Cell-Derived Polymer/Extracellular Matrix Composite Scaffolds for Cartilage Regeneration, Part 1: Investigation of Cocultures and Seeding Densities for Improved Extracellular Matrix Deposition

被引:0
作者
Levorson, Erica J. [1 ]
Mountziaris, Paschalia M. [1 ]
Hu, Olivia [1 ]
Kasper, F. Kurtis [1 ]
Mikos, Antonios G. [1 ]
机构
[1] Rice Univ, Dept Bioengn, Houston, TX 77005 USA
基金
美国国家卫生研究院;
关键词
MESENCHYMAL STEM-CELLS; HUMAN ARTICULAR CHONDROCYTES; AUTOLOGOUS BONE-MARROW; CHONDROGENIC DIFFERENTIATION; REPAIR; PROTEIN; HYPERTROPHY; CONSTRUCTS; EXPRESSION; MATURATION;
D O I
10.1089/ten.tec.2013.0286
中图分类号
Q813 [细胞工程];
学科分类号
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(e-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.
引用
收藏
页码:340 / 357
页数:18
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