Zeiter Stephan, Lezuo Patrick, Ito Keita
AO Research Institute, Davos, Switzerland.
Biorheology. 2009;46(1):45-55. doi: 10.3233/BIR-2009-0520.
Bioactive factors, such as TGF beta and BMP-2, as well as mechanical factors i.e. compressive loading and hydraulic pressure, have been shown to induce and/or modulate chondrogenesis of bone marrow derived mesenchymal stromal cells (BMSCs). Since these factors are intracellularly transduced through different mechanisms, it is hypothesized that TGF beta, BMP-2 and hydraulic pressure may act synergistically on chondrogenic differentiation of BMSCs. Aggregates of bovine BMSC were cultured in the presence of 10 ng/ml TGF beta1, 50 ng/ml BMP-2 or both. Half of the samples were loaded for 4 hours per day with 0.5-3 MPa cyclic hydraulic pressure at 1 Hz. After 14 days of culture/loading, gene expression of chondrogenic genes was assessed. DNA as well as glycosaminoglycan (GAG) content of the pellets were analysed. Neither pressure nor BMP-2 had an influence on GAG/DNA content. However, cells responded to the presence of TGF beta1 with an up-regulation of chondrogenic genes and GAG/DNA of the aggregates increased compared to controls demonstrating the cells ability to respond to external stimuli. The used concentrations of BMP-2 and parameters for pressure were neither able to induce nor modulate chondrogenesis of bovine BMSCs and thus no synergistic effects were observed.
生物活性因子,如转化生长因子β(TGF beta)和骨形态发生蛋白-2(BMP-2),以及机械因子,即压缩载荷和液压,已被证明可诱导和/或调节骨髓间充质基质细胞(BMSCs)的软骨形成。由于这些因子通过不同机制在细胞内转导,因此推测TGF beta、BMP-2和液压可能对BMSCs的软骨分化起协同作用。将牛BMSC聚集体在10 ng/ml TGF beta1、50 ng/ml BMP-2或两者存在的情况下进行培养。一半的样本每天以1 Hz的频率加载0.5-3 MPa的循环液压4小时。培养/加载14天后,评估软骨形成基因的基因表达。分析颗粒的DNA以及糖胺聚糖(GAG)含量。压力和BMP-2均对GAG/DNA含量没有影响。然而,细胞对TGF beta1的存在有反应,软骨形成基因上调,与对照组相比,聚集体的GAG/DNA增加,表明细胞有能力对外界刺激作出反应。所使用的BMP-2浓度和压力参数既不能诱导也不能调节牛BMSCs的软骨形成,因此未观察到协同效应。