scholarly journals In Vitro Localization of Bone Growth Factors in Constructs of Biodegradable Scaffolds Seeded with Marrow Stromal Cells and Cultured in a Flow Perfusion Bioreactor

2006 ◽  
Vol 0 (0) ◽  
pp. 060130063000001
Author(s):  
Manuela E. Gomes ◽  
Carla M. Bossano ◽  
Carol M. Johnston ◽  
Rui L. Reis ◽  
Antonios G. Mikos
2006 ◽  
Vol 19 (03) ◽  
pp. 133-141 ◽  
Author(s):  
H. van Bree ◽  
M. Tshamala

SummaryThe osteogenic potential of red bone marrow was first reported more than 100 years ago. Since then, studies have reported controversial results that do not confirm nor disprove the capacity of fresh red bone marrow to produce bone. Researches have been focused on techniques that improve the efficiency of the bone marrow, including: the increase of the concentration of the mesenchymal stem cells in the aspirated bone marrow, the combination with a ‘carrier’ that helps to maintain the mesenchymal stem cells and guides and supports the vascular ingrowth in the defect, or the combination with bone growth factors that stimulate the marrow stromal cells to differentiate into bone forming cells. Each of these techniques has its drawbacks and increases the expenses of an operation. On the other hand, the synergistic effect observed with these combinations does not resolve the problem of the osteogenic capacity of pure bone marrow, which still remains questionable.


2009 ◽  
Vol 2009 ◽  
pp. 1-7 ◽  
Author(s):  
Alexander M. Sailon ◽  
Alexander C. Allori ◽  
Edward H. Davidson ◽  
Derek D. Reformat ◽  
Robert J. Allen ◽  
...  

Background. Bone engineering requires thicker three-dimensional constructs than the maximum thickness supported by standard cell-culture techniques (2 mm). A flow-perfusion bioreactor was developed to provide chemotransportation to thick (6 mm) scaffolds.Methods. Polyurethane scaffolds, seeded with murine preosteoblasts, were loaded into a novel bioreactor. Control scaffolds remained in static culture. Samples were harvested at days 2, 4, 6, and 8 and analyzed for cellular distribution, viability, metabolic activity, and density at the periphery and core.Results. By day 8, static scaffolds had a periphery cell density of , while in the core it was . Flow-perfused scaffolds demonstrated peripheral cell density of and core density of at day 8.Conclusions. Flow perfusion provides chemotransportation to thick scaffolds. This system may permit high throughput study of 3D tissues in vitro and enable prefabrication of biological constructs large enough to solve clinical problems.


Author(s):  
Maria Elena Lombardo ◽  
Francesco Carfì Pavia ◽  
Emanuela Fabiola Craparo ◽  
Elisa Capuana ◽  
Gennara Cavallaro ◽  
...  

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