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Induction of angiogenesis in tissue-engineered scaffolds designed for bone repair: A combined gene therapy–cell transplantation approach

机译:设计用于骨修复的组织工程支架中的血管生成诱导:基因治疗-细胞移植的联合方法

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摘要

One of the fundamental principles underlying tissue engineering approaches is that newly formed tissue must maintain sufficient vascularization to support its growth. Efforts to induce vascular growth into tissue-engineered scaffolds have recently been dedicated to developing novel strategies to deliver specific biological factors that direct the recruitment of endothelial cell (EC) progenitors and their differentiation. The challenge, however, lies in orchestration of the cells, appropriate biological factors, and optimal factor doses. This study reports an approach as a step forward to resolving this dilemma by combining an ex vivo gene transfer strategy and EC transplantation. The utility of this approach was evaluated by using 3D poly(lactide-co-glycolide) (PLAGA) sintered microsphere scaffolds for bone tissue engineering applications. Our goal was achieved by isolation and transfection of adipose-derived stromal cells (ADSCs) with adenovirus encoding the cDNA of VEGF. We demonstrated that the combination of VEGF releasing ADSCs and ECs results in marked vascular growth within PLAGA scaffolds. We thereby delineate the potential of ADSCs to promote vascular growth into biomaterials.
机译:组织工程方法的基本原理之一是,新形成的组织必须维持足够的血管形成以支持其生长。最近致力于将血管生长引入组织工程支架的努力致力于开发新颖的策略,以提供特定的生物因子,这些因子指导内皮细胞(EC)祖细胞的募集及其分化。然而,挑战在于细胞的编排,适当的生物学因子和最佳因子剂量。这项研究报告了一种通过结合体外基因转移策略和EC移植来解决这一难题的方法。通过将3D聚丙交酯-乙交酯共聚物(PLAGA)烧结的微球支架用于骨组织工程应用,评估了该方法的实用性。我们的目标是通过用编码VEGF cDNA的腺病毒分离和转染脂肪来源的基质细胞(ADSCs)来实现的。我们证明,VEGF释放的ADSCs和ECs的组合导致PLAGA支架内明显的血管生长。因此,我们描述了ADSCs促进血管生长为生物材料的潜力。

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