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首页> 外文期刊>Tissue engineering, Part C. Methods >Cell-derived polymer/extracellular matrix composite scaffolds for cartilage regeneration, part 1: Investigation of cocultures and seeding densities for improved extracellular matrix deposition
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Cell-derived polymer/extracellular matrix composite scaffolds for cartilage regeneration, part 1: Investigation of cocultures and seeding densities for improved extracellular matrix deposition

机译:用于软骨再生的细胞来源的聚合物/细胞外基质复合支架,第1部分:共培养和接种密度研究以改善细胞外基质沉积

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摘要

This study investigated the coculture of chondrocytes and mesenchymal stem cells (MSCs) on electrospun fibrous polymer scaffolds to produce polymer/extracellular matrix (ECM) hybrid constructs with the objective of reducing the number of chondrocytes necessary to produce ample cartilage-like ECM within the scaffolds. To generate these hybrid constructs, electrospun poly(ε-caprolactone) fibrous scaffolds were seeded at both high and low initial densities with five different ratios of chondrocytes to MSCs: 1:0, 1:1, 1:3, 1:5, and 0:1, and cultured for 7, 14, and 21 days. Glycosaminoglycan production and distribution within the three coculture groups was similar to quantities generated by chondrocyte-only controls. Conversely, as the concentration of chondrocytes was increased, the collagen content of the constructs also increased at each time point, with a 1:1 chondrocyte to MSC ratio approximating the collagen production of chondrocytes alone. Histological staining suggested that cocultured constructs mimicked the well-distributed ECM patterns of chondrocyte generated constructs, while improving greatly over the restricted distribution of matrix within MSC-only constructs. These results support the capacity of cocultures of chondrocytes and MSCs to generate cartilaginous matrix within a polymeric scaffold. Further, the inclusion of MSCs in these cocultures enables the reduction of chondrocytes needed to produce cell-generated ECM.
机译:这项研究调查了在静电纺丝纤维聚合物支架上共培养软骨细胞和间充质干细胞(MSC)以生产聚合物/细胞外基质(ECM)杂合构建体的目的,目的是减少在支架中产生足够的软骨样ECM所需的软骨细胞数量。 。为了生成这些杂合构建体,将静电纺丝的聚(ε-己内酯)纤维支架分别以高和低初始密度接种,其中软骨细胞与MSC的比率为5:1、0、1:1、1:3、1:5和5。 0:1,并培养7、14和21天。糖胺聚糖在三个共培养组中的产生和分布与仅软骨细胞的对照组产生的数量相似。相反,随着软骨细胞浓度的增加,构建体的胶原蛋白含量也在每个时间点增加,软骨细胞与MSC的比例为1:1,近似于单独软骨细胞的胶原蛋白产量。组织学染色表明,共培养的构建体模仿软骨细胞生成的构建体的良好分布的ECM模式,同时大大改善了仅MSC构建体中基质的受限分布。这些结果支持了软骨细胞和MSC的共培养在聚合物支架内产生软骨基质的能力。此外,在这些共培养物中包含MSC能够减少产生细胞产生的ECM所需的软骨细胞。

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