Cementoblastic lineage formation in the cross-talk between stem cells of human exfoliated deciduous teeth and epithelial rests of Malassez cells

Clin Oral Investig. 2016 Jul;20(6):1181-91. doi: 10.1007/s00784-015-1601-6. Epub 2015 Sep 22.

Abstract

Objectives: The purpose of this study was to evaluate the synergistic effect of epithelial rests of Malassez cells (ERM) and transforming growth factor-β1 (TGF-β1) on proliferation, cementogenic and osteogenic differentiation of stem cells derived from human exfoliated deciduous teeth (SHED).

Materials and methods: SHED were co-cultured with ERM with/without TGF-β1. Then, SHED proliferation, morphological appearance, alkaline phosphatase (ALP) activity, mineralization behaviour and gene/protein expression of cemento/osteoblastic phenotype were evaluated.

Results: TGF-β1 enhanced SHED proliferation when either cultured alone or co-cultured with ERM. ERM induced the cementoblastic differentiation of SHED which was significantly accelerated when treated with TGF-β1. This activity was demonstrated by high ALP activity, strong mineral deposition and upregulation of cementum/bone-related gene and protein expressions (i.e. ALP, collagen type I, bone sialoprotein, osteocalcin and cementum attachment protein).

Conclusions: ERM were able to induce SHED differentiation along the cemento/osteoblastic lineage that was triggered in the presence of TGF-β1.

Clinical relevance: The cemento/osteoblastic differentiation capability of SHED possesses a therapeutic potential in endodontic and periodontal tissue engineering.

Keywords: Cementogenic differentiation; Epithelial rests of Malassez cells; Osteogenic differentiation; Stem cells of human exfoliated deciduous teeth; Transforming growth factor-β1.

MeSH terms

  • Cell Differentiation / physiology
  • Cell Proliferation / physiology
  • Coculture Techniques
  • Dental Cementum / cytology*
  • Dental Enamel Proteins / metabolism
  • Epithelial Cells / cytology*
  • Gene Expression
  • Humans
  • Osteogenesis / physiology*
  • Phenotype
  • Stem Cells / cytology*
  • Tooth, Deciduous / cytology*
  • Transforming Growth Factor beta1 / pharmacology

Substances

  • Dental Enamel Proteins
  • Transforming Growth Factor beta1