Liu Yu Kan, Lu Qiao Zhi, Pei Rui, Ji Hui Jiao, Zhou Guo Shun, Zhao Xiao Li, Tang Rui Kang, Zhang Ming
College of Life Science, ZheJiang University, Hangzhou 310058, People's Republic of China.
Biomed Mater. 2009 Apr;4(2):025004. doi: 10.1088/1748-6041/4/2/025004. Epub 2009 Feb 11.
The aim of this study is to demonstrate the effect of extracellular calcium ion (Ca2+) and inorganic phosphate (Pi) concentrations on the growth and differentiation of bone-marrow-derived mesenchymal stem cells (MSCs), which is essential to understand the interaction between calcium phosphate ceramic (CPC) scaffolds and seeded cells during the construction of tissue-engineered bones. MSCs were separated from rabbits and cultured in media with different concentrations of Ca2+ and Pi supplements. Their proliferation, apoptosis, mineralization and osteogenic differentiation were determined by the MTT assay, TUNEL assay, Vonkossa stain and RT-PCR examination. A two-way ANOVA calculation with comparisons of estimated marginal means by LSD was used for statistical analysis. Results showed that the optimal extracellular Ca2+ and Pi concentrations for the cells to proliferate and differentiate were 1.8 mM and 0.09 mM, respectively, which are the concentrations supplied in many commonly used culture media such as DMEM and alpha-MEM. Cell proliferation and differentiation decreased significantly with greater or lower concentrations of the Pi supplement. Greater Pi concentrations also led to significant cell apoptosis. Greater Ca2+ concentrations did not change cell proliferation but significantly inhibited cell differentiation. In addition, greater Ca2+ concentrations could significantly enhance cell mineralization. In conclusion, extracellular Ca2+ and Pi significantly influence the growth and osteogenic differentiation of MSCs. It is important to take the cellular effect of Ca2+ and Pi into consideration when designing or constructing scaffolds for bone tissue engineering with CPC.
本研究的目的是证明细胞外钙离子(Ca2+)和无机磷酸盐(Pi)浓度对骨髓间充质干细胞(MSCs)生长和分化的影响,这对于理解磷酸钙陶瓷(CPC)支架与接种细胞在组织工程骨构建过程中的相互作用至关重要。从兔子体内分离出MSCs,并在添加不同浓度Ca2+和Pi的培养基中培养。通过MTT法、TUNEL法、Vonkossa染色和RT-PCR检测来确定它们的增殖、凋亡、矿化和成骨分化情况。采用双向方差分析计算,并通过LSD法比较估计边际均值进行统计分析。结果表明,细胞增殖和分化的最佳细胞外Ca2+和Pi浓度分别为1.8 mM和0.09 mM,这是许多常用培养基(如DMEM和α-MEM)中提供的浓度。Pi补充剂浓度过高或过低都会显著降低细胞增殖和分化。较高的Pi浓度也会导致显著的细胞凋亡。较高的Ca2+浓度不会改变细胞增殖,但会显著抑制细胞分化。此外,较高的Ca2+浓度可显著增强细胞矿化。总之,细胞外Ca2+和Pi显著影响MSCs的生长和成骨分化。在用CPC设计或构建骨组织工程支架时,考虑Ca2+和Pi的细胞效应很重要。