1. Effects of a novel light-curable material on odontoblastic differentiation of human dental pulp cells.
- Author
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Lee BN, Lee BG, Chang HS, Hwang YC, Hwang IN, and Oh WM
- Subjects
- Alkaline Phosphatase genetics, Calcification, Physiologic drug effects, Drug Combinations, Extracellular Matrix Proteins genetics, Gene Expression drug effects, Humans, Phosphoproteins genetics, RNA, Messenger genetics, Real-Time Polymerase Chain Reaction, Reverse Transcriptase Polymerase Chain Reaction, Sialoglycoproteins genetics, Aluminum Compounds pharmacology, Calcium Compounds pharmacology, Cell Differentiation drug effects, Dental Pulp cytology, Odontoblasts drug effects, Oxides pharmacology, Silicates pharmacology
- Abstract
Aim: To assess the biological effects, including odontoblastic differentiation of a novel light-curable material (TheraCal), on human dental pulp cells (hDPCs)., Methodology: The hDPCs were isolated from freshly extracted, caries-free third molars. Ten discs of TheraCal and MTA (8 mm in diameter and 3 mm in height) were incubated in α-minimum essential medium (α-MEM) and the supernatant collected. Viability of hDPCs in response to TheraCal and MTA was measured using the WST-1 assay. RT-PCR and real-time PCR were used to detect the gene expression of dentine sialophosphoprotein (DSPP) and dentine matrix protein-1 (DMP-1). ALP staining and Alizarin red S staining were used to evaluate the expression of alkaline phosphatase (ALP) and mineralization behaviour. One-way analysis of variance and Tukey's post hoc test were used to determine the statistically significant differences as a result of the variation in test materials (P < 0.05)., Results: The effects of TheraCal and MTA on cell viability were similar except at the highest concentration. The mRNA level of DSPP increased significantly in the MTA group relative to the control at day 1 and 3 (P < 0.05). Also, the mRNA level of DSPP increased significantly in the TheraCal group relative to the control at day 3 (P < 0.05). The increased mRNA level of DMP-1 was 2.5-fold and 2.3-fold each in the MTA and TheraCal groups relative to the control (P < 0.05). Cells exposed to MTA exhibited a 1.4-fold increase of ALP staining relative to control (P < 0.05). In the mineralization assay, increased calcium nodule formation was twofold and 1.3-fold each in the MTA and TheraCal groups compared to the control (P < 0.05)., Conclusions: TheraCal and MTA had the ability to induce odontoblastic differentiation and mineralization of hDPCs., (© 2016 International Endodontic Journal. Published by John Wiley & Sons Ltd.)
- Published
- 2017
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