Hsieh Shu-Chen, Wang Fung-Fang, Lin Ching-Shih, Chen Yu-Ju, Hung Shih-Chieh, Wang Yng-Jiin
Institute of Biomedical Engineering, National Yang-Ming University, Taipei 112, Taiwan.
Biomaterials. 2006 Mar;27(8):1656-64. doi: 10.1016/j.biomaterials.2005.09.004. Epub 2005 Sep 26.
CdSe/ZnS quantum dots (QDs) have recently been used as cell tracers for long term imaging of live cells. A number of studies indicate that introduction of quantum dots to cells have no apparent deleterious effects on the morphology or growth of cells. In the present study, the human bone marrow mesenchymal stem cells (hBMSCs) were used as a model to examine the effects of QDs on the growth and osteogenic differentiation of the cells. The CdSe/ZnS QDs were delivered into hBMSCs by liposome-mediated transfection with high efficiency; analysis by transmission electron microscopy revealed that the internalized QDs could be located in the endosome-like vesicles. Uptake of QDs into hBMSCs did not affect the proliferation and cell cycle distribution of the cells. When induced to differentiate along the osteogenic lineage, the QD-containing-hBMSCs were shown to have mineral deposition on the extracellular matrix. However, the cells displayed lower alkaline phosphatase activity as compared to those without QDs. Analysis by reverse transcriptase polymerase chain reaction further demonstrated that the expression of two osteogenic markers, osteopontin and osteocalcin, was significantly inhibited. Together our results show that the presence of QDs in hBMSCs prevents the full response of the cells to induced osteogenic differentiation.
硒化镉/硫化锌量子点(QDs)最近被用作活细胞长期成像的细胞示踪剂。多项研究表明,将量子点引入细胞对细胞的形态或生长没有明显的有害影响。在本研究中,人类骨髓间充质干细胞(hBMSCs)被用作模型,以研究量子点对细胞生长和成骨分化的影响。通过脂质体介导的转染,高效地将硒化镉/硫化锌量子点导入hBMSCs;透射电子显微镜分析显示,内化的量子点可位于类似内体的囊泡中。量子点进入hBMSCs并不影响细胞的增殖和细胞周期分布。当诱导沿成骨谱系分化时,含量子点的hBMSCs显示在细胞外基质上有矿物质沉积。然而,与不含量子点的细胞相比,这些细胞的碱性磷酸酶活性较低。逆转录聚合酶链反应分析进一步表明,两种成骨标志物骨桥蛋白和骨钙素的表达受到显著抑制。我们的结果共同表明,hBMSCs中量子点的存在会阻止细胞对诱导成骨分化的完全反应。