Department of Biomedical Engineering, University of California, Davis, 451 Health Sciences Drive, Davis, CA, 95616, USA.
Stem Cell Rev Rep. 2015 Jun;11(3):387-93. doi: 10.1007/s12015-014-9555-7.
Current protocols for inducing osteogenic differentiation in mesenchymal stem/stromal cells (MSCs) in culture for tissue engineering applications depend on the use of biochemical supplements. However, standard in vitro culture conditions expose cells to ambient oxygen concentrations and high levels of serum (21% O2, 10% FBS) that do not accurately recapitulate the physiological milieu. While we and others have examined MSC behavior under hypoxia, the synergistic effect of low serum levels, such as those present in ischemic injury sites, on osteogenic differentiation has not been clearly examined. We hypothesized that a concomitant reduction of serum and O2 would enhance in vitro osteogenic differentiation of MSCs by more accurately mimicking the fracture microenvironment. We show that serum deprivation, in conjunction with hypoxia, potentiates osteogenic differentiation in MSCs. These data demonstrate the role of serum levels in regulating osteogenesis and its importance in optimizing MSC differentiation strategies.
Serum levels, in addition to hypoxia, have a significant effect on MSC osteogenic differentiation. Both naïve and osteogenically induced MSCs exhibit higher osteogenic markers in reduced serum. MSCs deposit the most calcium under 5% O2 in osteogenic media supplemented with 5% FBS. Standard culture conditions (21% O2, 10% FBS) may not be optimal for MSC osteogenic differentiation.
目前,用于组织工程应用的培养中的间充质干细胞(MSCs)成骨分化的方案依赖于生化添加剂的使用。然而,标准的体外培养条件使细胞暴露于环境氧浓度和高血清水平(21%O2,10%FBS),这不能准确再现生理环境。虽然我们和其他人已经研究了低氧条件下 MSC 的行为,但低血清水平(如缺血损伤部位存在的水平)与成骨分化的协同作用尚未得到明确研究。我们假设,同时降低血清和 O2 浓度可以通过更准确地模拟骨折微环境来增强 MSC 的体外成骨分化。我们表明,血清剥夺与低氧联合作用增强了 MSCs 的成骨分化。这些数据表明了血清水平在调节成骨中的作用及其在优化 MSC 分化策略中的重要性。
除了低氧之外,血清水平对 MSC 成骨分化有显著影响。幼稚和诱导成骨的 MSC 在低血清中表现出更高的成骨标志物。在补充有 5%FBS 的成骨培养基中,5%O2 下 MSC 沉积的钙最多。标准培养条件(21%O2,10%FBS)可能不适于 MSC 成骨分化。