Effect of ProRoot MTA on pulp cell apoptosis and proliferation in vitro

J Endod. 2005 May;31(5):387-91. doi: 10.1097/01.don.0000145423.89539.d7.

Abstract

ProRoot Mineral Trioxide Aggregate (MTA) has been indicated as a pulp capping material. The purpose of this study was to evaluate the effect of tooth-colored (white) MTA on pulp cell apoptosis and cell cycle. Mouse odontoblast-like cells (MDPC-23) and undifferentiated pulp cells (OD-21) were exposed to 0 to 100 mg MTA for 24 h. Propidium iodide staining followed by flow cytometry demonstrated that MTA did not induce apoptosis of MDPC-23 or OD-21 (p > 0.05). Cell cycle analysis showed that MTA induced a modest (but significant) increase in the percentage of MDPC-23 in the S and G2 phases, and OD-21 in the S phase of cell cycle, as compared to untreated controls (p </= 0.05). In conclusion, MTA induced proliferation, and not apoptosis, of pulp cells in vitro. These findings suggest a potential mechanism to explain the regenerative effect observed in the dentin-pulp complex when MTA was used for direct pulp capping.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aluminum Compounds / pharmacology*
  • Analysis of Variance
  • Animals
  • Apoptosis / drug effects*
  • Calcium Compounds / pharmacology*
  • Cell Proliferation / drug effects*
  • Cell Survival / drug effects
  • Cells, Cultured
  • DNA Replication / drug effects
  • Dental Pulp / cytology
  • Dental Pulp / drug effects*
  • Dental Pulp Capping
  • Drug Combinations
  • Flow Cytometry
  • Materials Testing
  • Mice
  • Odontoblasts / drug effects*
  • Oxides / pharmacology*
  • Root Canal Filling Materials / pharmacology*
  • Silicates / pharmacology*

Substances

  • Aluminum Compounds
  • Calcium Compounds
  • Drug Combinations
  • Oxides
  • Root Canal Filling Materials
  • Silicates
  • mineral trioxide aggregate