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In vitro investigation and biomechanical modeling of the effects of PLF-68 on osteoarthritis in a three-dimensional model

机译:三维模型中PLF-68对骨关节炎影响的体外研究和生物力学建模

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In this study, it was hypothesized that Pluronic F-68 (PLF-68) increases matrix synthesis of osteoarthritis (OA) chondrocytes in addition to its well-documented cell survival effect. To test this hypothesis, rat articular chondrocytes were embedded in agarose discs and were exposed to 5-azacytidine (Aza-C) to induce OA-like alterations. Chondrocytes were then treated with PLF-68 (8 and 12 mg/ml) for 10 days. Aza-C-exposed and PLF-68-untreated chondrocytes and Aza-C-unexposed and PLF-68-untreated chondrocytes were used as negative and positive control groups, respectively. Dynamic hydrostatic pressure (max 0.2MPa, 0.1Hz) was applied to discs for 30min/day (5 days/week). Cell viability, collagen and proteoglycan deposition in discs were determined. Unconfined compression stress relaxation tests were performed to determine peak stress and material parameters of discs-namely spring constants (k1 and k2), damping coefficient (η), instantaneous modulus (E_0) and relaxed modulus (E_∞) using Kelvin model to evaluate the functional coherence of the matrix. PLF-68 treatment significantly increased the collagen deposition in discs and viability of OA-like chondrocytes. A dose-dependent increase was also observed for elastic stiffness parameters (k1, k2, E _0 and E_∞). Same positive effect of PLF-68 was not observed for proteoglycan deposition. However, dose-dependent increase in. suggests that PLF-68 treatment resulted with the deposition of functional matrix. This is the first study which reports that PLF-68 has also positive effect on collagen synthesis of OA cells. As a conclusion, our results suggest that PLF-68 has a potential for recovery from OA-like alterations, which should be further analyzed.
机译:在这项研究中,假设Pluronic F-68(PLF-68)除了有良好的细胞存活作用外,还可以增加骨关节炎(OA)软骨细胞的基质合成。为了检验该假设,将大鼠关节软骨细胞包埋在琼脂糖盘中,并暴露于5-氮杂胞苷(Aza-C)以诱导OA样改变。然后将软骨细胞用PLF-68(8和12 mg / ml)处理10天。暴露于Aza-C和未经PLF-68的软骨细胞和未经Aza-C暴露于PLF-68的软骨细胞分别用作阴性和阳性对照组。向圆盘施加动态静水压力(最大0.2MPa,0.1Hz)30分钟/天(5天/周)。确定圆盘中的细胞活力,胶原蛋白和蛋白聚糖沉积。使用Kelvin模型进行无边压缩应力松弛测试,以确定圆盘的峰值应力和材料参数,即弹簧常数(k1和k2),阻尼系数(η),瞬时模量(E_0)和松弛模量(E_∞)。矩阵的功能一致性。 PLF-68处理可显着增加椎间盘中的胶原蛋白沉积和OA样软骨细胞的活力。弹性刚度参数(k1,k2,E_0和E_∞)也观察到剂量依赖性增加。对于蛋白多糖沉积,未观察到PLF-68的相同阳性作用。然而,剂量依赖性增加提示PLF-68治疗是由于功能性基质的沉积而导致的。这是第一项报道PLF-68对OA细胞胶原合成也有积极作用的研究。结论是,我们的结果表明PLF-68具有从OA样改变中恢复的潜力,应进一步分析。

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