Laboratory for Skeletal Development and Joint Disorders, Katholieke Universiteit Leuven, Leuven, Belgium.
Tissue Eng Part A. 2011 Apr;17(7-8):1083-97. doi: 10.1089/ten.TEA.2010.0160. Epub 2011 Jan 16.
The use of calcium phosphate (CaP)-based carriers in bone engineering is a promising approach to induce in vivo bone formation. However, the exact mechanism of osteoinduction by CaP is not known. Here, by mimicking the in vivo Ca(2+) and P(i)-enriched environment in an in vitro model, we assessed the effects of these ions on human periosteum-derived cells. We observed a significant Ca(2+) and P(i)-induced cell proliferation, which was found to be through the modulation of cell cycle progression, in a dose- and time-dependent manner. In addition, Ca(2+), P(i), and combined Ca-P upregulated osteogenic gene expression in a dose- and time-dependent manner. Encouragingly, both ions administered individually or in combination persistently and dose dependently upregulated bone morphogenetic protein-2 gene expression. This suggested a potential osteoinductive effect through an autonomous activation of the bone morphogenetic protein signaling pathway by released Ca(2+) and P(i), which may serve as an autocrine/paracrine osteoinduction loop that drives the cellularized CaP constructs toward effective bone formation in vivo. In conclusion, through an in vitro biomimetic model, we have partially probed the roles of the released Ca(2+) and P(i) on the osteoinductivity of CaP-based biomaterials.
使用磷酸钙(CaP)基载体进行骨工程是一种很有前途的方法,可以诱导体内骨形成。然而,CaP 诱导成骨的确切机制尚不清楚。在这里,我们通过模拟体内富含 Ca(2+)和 P(i)的环境,在体外模型中评估了这些离子对人骨膜来源细胞的影响。我们观察到 Ca(2+)和 P(i)的浓度依赖性和时间依赖性诱导细胞增殖,这是通过细胞周期进程的调节实现的。此外,Ca(2+)、P(i)和复合 Ca-P 以剂量和时间依赖性方式上调成骨基因表达。令人鼓舞的是,单独或联合施用两种离子均可持续且剂量依赖性地上调骨形态发生蛋白-2 基因表达。这表明通过释放的 Ca(2+)和 P(i)自主激活骨形态发生蛋白信号通路,可能存在潜在的成骨诱导作用,这可能是一个自分泌/旁分泌成骨诱导环路,驱动细胞化的 CaP 构建体向体内有效的骨形成。总之,通过体外仿生模型,我们部分探测了释放的 Ca(2+)和 P(i)在 CaP 基生物材料成骨活性中的作用。