Department of Biomedical Science, Medical School, Foggia, Italy.
Ann N Y Acad Sci. 2011 Nov;1237:47-52. doi: 10.1111/j.1749-6632.2011.06234.x.
Dental pulp stem cells (DPSCs) are an adult stem cell population with high proliferative potential and the ability to differentiate in many cell types, and this has led scientists to consider these cells to be an alternative source of postnatal stem cells comparable to mesenchymal stem cells from bone marrow. In this work, we studied the osteoblastic phenotype developed by DPSCs cultured in osteogenic medium. In particular, we analyzed the expression of the typical osteoblast markers such as alkaline phosphatase, collagen type I, osteocalcin, osteopontin, as well as mineralized matrix production. Furthermore, the gene expression during DPSC differentiation into osteoblastic cells was studied by microarray technology. Using microarray and reverse transcriptase-polymerase chain reaction (RT-PCR) analysis, we found that IGFBP-5, JunB, and NURR1 genes are upregulated during the differentiation of DPSCs. These data indicate that opportunely differentiated DPSCs show a correct osteoblastic phenotype. Therefore, during the osteoblastic differentiation process, IGFBP-5, JunB, and NURR1 gene expression is significantly increased.
牙髓干细胞(DPSCs)是一种具有高增殖潜能和多种细胞类型分化能力的成体干细胞,这使得科学家们认为这些细胞是一种可替代的成体干细胞来源,与骨髓间充质干细胞相当。在这项工作中,我们研究了在成骨培养基中培养的 DPSCs 所表现出的成骨细胞表型。具体而言,我们分析了碱性磷酸酶、I 型胶原、骨钙素、骨桥蛋白等典型成骨细胞标志物的表达以及矿化基质的产生。此外,我们还通过微阵列技术研究了 DPSCs 向成骨细胞分化过程中的基因表达。通过微阵列和逆转录-聚合酶链反应(RT-PCR)分析,我们发现 IGFBP-5、JunB 和 NURR1 基因在 DPSCs 分化过程中上调。这些数据表明,适当分化的 DPSCs 表现出正确的成骨细胞表型。因此,在成骨细胞分化过程中,IGFBP-5、JunB 和 NURR1 基因的表达显著增加。