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dc.contributor.authorPrendergast, Patricken
dc.contributor.authorCHECA ESTEBAN, SARAen
dc.date.accessioned2010-09-16T15:53:47Z
dc.date.available2010-09-16T15:53:47Z
dc.date.issued2010en
dc.date.submitted2010en
dc.identifier.citationSandino, C, Checa, S, Prendergast, PJ, Lacroix, D, Simulation of angiogenesis and cell differentiation in a CaP scaffold subjected to compressive strains using a lattice modeling approach, Biomaterials, 31, 8, 2010, 2446 - 2452en
dc.identifier.otherYen
dc.descriptionPUBLISHEDen
dc.description.abstractMechanical stimuli are one of the factors that influence tissue differentiation. In the development of biomaterials for bone tissue engineering, mechanical stimuli and formation of a vascular network that transport oxygen to cells within the pores of the scaffolds are essential. Angiogenesis and cell differentiation have been simulated in scaffolds of regular porosity; however, the dynamics of differentiation can be different when the porosity is not uniform. The objective of this study was to investigate the effect of the mechanical stimuli and the capillary network formation on cell differentiation within a scaffold of irregular morphology. A porous scaffold of calcium phosphate based glass was used. The pores and the solid phase were discretized using micro computed tomography images. Cell activity was simulated within the interconnected pore domain of the scaffold using a lattice modeling approach. Compressive strains of 0.5 and 1% of total deformation were applied and two cases of mesenchymal stem cells initialization (in vitro seeding and in vivo) were simulated. Similar capillary networks were formed independently of the cell initialization mode and the magnitude of the mechanical strain applied. Most of vessels grew in the pores at the periphery of the scaffolds and were blocked by the walls of the scaffold. When 0.5% of strain was applied, 70% of the pore volume was affected by mechano-regulatory stimuli corresponding to bone formation; however, because of the lack of oxygen, only 40% of the volume was filled with osteoblasts. 40% of volume was filled with chondrocytes and 3% with fibroblasts. When the mechanical strain was increased to 1%, 11% of the pore volume was filled with osteoblasts, 59% with chondrocytes, and 8% with fibroblasts. This study has shown the dynamics of the correlation between mechanical load, angiogenesis and tissue differentiation within a scaffold with irregular morphology.en
dc.description.sponsorshipThe authors acknowledge funding from the Government of Catalonia, the European Commission through the SmartCaP project (NMP3-CT2005-013912) and Science Foundation Ireland. Hanifeh Khayyeri is acknowledged for her help in the discussion of the results.en
dc.format.extent2446en
dc.format.extent2452en
dc.language.isoenen
dc.relation.ispartofseriesBiomaterialsen
dc.relation.ispartofseries31en
dc.relation.ispartofseries8en
dc.rightsYen
dc.subjectBioengineeringen
dc.subjectTissue engineeringen
dc.titleSimulation of angiogenesis and cell differentiation in a CaP scaffold subjected to compressive strains using a lattice modeling approachen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/pprenderen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/checaessen
dc.identifier.rssinternalid62698en
dc.subject.TCDThemeNext Generation Medical Devicesen
dc.identifier.rssurihttp://dx.doi.org/10.1016/j.biomaterials.2009.11.063en
dc.contributor.sponsorScience Foundation Ireland (SFI)en
dc.identifier.urihttp://hdl.handle.net/2262/40660


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