. The effect of KGN on hBMSCs during 21 days of culture was monitored by real-time proliferation assay, immunofluorescence staining, histological assay, scanning electron microscopy (SEM) (imaging and multiplex enzyme-linked immunosorbent assay) ELISA assay. The rate of proliferation of hBMSCs was significantly increased by treatment with 10 μM KGN during nine days of culture. Histological and SEM analyses showed the ability of hBMSCs in the presence of KGN to colonize the surface of OA cartilage and to produce glycosaminoglycans and proteoglycans after 21 days of co-culture. KGN treated hBMSCs secreted higher concentrations of TIMPs and the secretion of pro-inflammatory molecules (MMP 13, TNF-α) were significantly suppressed in comparison with control without hBMSCs. Our preliminary results support the concept that 10 μM KGN enhances proliferation and chondrogenic differentiation of hBMSCs and suggest that KGN is a potential promoter for cell-based therapeutic application for cartilage regeneration.
机译:关节软骨的自然再生和修复能力有限。在本研究中,我们评估了生物活性小杂环分子kartogenin(KGN)在单层培养和共培养模型中对人骨髓源间充质基质细胞(hBMSCs)体外增殖和软骨分化的影响。体外。全膝关节置换期间收集了OA骨软骨圆柱体和hBMSC。通过实时增殖测定,免疫荧光染色,组织学测定,扫描电子显微镜(SEM)(成像和多重酶联免疫吸附测定)ELISA测定法监测培养21天期间KGN对hBMSC的影响。在培养的9天中,用10μMKGN处理可显着提高hBMSC的增殖速率。组织学和SEM分析显示,在共培养21天后,存在KGN的hBMSCs能够在OA软骨表面定殖并产生糖胺聚糖和蛋白聚糖的能力。与没有hBMSC的对照组相比,经KGN处理的hBMSC分泌更高浓度的TIMP,并且促炎性分子(MMP 13,TNF-α)的分泌被显着抑制。我们的初步结果支持10μMKGN增强hBMSC增殖和软骨分化的概念,并表明KGN是基于细胞的软骨再生治疗应用的潜在启动子。

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