Effects of HEMA and TEDGMA on the in vitro odontogenic differentiation potential of human pulp stem/progenitor cells derived from deciduous teeth

被引:62
作者
Bakopoulou, Athina [2 ]
Leyhausen, Gabriele
Volk, Joachim
Tsiftsoglou, Asterios [3 ]
Garefis, Pavlos [2 ]
Koidis, Petros [2 ]
Geurtsen, Werner [1 ]
机构
[1] Hannover Med Sch, Sch Dent, Dept Conservat Dent Periodontol & Prevent Dent, D-30625 Hannover, Germany
[2] Aristotle Univ Thessaloniki, Sch Dent, Dept Fixed Prosthesis & Implant Prosthodont, Thessaloniki, Greece
[3] Aristotle Univ Thessaloniki, Sch Pharmaceut Sci, Dept Pharmacol, Thessaloniki, Greece
关键词
Resinous monomers; Biocompatibility; Stem/progenitor pulp cells; Odontogenic differentiation; Biomineralization; Reparative dentinogenesis; STEM-CELLS; RESIN MONOMERS; MAP KINASES; TEGDMA; DIMETHACRYLATE; FIBROBLASTS; ACTIVATION; EXPRESSION; TOXICOLOGY; TISSUE;
D O I
10.1016/j.dental.2011.03.002
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives. The aim of this study was to investigate the effects of HEMA and TEGDMA on the odontogenic differentiation potential of dental pulp stem/progenitor cells. Methods. Dental stem/progenitor cell cultures were established from pulp biopsies of human deciduous teeth of 1-3 year-old children (Deciduous Teeth Stem Cells-DTSCs). Cultures were characterized for stem cell markers, including STRO-1, CD146, CD34, CD45 using flow cytometry. Cytotoxicity was evaluated with the MTT assay. DTSCs were then induced for osteo/odontogenic differentiation by media containing dexamethasone, KH(2)PO(4), beta-glycerophosphate and l-ascorbic acid phosphate in the presence of nontoxic concentrations of HEMA (0.05-0.5 mM) and TEGDMA (0.05-0.25 mM) for 3 weeks. Additionally, the effects of a single exposure (72 h) to higher concentrations of HEMA (2 mM) and TEGDMA (1 mM) were also evaluated. Results. DTSCs cultures were positive for STRO-1 (7.53 +/- 2.5%), CD146 (91.79 +/- 5.41%), CD34 (11.87 +/- 3.02%) and negative for CD45. In the absence of monomers cell migration, differentiation and production of mineralized dentin-like structures could be observed. Cells also progressively expressed differentiation markers, including dentin sialophosphoprotein-DSPP, bone sialoprotein-BSP, osteocalcin-OCN and alkaline phosphatase-ALP. On the contrary, long-term exposure to nontoxic concentrations of HEMA and TEGDMA significantly delayed the differentiation and mineralization processes of DTSCs, whereas, one time exposure to higher concentrations of these monomers almost completed inhibited mineral nodule formation. BSP, OCN, ALP and DSPP expression were also significantly down-regulated. Significance. These findings suggest that HEMA and TEGDMA can severely disturb the odontogenic differentiation potential of pulp stem/progenitor cells, which might have significant consequences for pulp tissue homeostasis and repair. (C) 2011 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:608 / 617
页数:10
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