MgO-enhanced β-TCP promotes osteogenesis in both in vitro and in vivo rat models

Sci Rep. 2024 Aug 25;14(1):19725. doi: 10.1038/s41598-024-70512-5.

Abstract

Allogeneic bone grafts are used to treat bone defects in orthopedic surgery, but the osteogenic potential of artificial bones remains a challenge. In this study, we developed a β-tricalcium phosphate (β-TCP) formulation containing MgO, ZnO, SrO, and SiO2 and compared its bone-forming ability with that of β-TCP without biological elements. We prepared β-TCP discs with 60% porosity containing 1.0 wt% of these biological elements. β-TCP scaffolds were loaded with bone marrow-derived mesenchymal stem cells (BMSC) from 7-week-old male rats and cultured for 2 weeks. ALP activity and mRNA expression of osteogenic markers were evaluated. In addition, scaffolds were implanted subcutaneously in rats and analyzed after 7 weeks. In vitro, the MgO group showed lower Ca concentrations and higher osteogenic marker expression compared to controls. In vivo, the MgO group showed higher ALP activity compared to controls, and RT-qPCR analysis showed significant expression of BMP2 and VEGF. Histopathology, fluorescent immunostaining, and micro-CT also showed relatively better bone formation in the MgO group. β-TCP with MgO may enhance bone morphology in vitro and in vivo and improve the prognosis of patients with substantial and refractory bone defects.

Keywords: Allogeneic bone grafts; Bone marrow-derived mesenchymal stem cells osteogenesis; β-tricalcium phosphate.

MeSH terms

  • Alkaline Phosphatase / metabolism
  • Animals
  • Bone Morphogenetic Protein 2 / genetics
  • Bone Morphogenetic Protein 2 / metabolism
  • Calcium Phosphates* / chemistry
  • Calcium Phosphates* / pharmacology
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Magnesium Oxide* / chemistry
  • Magnesium Oxide* / pharmacology
  • Male
  • Mesenchymal Stem Cells* / cytology
  • Mesenchymal Stem Cells* / drug effects
  • Mesenchymal Stem Cells* / metabolism
  • Osteogenesis* / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Tissue Engineering / methods
  • Tissue Scaffolds* / chemistry
  • Vascular Endothelial Growth Factor A / genetics
  • Vascular Endothelial Growth Factor A / metabolism
  • X-Ray Microtomography

Substances

  • beta-tricalcium phosphate
  • Calcium Phosphates
  • Magnesium Oxide
  • Bone Morphogenetic Protein 2
  • Alkaline Phosphatase
  • Vascular Endothelial Growth Factor A