Department of Chemical Biology, School of Pharmaceutical Sciences, Peking University Health Science Center, 38 Xueyuan Road, Beijing 100191, PR China.
Department of Chemical Biology, School of Pharmaceutical Sciences, Peking University Health Science Center, 38 Xueyuan Road, Beijing 100191, PR China.
Chem Biol Interact. 2015 Aug 5;238:111-7. doi: 10.1016/j.cbi.2015.06.027. Epub 2015 Jun 22.
In the present study, we demonstrated that calcium phosphate (CaP) nanoparticles formed in cell culture media were implicated in the process of high inorganic phosphate (Pi) mediated osteogenic differentiation of rat bone marrow stromal cells (BMSCs). Exposure of BMSCs in vitro to high Pi-containing media reduced alkaline phosphatase (ALP) activity and the expressions of osteoblast-specific genes. The sediments of CaP nanoparticles were observed at the cell surface and some of them were concomitantly found inside cells at high Pi concentration. In addition, treatment the cells with pyrophosphate (PPi), an inhibitor of calcium crystal formation, abrogated the ALP activity induced by high Pi, suggesting the contribution of CaP nanoparticles. Moreover, for isolated CaP nanoparticles, there was a trend of conversion from amorphous calcium phosphate to hydroxyapatite with elevated Pi. The particle size of CaP increased and the surface morphology changed from spherical to irregular due to increased concentrations of serum proteins incorporated into CaP nanoparticles. The study demonstrated that those physicochemical properties of CaP nanoparticles played an important role in modulating BMSCs differentiation. Furthermore, the addition of Pi in the osteogenic media resulted in a dose-dependent increase in matrix mineralization, while treatment of the cells with PPi suppressed Pi-induced calcium deposition. The findings indicated that calcium deposition in the matrix partly came from the spontaneous precipitation of CaP nanoparticles.
在本研究中,我们证明了细胞培养介质中形成的磷酸钙(CaP)纳米颗粒参与了高无机磷(Pi)介导的大鼠骨髓基质细胞(BMSCs)成骨分化过程。体外暴露于富含高 Pi 的培养基中的 BMSCs 降低了碱性磷酸酶(ALP)活性和成骨细胞特异性基因的表达。在高 Pi 浓度下,在细胞表面观察到 CaP 纳米颗粒的沉积物,其中一些同时存在于细胞内。此外,用焦磷酸盐(PPi)处理细胞,一种钙晶体形成的抑制剂,可消除高 Pi 诱导的 ALP 活性,提示 CaP 纳米颗粒的贡献。此外,对于分离的 CaP 纳米颗粒,随着 Pi 的升高,无定形磷酸钙向羟基磷灰石的转化趋势。由于血清蛋白浓度的增加,CaP 纳米颗粒的粒径增大,表面形态由球形变为不规则形。研究表明,CaP 纳米颗粒的这些物理化学性质在调节 BMSCs 分化中起着重要作用。此外,成骨培养基中添加 Pi 可导致基质矿化呈剂量依赖性增加,而用 PPi 处理细胞可抑制 Pi 诱导的钙沉积。研究结果表明,基质中的钙沉积部分来自 CaP 纳米颗粒的自发沉淀。