Department of Mining and Materials Engineering, McGill University, Montreal, H3A 0C1, Canada.
Faculty of Dentistry, Department of Medicine, and Shriners Hospital for Children, McGill University, Montreal, Quebec, H4A 0A9, Canada.
Adv Healthc Mater. 2023 Oct;12(25):e2300211. doi: 10.1002/adhm.202300211. Epub 2023 Jul 27.
Bone tissue engineering using stem cells to build bone directly on a scaffold matrix often fails due to lack of oxygen at the injury site. This may be avoided by following the endochondral ossification route; herein, a cartilage template is promoted first, which can survive hypoxic environments, followed by its hypertrophy and ossification. However, hypertrophy is so far only achieved using biological factors. This work introduces a Bioglass-Poly(lactic-co-glycolic acid@fibrin (Bg-PLGA@fibrin) construct where a fibrin hydrogel infiltrates and encapsulates a porous Bg-PLGA. The hypothesis is that mesenchymal stem cells (MSCs) loaded in the fibrin gel and induced into chondrogenesis degrade the gel and become hypertrophic upon reaching the stiffer, bioactive Bg-PLGA core, without external induction factors. Results show that Bg-PLGA@fibrin induces hypertrophy, as well as matrix mineralization and osteogenesis; it also promotes a change in morphology of the MSCs at the gel/scaffold interface, possibly a sign of osteoblast-like differentiation of hypertrophic chondrocytes. Thus, the Bg-PLGA@fibrin construct can sequentially support the different phases of endochondral ossification purely based on material cues. This may facilitate clinical translation by decreasing in-vitro cell culture time pre-implantation and the complexity associated with the use of external induction factors.
使用干细胞在支架基质上直接构建骨组织的骨组织工程经常由于损伤部位缺氧而失败。通过遵循软骨内成骨途径可以避免这种情况;在此过程中,首先促进软骨模板的形成,软骨模板可以在低氧环境中存活,然后发生肥大和骨化。然而,迄今为止,肥大仅通过生物因子来实现。本工作介绍了一种 Bioglass-Poly(lactic-co-glycolic acid@fibrin (Bg-PLGA@fibrin) 构建体,其中纤维蛋白凝胶渗透并包裹多孔的 Bg-PLGA。假设是将负载在纤维蛋白凝胶中的间充质干细胞 (MSCs) 诱导为软骨细胞,当它们到达更硬的、生物活性的 Bg-PLGA 核心时,在没有外部诱导因子的情况下,凝胶会降解并发生肥大。结果表明,Bg-PLGA@fibrin 诱导了肥大、基质矿化和成骨;它还促进了凝胶/支架界面处 MSCs 形态的变化,可能是肥大软骨细胞向成骨细胞样分化的标志。因此,基于材料线索,Bg-PLGA@fibrin 构建体可以依次支持软骨内成骨的不同阶段。这可能通过减少植入前体外细胞培养时间和与使用外部诱导因子相关的复杂性来促进临床转化。