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用于软骨再生的细胞衍生聚合物/细胞外基质复合支架,第2部分:构建体失活及软骨诱导能力的测定

Cell-derived polymer/extracellular matrix composite scaffolds for cartilage regeneration, Part 2: construct devitalization and determination of chondroinductive capacity.

作者信息

Levorson Erica J, Hu Olivia, Mountziaris Paschalia M, Kasper F Kurtis, Mikos Antonios G

机构信息

Department of Bioengineering, Rice University , Houston, Texas.

出版信息

Tissue Eng Part C Methods. 2014 Apr;20(4):358-72. doi: 10.1089/ten.tec.2013.0288. Epub 2013 Oct 12.

Abstract

This work examined the chondrogenic potential of chondrocyte and mesenchymal stem cell (MSC) coculture generated poly(ɛ-caprolactone) (PCL)/extracellular matrix (ECM) hybrid scaffolds. Five different ratios of chondrocytes and MSCs were cocultured to generate cartilage-like ECM within electrospun fibrous scaffolds for 7, 14, and 21 days. These constructs were then devitalized to isolate the chondrogenic effects of the ECM alone. Devitalization was successful at removing cellular matter from the scaffolds, yet did reduce the amount of matrix present in the scaffolds. Following devitalization, the PCL/ECM scaffolds were then cultured with MSCs in serum-free conditions with or without TGF-β3 treatment for 21 days. TGF-β3 supplemented culture caused an induction of chondrogenesis in each scaffold type, but also somewhat masked the subtle differences of the different ECM coatings. Without TGF-β3, the cartilaginous matrix generated by 1:1 cocultures of chondrocytes to MSCs for 14 days supported similar chondrogenic gene expression patterns of MSCs cultured on scaffolds generated by chondrocytes alone. These scaffold formulations had a positive chondrogenic effect on aggrecan, collagen type II, and collagen II/I expression when compared to PCL controls. This study demonstrates that it is possible to utilize cocultures of chondrocytes and MSCs to coat a polymer scaffold with cartilage-like ECM capable of supporting chondrogenic differentiation of MSCs.

摘要

这项研究考察了软骨细胞与间充质干细胞(MSC)共培养生成的聚己内酯(PCL)/细胞外基质(ECM)混合支架的软骨生成潜力。将软骨细胞与MSC按五种不同比例共培养,在静电纺丝纤维支架内生成类软骨ECM,培养7天、14天和21天。然后使这些构建体失活,以单独分离ECM的软骨生成作用。失活成功去除了支架中的细胞物质,但确实减少了支架中存在的基质数量。失活后,将PCL/ECM支架在无血清条件下与MSC一起培养,添加或不添加转化生长因子-β3(TGF-β3),培养21天。添加TGF-β3的培养诱导了每种支架类型的软骨生成,但也在一定程度上掩盖了不同ECM涂层的细微差异。在不添加TGF-β3的情况下,软骨细胞与MSC按1:1共培养14天生成的软骨基质支持的MSC软骨生成基因表达模式,与单独由软骨细胞生成的支架上培养的MSC相似。与PCL对照相比,这些支架配方对聚集蛋白聚糖、II型胶原蛋白和胶原蛋白II/I的表达具有积极的软骨生成作用。这项研究表明,利用软骨细胞与MSC共培养,用能够支持MSC软骨生成分化的类软骨ECM包被聚合物支架是可行的。

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