Graphene Oxide-Copper Nanocomposite-Coated Porous CaP Scaffold for Vascularized Bone Regeneration via Activation of Hif-1α

Adv Healthc Mater. 2016 Jun;5(11):1299-309. doi: 10.1002/adhm.201500824. Epub 2016 Mar 4.

Abstract

Graphene has been studied for its in vitro osteoinductive capacity. However, the in vivo bone repair effects of graphene-based scaffolds remain unknown. The aqueous soluble graphene oxide-copper nanocomposites (GO-Cu) are fabricated, which are used to coat porous calcium phosphate (CaP) scaffolds for vascularized bone regeneration. The GO-Cu nanocomposites, containing crystallized CuO/Cu2 O nanoparticles of ≈30 nm diameters, distribute uniformly on the surfaces of the porous scaffolds and maintain a long-term release of Cu ions. In vitro, the GO-Cu coating enhances the adhesion and osteogenic differentiation of rat bone marrow stem cells (BMSCs). It is also found that by activating the Erk1/2 signaling pathway, the GO-Cu nanocomposites upregulate the expression of Hif-1α in BMSCs, resulting in the secretion of VEGF and BMP-2 proteins. When transplanted into rat with critical-sized calvarial defects, the GO-Cu-coated calcium phosphate cement (CPC) scaffolds (CPC/GO-Cu) significantly promote angiogenesis and osteogenesis. Moreover, it is observed via histological sections that the GO-Cu nanocomposites are phagocytosed by multinucleated giant cells. The results suggest that GO-Cu nanocomposite coatings can be utilized as an attractive strategy for vascularized bone regeneration.

Keywords: Hif-1α; bone regeneration; copper nanocomposites; graphene oxides; vascularization.

MeSH terms

  • Animals
  • Bone Cements / chemistry
  • Bone Cements / pharmacology
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / metabolism
  • Bone Morphogenetic Protein 2 / metabolism
  • Bone Regeneration / drug effects*
  • Calcium Phosphates / chemistry
  • Calcium Phosphates / pharmacology*
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Copper / chemistry*
  • Graphite / chemistry*
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Mesenchymal Stem Cells / drug effects
  • Nanocomposites
  • Neovascularization, Physiologic / drug effects*
  • Osteogenesis / physiology
  • Oxides / chemistry*
  • Porosity
  • Rats
  • Rats, Inbred F344
  • Tissue Engineering / methods
  • Tissue Scaffolds

Substances

  • Bone Cements
  • Bone Morphogenetic Protein 2
  • Calcium Phosphates
  • Hif1a protein, rat
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Oxides
  • Graphite
  • Copper
  • calcium phosphate