首页> 美国卫生研究院文献>Tissue Engineering. Part C Methods >Cell-Derived Polymer/Extracellular Matrix Composite Scaffolds for Cartilage Regeneration Part 2: Construct Devitalization and Determination of Chondroinductive Capacity
【2h】

Cell-Derived Polymer/Extracellular Matrix Composite Scaffolds for Cartilage Regeneration Part 2: Construct Devitalization and Determination of Chondroinductive Capacity

机译: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:构建物活化和软骨诱导能力的测定

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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.
机译:这项工作检查了软骨细胞和间充质干细胞(MSC)共培养生成的聚(ε-己内酯)(PCL)/细胞外基质(ECM)混合支架的软骨形成潜力。将五种不同比例的软骨细胞和MSC共培养7天,14天和21天,以在电纺纤维支架中生成软骨样ECM。然后使这些构建物失活以分离单独的ECM的软骨形成作用。失活作用成功地从支架中去除了细胞物质,但确实减少了支架中存在的基质数量。失活后,将PCL / ECM支架与MSC在无血清条件下培养,并进行或不进行TGF-β3处理21天。补充TGF-β3的培养物可诱导每种支架类型的软骨形成,但也一定程度上掩盖了不同ECM涂层的细微差别。没有TGF-β3,软骨细胞与MSC 1:1共培养14天产生的软骨基质支持了在单独由软骨细胞产生的支架上培养的MSC的相似软骨形成基因表达模式。与PCL对照相比,这些支架制剂对软骨聚集蛋白聚糖,II型胶原和II / I型胶原的表达具有积极的成软骨作用。这项研究表明,有可能利用软骨细胞和MSC的共培养物,用能够支持MSC软骨分化的软骨样ECM覆盖聚合物支架。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号