In vitro osteogenic/dentinogenic potential of an experimental calcium aluminosilicate cement

J Endod. 2013 Sep;39(9):1161-6. doi: 10.1016/j.joen.2013.04.005. Epub 2013 May 16.

Abstract

Introduction: Calcium aluminosilicate cements are fast-setting, acid-resistant, bioactive cements that may be used as root-repair materials. This study examined the osteogenic/dentinogenic potential of an experimental calcium aluminosilicate cement (Quick-Set) by using a murine odontoblast-like cell model.

Methods: Quick-Set and white ProRoot MTA (WMTA) were mixed with the proprietary gel or deionized water, allowed to set completely in 100% relative humidity, and aged in complete growth medium for 2 weeks until rendered non-cytotoxic. Similarly aged Teflon disks were used as negative control. The MDPC-23 cell line was used for evaluating changes in mRNA expressions of genes associated with osteogenic/dentinogenic differentiation and mineralization (quantitative reverse transcription polymerase chain reaction), alkaline phosphatase enzyme production, and extracellular matrix mineralization (alizarin red S staining).

Results: After MDPC-23 cells were incubated with the materials in osteogenic differentiation medium for 1 week, both cements showed up-regulation in ALP and DSPP expression. Fold increases in these 2 genes were not significantly different between Quick-Set and WMTA. Both cements showed no statistically significant up-regulation/down-regulation in RUNX2, OCN, BSP, and DMP1 gene expression compared with Teflon. Alkaline phosphatase activity of cells cultured on Quick-Set and WMTA were not significantly different at 1 week or 2 weeks but were significantly higher (P < .05) than Teflon in both weeks. Both cements showed significantly higher calcium deposition compared with Teflon after 3 weeks of incubation in mineralizing medium (P < .001). Differences between Quick-Set and WMTA were not statistically significant.

Conclusions: The experimental calcium aluminosilicate cement exhibits similar osteogenic/dentinogenic properties to WMTA and may be a potential substitute for commercially available tricalcium silicate cements.

Keywords: Alizarin red S staining; MDPC-23 cells; alkaline phosphatase; calcium aluminosilicate cement; quantitative reverse transcription polymerase chain reaction.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Alkaline Phosphatase / drug effects
  • Aluminum Compounds / pharmacology
  • Aluminum Silicates / pharmacology*
  • Animals
  • Calcification, Physiologic / drug effects
  • Calcium Compounds / pharmacology*
  • Cell Culture Techniques
  • Cell Differentiation / drug effects
  • Cell Line
  • Core Binding Factor Alpha 1 Subunit / drug effects
  • Culture Media
  • Dental Cements / pharmacology*
  • Dentinogenesis / drug effects*
  • Drug Combinations
  • Extracellular Matrix / drug effects
  • Extracellular Matrix Proteins / drug effects
  • Humidity
  • Integrin-Binding Sialoprotein / drug effects
  • Materials Testing
  • Mice
  • Odontoblasts / drug effects*
  • Osteocalcin / drug effects
  • Osteogenesis / drug effects*
  • Oxides / pharmacology
  • Phosphoproteins / drug effects
  • Root Canal Filling Materials / pharmacology
  • Sialoglycoproteins / drug effects
  • Silicates / pharmacology
  • Time Factors

Substances

  • Aluminum Compounds
  • Aluminum Silicates
  • Calcium Compounds
  • Core Binding Factor Alpha 1 Subunit
  • Culture Media
  • Dental Cements
  • Dmp1 protein, mouse
  • Drug Combinations
  • Extracellular Matrix Proteins
  • Ibsp protein, mouse
  • Integrin-Binding Sialoprotein
  • Oxides
  • Phosphoproteins
  • Quick-Set
  • Root Canal Filling Materials
  • Runx2 protein, mouse
  • Sialoglycoproteins
  • Silicates
  • dentin sialophosphoprotein
  • mineral trioxide aggregate
  • Osteocalcin
  • Alkaline Phosphatase