Scaffold degradation elevates the Collagen content and dynamic compressive modulus in engineered articular cartilage

被引:32
作者
Ng, K. W. [1 ]
Kugler, L. E. [1 ]
Doty, S. B. [3 ]
Ateshian, G. A. [2 ]
Hung, C. T. [1 ]
机构
[1] Columbia Univ, Dept Biomed Engn, Cellular Engn Lab, New York, NY 10027 USA
[2] Columbia Univ, Dept Mech Engn, Musculoskeletal Biomech Lab, New York, NY 10027 USA
[3] Hosp Special Surg, Analyt Microscopy Lab, New York, NY 10021 USA
关键词
Cartilage; Tissue engineering; Agarose; Biomaterials; Scaffold; Degradation; Mechanical properties; Agarase; SEEDED ALGINATE CONSTRUCTS; BOVINE NASAL CARTILAGE; AGAROSE GELS; IN-VITRO; MECHANICAL STIMULATION; CONFINED COMPRESSION; CHONDROITIN SULFATE; FINE-STRUCTURE; TISSUE; MATRIX;
D O I
10.1016/j.joca.2008.06.013
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Objective: It was hypothesized that controlled, scaffold removal in engineered cartilage constructs would improve their collagen content and mechanical properties over time in culture. Design: Preliminary experiments characterized the effects of agarase on cell-free agarose disks and cartilage explants. Immature bovine chondrocytes were encapsulated in agarose, cultured to day 42, and incubated with 100 units/mL agarase for 48 h. After treatment, constructs were cultured to day 91. The compressive Young's modulus and dynamic modulus of the constructs were determined every 2 weeks and immediately after agarase treatment. Post-mechanical testing, constructs were processed for biochemistry and histology. Results: Agarase treatment on explants had no detrimental effect on the cartilage matrix. Treatment applied to engineered constructs on day 42 did not affect DNA or collagen content. Agarase treatment decreased tissue GAG content (via GAG loss to the media) and Young's modulus, both of which recovered to control values over time in culture. By day 91 agarase-treated constructs possessed similar to 25% more DNA, similar to 60% more collagen, and similar to 40% higher dynamic modulus compared to untreated controls. Conclusions: Scaffold degradation increased construct collagen content and dynamic mechanical properties, affirming the experimental hypothesis. The mechanism may lie in increased nutrient transport, increased space for collagen fibril formation, and cellular response to the loss of GAG with agarase treatment. The results highlight the role of the scaffold in retaining synthesized matrix during early and late tissue formation. This work also shows promise in developing an engineered tissue that may be completely free of scaffold material for clinical implantation. (C) 2008 Published by Elsevier Ltd on behalf of Osteoarthritis Research Society International.
引用
收藏
页码:220 / 227
页数:8
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