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One-Step Fabrication of Bone Morphogenetic Protein-2 Gene-Activated Porous Poly-L-Lactide Scaffold for Bone Induction

机译:一步一步制备骨形态发生蛋白2基因激活的多孔聚L-丙交酯骨诱导支架。

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摘要

Bone morphogenetic protein 2 (BMP2) is an efficacious inducer for the osteogenesis of mesenchymal stem cells (MSCs). Conventional applications of BMP2 have involved either the direct incorporation of BMP2 protein or ex vivo BMP2 gene transfer into stem cells prior to their transplantation. These approaches are able to promote bone formation to some extent; however, they are hampered by either the lack of stability and sustainability of BMP2 protein or the time-consuming and cost-prohibitive in vitro cell culture procedure. To overcome these limitations, we have developed a gene-activated poly-L-lactide acid (PLLA) scaffold with the encapsulation of recombinant adeno-associated viral (AAV) vector encoding a full-length cDNA of human BMP2 using an ice-based microparticle porogenization method that was recently developed. Results showed continuous release of AAV particles from the micropores of scaffolds for up to 1 week, subsequently transducing embedded human MSCs and producing functional BMP2. MSCs within scaffolds underwent efficacious osteogenesis, on the basis of osteoinductive gene expression and osteogenic differentiation, which resulted in robust new bone formation in vivo at 4 weeks. These findings show the potential of the technology toward developing clinical applications of a rapid, cost-effective, and potentially point-of-care approach for the repair of bone defects.
机译:骨形态发生蛋白2(BMP2)是间充质干细胞(MSCs)成骨的有效诱导剂。 BMP2的常规应用涉及将BMP2蛋白直接掺入或将BMP2基因体外移植到干细胞中。这些方法能够在一定程度上促进骨骼的形成。但是,由于缺乏BMP2蛋白的稳定性和可持续性,或者体外细胞培养过程中耗时且成本高昂的问题,它们受到了阻碍。为了克服这些局限性,我们已经开发了一种基因激活的聚L-丙酸(PLLA)支架,并使用基于冰的微粒封装了重组腺相关病毒(AAV)载体,该载体编码人BMP2的全长cDNA最近开发的成孔方法。结果显示AAV颗粒从支架的微孔中连续释放长达1周,随后转导了包埋的人类MSC,并产生了功能性BMP2。根据骨诱导基因表达和成骨分化,支架内的MSC进行了有效的成骨作用,从而在4周内在体内形成了坚固的新骨。这些发现表明,该技术具有潜力,可以开发出一种快速,经济有效且可能具有即时医疗服务的方法来修复骨缺损。

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