BMP-2 gene-fibronectin-apatite composite layer enhances bone formation

J Biomed Sci. 2011 Aug 23;18(1):62. doi: 10.1186/1423-0127-18-62.

Abstract

Background: Safe and efficient gene transfer systems are needed for tissue engineering. We have developed an apatite composite layer including the bone morphogenetic protein-2 (BMP-2) gene and fibronectin (FB), and we evaluated its ability to induce bone formation.

Methods: An apatite composite layer was evaluated to determine the efficiency of gene transfer to cells cultured on it. Cells were cultured on a composite layer including the BMP-2 gene and FB, and BMP-2 gene expression, BMP-2 protein concentrations, alkaline phosphatase (ALP) activity, and osteocalcin (OC) concentrations were measured. A bone defect on the cranium of rats was treated with hydroxyapatite (HAP)-coated ceramic buttons with the apatite composite layer including the BMP-2 gene and FB (HAP-BMP-FB). The tissue concentration of BMP-2, bone formation, and the expression levels of the BMP-2, ALP, and OC genes were all quantified.

Results: The apatite composite layer provided more efficient gene transfer for the cultured cells than an apatite composite layer without FB. The BMP-2 concentration was approximately 100-600 pg/mL in the cell-culture medium. Culturing the cells on the apatite composite layer for 27 days increased ALP activity and OC concentrations. In animal experiments, the tissue concentrations of BMP-2 were over 100 pg/mg in the HAP-BMP-FB group and approximately 50 pg/mg in the control groups. Eight weeks later, bone formation was more enhanced in the HAP-BMP-FB group than in the control groups. In the tissues surrounding the HAP button, the gene expression levels of ALP and OC increased.

Conclusion: The BMP-2 gene-FB-apatite composite layer might be useful for bone engineering.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Alkaline Phosphatase / metabolism
  • Animals
  • Bone Morphogenetic Protein 2 / genetics
  • Bone Morphogenetic Protein 2 / metabolism
  • Bone Morphogenetic Protein 2 / physiology*
  • Calcium Phosphates / metabolism
  • Cells, Cultured
  • DNA Primers / genetics
  • Durapatite / metabolism*
  • Enzyme-Linked Immunosorbent Assay
  • Fibronectins / physiology*
  • Gene Transfer Techniques*
  • HeLa Cells
  • Humans
  • Membrane Proteins / metabolism
  • Mice
  • Microscopy, Electron, Scanning
  • Osteocalcin / metabolism
  • Osteogenesis / genetics
  • Osteogenesis / physiology*
  • Plasmids / genetics
  • Rats
  • Reverse Transcriptase Polymerase Chain Reaction
  • Skull / injuries
  • Skull / surgery
  • Tissue Engineering / methods*

Substances

  • Adaptor Proteins, Signal Transducing
  • Atrnl1 protein, mouse
  • Bone Morphogenetic Protein 2
  • Calcium Phosphates
  • DNA Primers
  • Fibronectins
  • Membrane Proteins
  • Osteocalcin
  • Durapatite
  • calcium phosphate
  • Alkaline Phosphatase