Extracellular calcium promotes bone formation from bone marrow mesenchymal stem cells by amplifying the effects of BMP-2 on SMAD signalling

PLoS One. 2017 May 25;12(5):e0178158. doi: 10.1371/journal.pone.0178158. eCollection 2017.

Abstract

Understanding the molecular events that regulate osteoblast differentiation is essential for the development of effective approaches to bone regeneration. In this study, we analysed the osteoinductive properties of extracellular calcium in bone marrow-derived mesenchymal stem cell (BM-MSC) differentiation. We cultured BM-MSCs in 3D gelatin scaffolds with Ca2+ and BMP-2 as osteoinductive agents. Early and late osteogenic gene expression and bone regeneration in a calvarial critical-size defect model demonstrate that extracellular Ca2+ enhances the effects of BMP-2 on Osteocalcin, Runx2 and Osterix expression and promotes bone regeneration in vivo. Moreover, we analysed the molecular mechanisms involved and observed an antagonistic effect between Ca2+ and BMP-2 on SMAD1/5, ERK and S6K signalling after 24 hours. More importantly, a cooperative effect between Ca2+ and BMP-2 on the phosphorylation of SMAD1/5, S6, GSK3 and total levels of β-CATENIN was observed at a later differentiation time (10 days). Furthermore, Ca2+ alone favoured the phosphorylation of SMAD1, which correlates with the induction of Bmp2 and Bmp4 gene expression. These data suggest that Ca2+ and BMP-2 cooperate and promote an autocrine/paracrine osteogenic feed-forward loop. On the whole, these results demonstrate the usefulness of calcium-based bone grafts or the addition of exogenous Ca2+ in bone tissue engineering.

MeSH terms

  • Animals
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / physiology*
  • Bone Morphogenetic Protein 2 / physiology*
  • Calcium / pharmacology*
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology
  • Gene Expression Profiling
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / physiology*
  • Mice
  • Mice, Inbred BALB C
  • Osteoblasts / drug effects
  • Osteoblasts / physiology
  • Osteogenesis / drug effects*
  • Osteogenesis / physiology
  • Signal Transduction / drug effects*
  • Signal Transduction / physiology
  • Smad Proteins / physiology*
  • Tissue Scaffolds

Substances

  • Bmp2 protein, mouse
  • Bone Morphogenetic Protein 2
  • Smad Proteins
  • Calcium

Grants and funding

This work was supported by grants from the Ministry of Education and Science of Spain (BFU2014-56313P) and Fundació La Marató de TV3 (120330). N. Artigas received a fellowship from the University of Barcelona. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.