Tricalcium silicate cements: osteogenic and angiogenic responses of human bone marrow stem cells

Eur J Oral Sci. 2019 Jun;127(3):261-268. doi: 10.1111/eos.12613. Epub 2019 Apr 8.

Abstract

Tricalcium silicate cements (TSCs) are used in endodontic procedures to promote wound healing and hard tissue formation. The aim of this study was to evaluate and compare the effect of commonly used TSCs [mineral trioxide aggregate (MTA), Biodentine, and TotalFill] on cellular metabolism and osteogenic/angiogenic differentiation of human bone marrow mesenchymal stem cells (hBMSCs) in vitro. We tested the null hypothesis of no difference between MTA, Biodentine, and TotalFill in stem cell responses. Cells were subjected to eluates of the tested materials for up to 14 d. Cell viability was evaluated using the 3-(4,5-dimethyl-thiazoyl)-2,5-diphenyl-tetrazolium bromide (MTT) assay. Real-time PCR was used to determine the levels of expression of the osteogenic factors alkaline phosphatase (ALP), osteoprotegerin (OPG), osteocalcin (OC), and collagen 1A (COL1A1), and the angiogenic factors vascular endothelial growth factor A (VEGFA) and fibroblast growth factor 1 (FGF1). ELISAs were used to measure the levels of VEGFA and ALP in culture supernatants. Mineralization in vitro of hBMSCs was assessed using Alizarin Red staining. The hBMSCs tolerated exposure to TSCs well, with Biodentine showing the most favorable effect on cell viability. Expression of ALP, COL1A1, OPG, and VEGFA were differentially affected by the materials, with Biodentine and TotalFill inducing earlier changes at gene level. Increased mineralization was observed with time, after exposure to all TSCs tested, with MTA showing the greatest effect. The results revealed different responses of hBMSCs to TSCs in vitro.

Keywords: MTA; Biodentine; TotalFill; differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaline Phosphatase / metabolism
  • Aluminum Compounds
  • Biomineralization
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / metabolism
  • Calcium Compounds / pharmacology*
  • Cell Differentiation*
  • Cells, Cultured
  • Collagen Type I / metabolism
  • Collagen Type I, alpha 1 Chain
  • Dental Cements / pharmacology*
  • Drug Combinations
  • Fibroblast Growth Factor 1 / metabolism
  • Humans
  • Mesenchymal Stem Cells / drug effects*
  • Mesenchymal Stem Cells / metabolism
  • Osteocalcin / metabolism
  • Osteogenesis
  • Osteoprotegerin / metabolism
  • Oxides
  • Silicates / pharmacology*
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Aluminum Compounds
  • BGLAP protein, human
  • Calcium Compounds
  • Collagen Type I
  • Collagen Type I, alpha 1 Chain
  • Dental Cements
  • Drug Combinations
  • Osteoprotegerin
  • Oxides
  • Silicates
  • TNFRSF11B protein, human
  • VEGFA protein, human
  • Vascular Endothelial Growth Factor A
  • mineral trioxide aggregate
  • Fibroblast Growth Factor 1
  • Osteocalcin
  • tricalcium silicate
  • Alkaline Phosphatase