Scaffold-Free Cartilage Tissue Engineering With a Small Population of Human Nasoseptal Chondrocytes

被引:11
作者
Chiu, Loraine L. Y. [1 ,2 ]
To, William T. H. [3 ]
Lee, John M. [2 ,3 ]
Waldman, Stephen D. [1 ,2 ]
机构
[1] Ryerson Univ, Dept Chem Engn, Toronto, ON, Canada
[2] St Michaels Hosp, Li Ka Shing Knowledge Inst, Toronto, ON, Canada
[3] Univ Toronto, St Michaels Hosp, Dept Otolaryngol Head & Neck Surg, Toronto, ON M5S 1A1, Canada
基金
加拿大健康研究院;
关键词
Cartilage tissue engineering; human nasoseptal cartilage; primary cells; growth factors; scaffold-free; continuous flow bioreactor; NASAL SEPTAL CHONDROCYTES; ARTICULAR CHONDROCYTES; GROWTH-FACTORS; HUMAN SERUM; REDIFFERENTIATION; CONSTRUCTS; RECONSTRUCTION; PROLIFERATION; CULTURE; IMPLANTATION;
D O I
10.1002/lary.26396
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective: Cartilage tissue engineering is a promising approach to provide suitable materials for nasal reconstruction; however, it typically requires large numbers of cells. We have previously shown that a small number of chondrocytes cultivated within a continuous flow bioreactor can elicit substantial tissue growth, but translation to human chondrocytes is not trivial. Here, we aimed to demonstrate the application of the bioreactor to generate large-sized tissues from a small population of primary human nasoseptal chondrocytes. Study Design: Experimental study. Methods: Chondrocytes were cultured in the bioreactor using different medium compositions, with varying amounts of serum and with or without growth factors. Resulting engineered tissues were analyzed for physical properties, biochemical composition, tissue microstructure, and protein localization. Results: Bioreactor-cultivated constructs grown with serum and growth factors (basic fibroblast growth factor and transforming growth factor beta 2) had greater thickness, as well as DNA and glycosaminoglycan (GAG) contents, compared to low serum and no growth factor controls. These constructs also showed the most intense proteoglycan and collagen II staining. Conclusion: The combination of bioreactor conditions, serum, and growth factors allowed the generation of large, thick scaffold-free human cartilaginous tissues that resembled the native nasoseptal cartilage. There also may be implications for patient selection in future clinical applications of these engineered tissues because their GAG content decreased with donor age.
引用
收藏
页码:E91 / E99
页数:9
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