Biological Characteristics of Fluorescent Superparamagnetic Iron Oxide Labeled Human Dental Pulp Stem Cells.
Liang MaMing-Wei LiYu BaiHui-Hui GuoSheng-Chao WangQing YuPublished in: Stem cells international (2017)
Tracking transplanted stem cells is necessary to clarify cellular properties and improve transplantation success. In this study, we investigate the effects of fluorescent superparamagnetic iron oxide particles (SPIO) (Molday ION Rhodamine-B™, MIRB) on biological properties of human dental pulp stem cells (hDPSCs) and monitor hDPSCs in vitro and in vivo using magnetic resonance imaging (MRI). Morphological analysis showed that intracellular MIRB particles were distributed in the cytoplasm surrounding the nuclei of hDPSCs. 12.5-100 μg/mL MIRB all resulted in 100% labeling efficiency. MTT showed that 12.5-50 μg/mL MIRB could promote cell proliferation and MIRB over 100 μg/mL exhibited toxic effect on hDPSCs. In vitro MRI showed that 1 × 106 cells labeled with various concentrations of MIRB (12.5-100 μg/mL) could be visualized. In vivo MRI showed that transplanted cells could be clearly visualized up to 60 days after transplantation. These results suggest that 12.5-50 μg/mL MIRB is a safe range for labeling hDPSCs. MIRB labeled hDPSCs cell can be visualized by MRI in vitro and in vivo. These data demonstrate that MIRB is a promising candidate for hDPSCs tracking in hDPSCs based dental pulp regeneration therapy.
Keyphrases
- stem cells
- iron oxide
- magnetic resonance imaging
- contrast enhanced
- cell therapy
- induced apoptosis
- diffusion weighted imaging
- cell proliferation
- endothelial cells
- pet imaging
- cell cycle arrest
- quantum dots
- living cells
- induced pluripotent stem cells
- oxidative stress
- signaling pathway
- mesenchymal stem cells
- pluripotent stem cells
- electronic health record
- cell death
- iron oxide nanoparticles
- data analysis
- neural network
- smoking cessation
- single molecule