Restor Dent Endod.  2015 Nov;40(4):290-298. 10.5395/rde.2015.40.4.290.

Effect of dentin treatment on proliferation and differentiation of human dental pulp stem cells

Affiliations
  • 1Department of Conservative Dentistry, Yonsei University College of Dentistry, Seoul, Korea. juen@yuhs.ac
  • 2Department of Advanced General Dentistry, Oral Science Research Center, Yonsei University College of Dentistry, Seoul, Korea.

Abstract


OBJECTIVES
Sodium hypochlorite (NaOCl) is an excellent bactericidal agent, but it is detrimental to stem cell survival, whereas intracanal medicaments such as calcium hydroxide (Ca[OH]2) promote the survival and proliferation of stem cells. This study evaluated the effect of sequential NaOCl and Ca[OH]2 application on the attachment and differentiation of dental pulp stem cells (DPSCs).
MATERIALS AND METHODS
DPSCs were obtained from human third molars. All dentin specimens were treated with 5.25% NaOCl for 30 min. DPSCs were seeded on the dentin specimens and processed with additional 1 mg/mL Ca[OH]2, 17% ethylenediaminetetraacetic acid (EDTA) treatment, file instrumentation, or a combination of these methods. After 7 day of culture, we examined DPSC morphology using scanning electron microscopy and determined the cell survival rate with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. We measured cell adhesion gene expression levels after 4 day of culture and odontogenic differentiation gene expression levels after 4 wk using quantitative real-time polymerase chain reaction.
RESULTS
DPSCs did not attach to the dentin in the NaOCl-treated group. The gene expression levels of fibronectin-1 and secreted phosphoprotein-1 gene in both the Ca[OH]2- and the EDTA-treated groups were significantly higher than those in the other groups. All Ca[OH]2-treated groups showed higher expression levels of dentin matrix protein-1 than that of the control. The dentin sialophosphoprotein level was significantly higher in the groups treated with both Ca[OH]2 and EDTA.
CONCLUSIONS
The application of Ca[OH]2 and additional treatment such as EDTA or instrumentation promoted the attachment and differentiation of DPSCs after NaOCl treatment.

Keyword

Calcium hydroxide; Cell attachment; Cell differentiation; Dental pulp stem cells; Regenerative endodontics; Sodium hypochlorite

MeSH Terms

Calcium Hydroxide
Cell Adhesion
Cell Differentiation
Cell Survival
Dental Pulp*
Dentin*
Edetic Acid
Gene Expression
Humans*
Microscopy, Electron, Scanning
Molar, Third
Real-Time Polymerase Chain Reaction
Sodium Hypochlorite
Stem Cells*
Calcium Hydroxide
Edetic Acid
Sodium Hypochlorite

Figure

  • Figure 1 Experimental groups for the attachment and differentiation of dental pulp stem cells. Cell attachment analysis with 3-(4,5-dimethylthiazol-2yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay (tetrazolium-based colorimetric assay).

  • Figure 2 Cell viability analysis with MTT assay. Cells in the control group were grown on plates. Data were obtained from 3 separate experiments. MTT assay, 3-(4,5-dimethylthiazol-2yl)-2,5-diphenyl-2H-tetrazolium bromide assay.

  • Figure 3 Expression levels of (a) fibronectin-1 (FN-1), and (b) secreted phosphoprotein-1 (SPP-1). Data were obtained from 3 separate experiments. *Mann-Whitney U test, level of statistical significance was set at p < 0.05.

  • Figure 4 Scanning electron microscopic views of dental pulp stem cell morphology on dentin surfaces after 7 days of culture. (a) group 2; (b) group 3; (c) group 4; (d) group 5 (magnification, ×1,000).

  • Figure 5 Expression levels of (a) dentin matrix protein-1 (DMP-1), and (b) dentin sialophosphoprotein (DSPP). Data were obtained from 3 separate experiments. *Mann-Whitney U test, level of statistical significance was set at p < 0.05.


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