Abstract
Bone matrix (BM) is an acellular crosslinked porcine-derived cancellous bone graft, and therefore may provide advantages over other synthetic and naturally derived materials for use in orthopaedic surgery. Here, we analysed the potential of BM to support the growth and differentiation of primary human multipotent stromal cells/mesenchymal stem cells (MSCs) in order to predict in vivo bone regeneration events. Imaging with laser scanning confocal microscopy and scanning electron microscopy showed that 1 day after static seeding, a dense population of viable MSCs could be achieved on scaffolds suggesting they could be used for in vivo delivery of cells to the implant site. Long-term growth analysis by confocal imaging and histology demonstrated that BM was permissive to the growth and the 3D population of primary MSCs and an enhanced green fluorescent protein expressing osteosarcoma cell line, eGFP.MG63s, over several days in culture. Measurement of alkaline phosphatase (ALP) activities and mRNA expression levels of osteogenic markers (Runx-2, ALP, collagen type I, osteonectin, osteocalcin and osteopontin) indicated that BM supported osteogenesis of MSCs when supplemented with osteogenic stimulants. Upregulation of some of these osteogenic markers on BM, but not on tissue culture plastic, under non-osteogenic conditions suggested that BM also had osteoinductive capacities.
| Original language | English |
|---|---|
| Article number | 025006 |
| Pages (from-to) | 025006 |
| Journal | Biomedical materials (Bristol, England) |
| Volume | 6 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - Apr 2011 |
Keywords
- Animals
- Bone Marrow Cells
- Bone Transplantation
- Bone and Bones
- Cell Differentiation
- Cell Line, Tumor
- Cells, Cultured
- Cross-Linking Reagents
- Green Fluorescent Proteins
- Mesenchymal Stem Cells
- Microscopy, Confocal
- Microscopy, Electron, Scanning
- Orthopedics
- Osteosarcoma
- Swine