Santos Marina I, Tuzlakoglu Kadriye, Fuchs Sabine, Gomes Manuela E, Peters Kirsten, Unger Ronald E, Piskin Erhan, Reis Rui L, Kirkpatrick C James
3B's Research Group - Biomaterials, Biodegradables and Biomimetics, Department of Polymer Engineering, University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal.
Biomaterials. 2008 Nov;29(32):4306-13. doi: 10.1016/j.biomaterials.2008.07.033. Epub 2008 Aug 15.
Presently the majority of tissue engineering approaches aimed at regenerating bone relies only on post-implantation vascularization. Strategies that include seeding endothelial cells (ECs) on biomaterials and promoting their adhesion, migration and functionality might be a solution for the formation of vascularized bone. Nano/micro-fiber-combined scaffolds have an innovative structure, inspired by extracellular matrix (ECM) that combines a nano-network, aimed to promote cell adhesion, with a micro-fiber mesh that provides the mechanical support. In this work we addressed the influence of this nano-network on growth pattern, morphology, inflammatory expression profile, expression of structural proteins, homotypic interactions and angiogenic potential of human EC cultured on a scaffold made of a blend of starch and poly(caprolactone). The nano-network allowed cells to span between individual micro-fibers and influenced cell morphology. Furthermore, on nano-fibers as well as on micro-fibers ECs maintained the physiological expression pattern of the structural protein vimentin and PECAM-1 between adjacent cells. In addition, ECs growing on the nano/micro-fiber-combined scaffold were sensitive to pro-inflammatory stimulus. Under pro-angiogenic conditions in vitro, the ECM-like nano-network provided the structural and organizational stability for ECs' migration and organization into capillary-like structures. The architecture of nano/micro-fiber-combined scaffolds elicited and guided the 3D distribution of ECs without compromising the structural requirements for bone regeneration.
目前,大多数旨在再生骨的组织工程方法仅依赖植入后的血管化。将内皮细胞(ECs)接种在生物材料上并促进其黏附、迁移和功能的策略可能是形成血管化骨的一种解决方案。纳米/微纤维复合支架具有创新结构,其灵感来源于细胞外基质(ECM),它结合了旨在促进细胞黏附的纳米网络和提供机械支撑的微纤维网。在这项工作中,我们研究了这种纳米网络对在由淀粉和聚己内酯共混物制成的支架上培养的人ECs的生长模式、形态、炎症表达谱、结构蛋白表达、同型相互作用和血管生成潜力的影响。纳米网络使细胞能够跨越单个微纤维并影响细胞形态。此外,在纳米纤维以及微纤维上,ECs维持了相邻细胞间结构蛋白波形蛋白和血小板内皮细胞黏附分子-1(PECAM-1)的生理表达模式。此外,在纳米/微纤维复合支架上生长的ECs对促炎刺激敏感。在体外促血管生成条件下,类似ECM的纳米网络为ECs迁移并组织成毛细血管样结构提供了结构和组织稳定性。纳米/微纤维复合支架的结构引发并引导了ECs的三维分布,同时不影响骨再生的结构要求。