VesselEffects of Initial Cell and Hydrodynamic Culturebioreactor can substantially improve the seeding efficiency and subsequent proliferation and osteoblastic differentiation. We further determined if these improvements translated into enhanced osteogenic activity in a nude mice subcutaneous implantation model. 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.Materials and Methods Ethics buy Peptide M statementNude mice (6 weeks old) were purchased from the Laboratory Animal Center of our university. The animal experiment was approved by the ethics committee of Third Military Medical University and conducted in conformity with the `Guiding Principles for Research Involving Animals and Human Beings’ as adopted by The American Physiological Society.Isolation and characterization of hMSCsHuman mesenchymal stem cells (hMSCs) derived from bone marrow of the iliac crests of young healthy volunteers were provided from Tissue Engineering Research and Development Center of The Third Military Medical University. hMSCs were isolated by density gradient centrifugation in Percoll (density = 1.077 g/mL; Sigma, USA) and adherent culture. The cells were expanded by in vitro 26001275 culture and confirmed to be hMSCs by a previously published method [14]. To induce osteogenic differentiation, the hMSCs were cultured in DMEM/F12 medium supplemented with 10 FBS, 0.1 mM dexamethasone, 10 mM glycerophophate, and 50 mM ascorbic acid [15,16]. After 12 days, the 50-14-6 site induced cells were detected by immunochemistry using antibodies (1:100) for ALP, osteocalcin and collagen type I (Sigma, USA) according to product instructions [17]. At the 12th day after osteoinduction, the ALP activity of induced hMSCs was measured and the osteocalcin concentration in the culture medium of induced hMSCs was detected by an enzyme-linked immunosorbent assay (ELISA) kit (BioSino, Beijing, China).prepared by mixing fibrinogen and thrombin within 90 min under sterile condition. The hMSCs were mixed with a fibrin glue to form a suspension containing 26107 cells/ml. The suspension was added dropwise onto the DBM scaffolds (0.05 ml/scaffold). Then 0.05 ml of catalytic agent was sprayed on each scaffold, and was allowed to stand for 5 min for the glue to gelate. Then the scaffolds were added into the high-aspect ratio vessel of a rotary cell culture system, and were cultured with the same condition of group A. Static seeding and static culture (group C, control group): The hMSCs were dissociated in DMEM/F12 medium into a suspension containing 26107 cells/ml and added dropwise onto the DBM scaffolds (0.05 ml/scaffold). The seeded scaffolds were statically cultured in 24-well plates without additional medium for 2 h, then turned over to reduce the downward flow of liquid and the cell loss, and cultured in the same conditions for another 2 h. Then, each well was filled with 1 ml DMEM/F12 and incubated in an atmosphere of 5 CO2 and 100 relative humidity at 37uC, with a change of medium every 48 h. Hydrogel-assisted seeding and static culture (group D): DMB scaffolds were seeded by the same hydrogel-assisted method as in the group B and were cultured statically in 24-well plates (Corning 3524, USA) containing DME/F12 medium (1 ml/well) and incubated in an atmosphere of 5 CO2 and 100.VesselEffects of Initial Cell and Hydrodynamic Culturebioreactor can substantially improve the seeding efficiency and subsequent proliferation and osteoblastic differentiation. We further determined if these improvements translated into enhanced osteogenic activity in a nude mice subcutaneous implantation model. 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.Materials and Methods Ethics statementNude mice (6 weeks old) were purchased from the Laboratory Animal Center of our university. The animal experiment was approved by the ethics committee of Third Military Medical University and conducted in conformity with the `Guiding Principles for Research Involving Animals and Human Beings’ as adopted by The American Physiological Society.Isolation and characterization of hMSCsHuman mesenchymal stem cells (hMSCs) derived from bone marrow of the iliac crests of young healthy volunteers were provided from Tissue Engineering Research and Development Center of The Third Military Medical University. hMSCs were isolated by density gradient centrifugation in Percoll (density = 1.077 g/mL; Sigma, USA) and adherent culture. The cells were expanded by in vitro 26001275 culture and confirmed to be hMSCs by a previously published method [14]. To induce osteogenic differentiation, the hMSCs were cultured in DMEM/F12 medium supplemented with 10 FBS, 0.1 mM dexamethasone, 10 mM glycerophophate, and 50 mM ascorbic acid [15,16]. After 12 days, the induced cells were detected by immunochemistry using antibodies (1:100) for ALP, osteocalcin and collagen type I (Sigma, USA) according to product instructions [17]. At the 12th day after osteoinduction, the ALP activity of induced hMSCs was measured and the osteocalcin concentration in the culture medium of induced hMSCs was detected by an enzyme-linked immunosorbent assay (ELISA) kit (BioSino, Beijing, China).prepared by mixing fibrinogen and thrombin within 90 min under sterile condition. The hMSCs were mixed with a fibrin glue to form a suspension containing 26107 cells/ml. The suspension was added dropwise onto the DBM scaffolds (0.05 ml/scaffold). Then 0.05 ml of catalytic agent was sprayed on each scaffold, and was allowed to stand for 5 min for the glue to gelate. Then the scaffolds were added into the high-aspect ratio vessel of a rotary cell culture system, and were cultured with the same condition of group A. Static seeding and static culture (group C, control group): The hMSCs were dissociated in DMEM/F12 medium into a suspension containing 26107 cells/ml and added dropwise onto the DBM scaffolds (0.05 ml/scaffold). The seeded scaffolds were statically cultured in 24-well plates without additional medium for 2 h, then turned over to reduce the downward flow of liquid and the cell loss, and cultured in the same conditions for another 2 h. Then, each well was filled with 1 ml DMEM/F12 and incubated in an atmosphere of 5 CO2 and 100 relative humidity at 37uC, with a change of medium every 48 h. Hydrogel-assisted seeding and static culture (group D): DMB scaffolds were seeded by the same hydrogel-assisted method as in the group B and were cultured statically in 24-well plates (Corning 3524, USA) containing DME/F12 medium (1 ml/well) and incubated in an atmosphere of 5 CO2 and 100.
