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Hypoxia inhibits mineralization ability of human dental pulp cells treated with TEGDMA but increases cell survival in accordance with the culture time
Affiliation:1. University of Health Sciences, Gulhane Faculty of Dentistry, Department of Restorative Dentistry and Endodontics, Ankara, Turkey;2. University of Health Sciences, Gulhane Faculty of Medicine, Department of Medical Pharmacology, Ankara, Turkey;3. Gazi University, Faculty of Medicine, Department of Physiology, Ankara, Turkey;1. Genetics and Molecular Pathology, SA Pathology, North Adelaide, South Australia, Australia;2. Department of Paediatrics, The University of Adelaide, Adelaide, South Australia, Australia;3. Department of Genetics, The University of Adelaide, South Australia, Australia;4. Mesenchymal Stem Cell Laboratory, School of Medical Sciences, The University of Adelaide, Adelaide, South Australia, Australia
Abstract:ObjectiveTo evaluate the cytotoxicity and mineralization effects of TEGDMA in human dental pulp cells (hDPCs) under hypoxic and normoxic culture conditions.DesignCell viability was evaluated using XTT assay after incubation periods of 24, 48, or 72 h. The expression of mineralization-related genes (osteonectin, osteopontin, dentin sialophosphoprotein, collagen type 1) and heme oxygenase 1 (HO-1) was assessed by quantitative real-time polymerase chain reaction at 24 and 72 h.ResultsIn XTT assay, viability was higher in 0.3, 1, 2, 4, and 5 mM groups in the presence of 21% O2 after 24 h (p < 0.05). Additionally, while 0.3, 1, 2 mM groups had higher cell viability in the presence of 21% O2 after 48 h (p < 0.05), in 3 mM groups cell viability was higher under 3% O2 than 21% O2 after both 24 and 48 h (p < 0.05). 1–3 mM groups had higher cell viability under 3% O2 after 72 h (p < 0.05). There was no difference between 4 and 5 mM groups with regards to cell viability after 48 or 72 h (p > 0.05). In the gene expression study, TEGDMA-treated hDPCs showed lower mineralization potential in the presence of 3% than with 21% O2 (p < 0.05). hDPCs revealed higher HO 1 expression in 0.3 and 1 mM groups under hypoxic than under normoxic conditions after a 72-h time period (p < 0.001).ConclusionsHypoxic conditions increased cell survival in accordance with the culture period but inhibited the odontoblastic differentiation of hDPCs treated with TEGDMA.
Keywords:Cytotoxicity  Hypoxia  Mineralization  Normoxia  TEGDMA
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