Assessment of stem cell viability in the initial healing period in rabbits with a cranial bone defect according to the type and form of scaffold
Increased bone regeneration has been achieved through the use of stem cells in combination with graft material. However, the survival of transplanted stem cells remains a major concern. The purpose of this study was to evaluate the viability of transplanted mesenchymal stem cells (MSCs) at an early...
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Veröffentlicht in: | Journal of periodontal & implant science 2019, 49(4), , pp.258-267 |
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Sprache: | eng |
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Zusammenfassung: | Increased bone regeneration has been achieved through the use of stem cells in combination with graft material. However, the survival of transplanted stem cells remains a major concern. The purpose of this study was to evaluate the viability of transplanted mesenchymal stem cells (MSCs) at an early time point (24 hours) based on the type and form of the scaffold used, including type I collagen membrane and synthetic bone.
The stem cells were obtained from the periosteum of the otherwise healthy dental patients. Four symmetrical circular defects measuring 6 mm in diameter were made in New Zealand white rabbits using a trephine drill. The defects were grafted with 1) synthetic bone (β-tricalcium phosphate/hydroxyapatite [β-TCP/HA]) and 1×10
MSCs, 2) collagen membrane and 1×10
MSCs, 3) β-TCP/HA+collagen membrane and 1×10
MSCs, or 4) β-TCP/HA, a chipped collagen membrane and 1×10
MSCs. Cellular viability and the cell migration rate were analyzed.
Cells were easily separated from the collagen membrane, but not from synthetic bone. The number of stem cells attached to synthetic bone in groups 1, 3, and 4 seemed to be similar. Cellular viability in group 2 was significantly higher than in the other groups (
0.05).
This study showed that stem cells can be applied when a membrane is used as a scaffold under no or minimal pressure. When space maintenance is needed, stem cells can be loaded onto synthetic bone with a chipped membrane to enhance the survival rate. |
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ISSN: | 2093-2278 2093-2286 |
DOI: | 10.5051/jpis.2019.49.4.258 |