Bacterial cellulose-hydroxyapatite composites with osteogenic growth peptide (OGP) or pentapeptide OGP on bone regeneration in critical-size calvarial defect model

J Biomed Mater Res A. 2015 Oct;103(10):3397-406. doi: 10.1002/jbm.a.35472. Epub 2015 Jul 7.

Abstract

This study aimed to evaluate the potential of bacterial cellulose-hydroxyapatite (BC-HA) composites associated with osteogenic growth peptide (OGP) or pentapeptide OGP(10-14) in bone regeneration in critical-size calvarial defects in mice. In this study, the BC-HA, BC-HA-OGP, and BC-HA-OGP(10-14) membranes were analyzed at 3, 7, 15, 30, 60, and 90 days. In each period, the specimens were evaluated by micro-computed tomography (µCT), descriptive histology, gene expression of bone biomarkers by qPCR and VEGFR-2 (vascular endothelial growth factor) quantification by ELISA. Three days post-operative, Runx2, Tnfrsf11b and Bglap bone biomarkers were upregulated mainly by BC-HA OGP and BC-HA OGP(10-14) membranes, suggesting an acceleration of the osteoblast differentiation/activity with the use of these biomaterials. At 60 and 90 days, a high percentage of bone formation was observed by µCT for BC-HA and BC-HA OGP(10-14) membranes. High expression of some bone biomarkers, such as Alpl, Spp1, and Tnfrsf11b, was also observed for the same membranes on days 60 and 90. In conclusion, the BC-HA membrane promoted a better bone formation in critical-size mice calvarial defects. Nevertheless, incorporation of the peptides at the concentration of 10(-9) mol L(-1) did not improve bone regeneration potential in the long-term.

Keywords: bacterial cellulose; biomaterial; bone regeneration; gene expression; osteogenic peptide.

MeSH terms

  • Animals
  • Antigens, Differentiation / metabolism
  • Bacteria / chemistry*
  • Bone Regeneration / drug effects*
  • Bone Substitutes* / chemistry
  • Bone Substitutes* / pharmacology
  • Cellulose* / chemistry
  • Cellulose* / pharmacology
  • Disease Models, Animal
  • Durapatite* / chemistry
  • Durapatite* / pharmacology
  • Histones* / chemistry
  • Histones* / pharmacology
  • Intercellular Signaling Peptides and Proteins* / chemistry
  • Intercellular Signaling Peptides and Proteins* / pharmacology
  • Male
  • Materials Testing
  • Mice
  • Mice, Inbred BALB C
  • Skull / injuries*
  • Skull / metabolism
  • Skull / pathology

Substances

  • Antigens, Differentiation
  • Bone Substitutes
  • Histones
  • Intercellular Signaling Peptides and Proteins
  • osteogenic growth peptide
  • Cellulose
  • Durapatite