Combination of Carbonate Hydroxyapatite and Stem Cells from Human Deciduous Teeth Promotes Bone Regeneration by Enhancing BMP-2, VEGF and CD31 Expression in Immunodeficient Mice

Cells. 2022 Jun 13;11(12):1914. doi: 10.3390/cells11121914.

Abstract

The objective of this study was to clarify the efficiency of a combination of stem cells from human deciduous teeth and carbonate apatite in bone regeneration of calvarial defects. Immunodeficient mice (n = 5 for each group/4 groups) with artificial calvarial bone defects (5 mm in diameter) were developed, and stem cells from human deciduous teeth (SHEDs) and carbonate hydroxyapatite (CAP) granules were transplanted with an atelocollagen sponge as a scaffold. A 3D analysis using microcomputed tomography, and 12 weeks after transplantation, histological and immunohistochemical evaluations of markers of bone morphogenetic protein-2 (BMP-2), vascular endothelial growth factor (VEGF), and cluster of differentiation (CD) 31 were performed. In the 3D analysis, regenerated bone formation was observed in SHEDs and CAP, with the combination of SHEDs and CAP showing significantly greater bone regeneration than that in the other groups. Histological and immunohistochemical evaluations showed that combining SHEDs and CAP enhanced the expression of BMP-2, VEGF, and CD31, and promoted bone regeneration. This study demonstrates that the combination of SHEDs and CAP transplantation may be a promising tool for bone regeneration in alveolar defects.

Keywords: bone grafting; bone morphogenetic protein-2; bone regeneration; carbonate apatite; stem cell from human deciduous teeth; vascular endothelial growth factor.

MeSH terms

  • Animals
  • Bone Morphogenetic Protein 2 / metabolism
  • Bone Regeneration
  • Carbonates
  • Durapatite* / pharmacology
  • Humans
  • Mice
  • Platelet Endothelial Cell Adhesion Molecule-1 / metabolism
  • Stem Cells / metabolism
  • Tooth, Deciduous
  • Vascular Endothelial Growth Factor A* / metabolism
  • X-Ray Microtomography

Substances

  • Bmp2 protein, mouse
  • Bone Morphogenetic Protein 2
  • Carbonates
  • Pecam1 protein, mouse
  • Platelet Endothelial Cell Adhesion Molecule-1
  • Vascular Endothelial Growth Factor A
  • Durapatite

Grants and funding

This research was funded by the Japan Society for the Promotion of Science, grant numbers 20K23055, 19K21368, 19K19269, 20K10226, and 21K10186.