SHED differentiate into functional odontoblasts and endothelium

J Dent Res. 2010 Aug;89(8):791-6. doi: 10.1177/0022034510368647. Epub 2010 Apr 15.

Abstract

Studies on mechanisms underlying the differentiation of dental pulp stem cells are critical for the understanding of the biology of odontogenesis and for dental tissue engineering. Here, we tested the hypothesis that stem cells from exfoliated deciduous teeth (SHED) differentiate into functional odontoblasts and endothelial cells. SHED were seeded in tooth slice/scaffolds and implanted subcutaneously into immunodeficient mice. SHED differentiated into functional odontoblasts that generated tubular dentin, as determined by tetracycline staining and confocal microscopy. These cells also differentiated into vascular endothelial cells, as determined by beta-galactosidase staining of LacZ-tagged SHED. In vitro, vascular endothelial growth factor (VEGF) induced SHED to express VEGFR2, CD31, and VE-Cadherin (markers of endothelium) and to organize into capillary-like sprouts. VEGF induced ERK and AKT phosphorylation (indicative of differentiation), while inhibiting phosphorylation of STAT3 (indicative of 'stemness'). Collectively, this work demonstrates that SHED can differentiate into angiogenic endothelial cells and odontoblasts capable of generating tubular dentin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult Stem Cells / cytology*
  • Animals
  • Cell Differentiation
  • Cells, Cultured
  • Dental Pulp / cytology*
  • Dentin / metabolism*
  • Endothelial Cells / cytology
  • Endothelial Cells / drug effects
  • Endothelium, Vascular / cytology*
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / metabolism
  • Extracellular Matrix Proteins / biosynthesis
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Humans
  • Mice
  • Mice, SCID
  • Neovascularization, Physiologic / physiology*
  • Odontoblasts / cytology*
  • Odontoblasts / drug effects
  • Odontoblasts / metabolism
  • Phosphoproteins / biosynthesis
  • Phosphorylation
  • Proto-Oncogene Proteins c-akt / metabolism
  • Recombinant Proteins / pharmacology
  • STAT3 Transcription Factor / metabolism
  • Sialoglycoproteins / biosynthesis
  • Subcutaneous Tissue
  • Tissue Scaffolds
  • Tooth, Deciduous / cytology
  • Vascular Endothelial Growth Factor A / pharmacology
  • Vascular Endothelial Growth Factor Receptor-1 / physiology

Substances

  • DMP1 protein, human
  • Extracellular Matrix Proteins
  • Phosphoproteins
  • Recombinant Proteins
  • STAT3 Transcription Factor
  • Sialoglycoproteins
  • Vascular Endothelial Growth Factor A
  • dentin sialophosphoprotein
  • Vascular Endothelial Growth Factor Receptor-1
  • Proto-Oncogene Proteins c-akt
  • Extracellular Signal-Regulated MAP Kinases