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Abstract
This study aimed to study the effects of initial cell density and in vitro culture method on the construction of tissue-engineered bone grafts and osteogenic activities. Human mesenchymal stem cells (hMSCs) were seeded onto cubic scaffolds prepared from demineralized bone matrix (DBM) by three methods - static, hydrodynamic, or fibrin hydrogel-assisted seeding. The resulting cell-scaffold constructs were cultured in vitro by static flask culture or hydrodynamic culture. The initial cell density and the subsequent in vitro proliferation and alkaline phosphate activities of the constructs were analyzed. The constructs were also subcutaneously implanted in nude mice to examine their in vivo osteogenic activities. Hydrogel-assisted seeding gave the highest seeding efficiency, followed by hydrodynamic and conventional static seeding. During in vitro culture, hydrodynamic culture produced higher plateau cell densities, alkaline phosphatase (ALP) activities, and extracellular matrix production than static culture. After subcutaneous implantation in nude mice, the implants prepared by the combination of hydrogel-assisted seeding and hydrodynamic culture produced higher wet weight and bone mineral density than implants prepared by other methods. The results suggest that the hydrogel-assisted seeding can substantially increase the initial seed cell density in scaffolds. Subsequent hydrodynamic culture can promote the proliferation and osteoblastic differentiation of the seeded cells. Correspondingly, bone grafts produced by the combination of these two methods achieved the highest osteogenic activity among the three methods employed.
Highlights
Reconstruction of critical-size bone deficiencies remains a major challenge in orthopedics
This study aims to understand the effects of the key factors of tissue engineering preparation methods, including initial cell density and hydrodynamic culture methods, in an attempt to provide experimental basis for improvement the osteogenesis performance of bone tissue engineering
The Human mesenchymal stem cells (hMSCs) stained immunohistochemically positive for alkaline phosphatase (ALP) (Fig. 1B and C), osteocalcin (Fig. 1E and F) and collagen type I (Fig. 1H and I) after 12-day osteogenic induction
Summary
Reconstruction of critical-size bone deficiencies remains a major challenge in orthopedics. A suspension containing seeded cells is dispensed on a scaffold, followed by a period of rest to allow the cells to enter the scaffold With this method, the initial cell density (the number of cells which attached in 3D scaffold when tissue engineering bone were preparation and without culturing in vivo or in vitro) in the scaffold can be increased by increasing the cell concentration of the suspension within a certain range, though at the expense of seeding efficiency (i.e. the percentage of cells that entered the scaffold), but cannot be further increased beyond a plateau level [6]. Dynamic fluid flow may result in cell detachment and shear-induced damage, and loss in cell utilization [3,12]
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