Tissue engineering of cartilage using poly-ε-caprolactone nanofiber scaffolds seeded in vivo with periosteal cells

被引:40
作者
Casper, M. E. [1 ]
Fitzsimmons, J. S. [1 ]
Stone, J. J. [1 ]
Meza, A. O. [1 ]
Huang, Y. [1 ]
Ruesink, T. J. [1 ]
O'Driscoll, S. W. [1 ]
Reinholz, G. G. [1 ]
机构
[1] Mayo Clin, Cartilage & Connect Tissue Res Lab, Coll Med, Dept Orthoped Surg, Rochester, MN 55905 USA
关键词
Cartilage; Chondrogenesis; Nanofibers; Periosteum; Transforming growth factor-beta; Poly-epsilon-caprolactone; CONTINUOUS PASSIVE MOTION; MESENCHYMAL STEM-CELLS; FULL-THICKNESS DEFECTS; ARTICULAR-CARTILAGE; JOINT SURFACES; GROWTH-FACTOR; II COLLAGEN; BONE; CHONDROGENESIS; GRAFTS;
D O I
10.1016/j.joca.2010.04.009
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
100224 [整形外科学];
摘要
Objective: To determine the potential of periosteal cells to infiltrate poly-E-caprolactone (PCL) nanofiber scaffolds in vivo and subsequently produce cartilage in vitro. Design: PCL nanofiber scaffolds, with or without chitosan-coating were implanted under periosteum in 6-month-old rabbits. Transforming growth factor-beta 1 (TGF-beta 1) or vehicle was injected into each implant site. After 1, 3, 5 or 7 clays, scaffolds were removed, separated from the periosteum, and the scaffolds and periosteum were cultured separately for 6 weeks under chondrogenic conditions. Sulfated glycosaminoglycan (GAG), type II collagen, DNA content, cartilage yield, and calcium deposition were then analyzed. Results: Cell infiltration was observed in all scaffolds. Cartilage formation in the uncoated scaffolds increased with duration of implantation (maximum at 7 days). Cells in the uncoated scaffolds implanted for 7 days produced significantly higher levels of both GAG 1560 (95% confidence interval (CI), 107-1013) vs 228 (95% CI, 177-278) mu gGAG/mu g DNA] and cartilage yield [9% (95% CI, 3-14%) vs 0.02% (95% CI, 0-0.22%)[compared to chitosan-coated scaffolds (P = 0.006 or less). There was no significant difference in GAG content or cartilage yield between the TGF-beta 1-injected and vehicle-injected scaffolds. However, significantly more mineral deposition was detected in TGF-beta 1-injected scaffolds compared to vehicle-injected scaffolds (P < 0.0001). Cartilage yield from the periosteum, moreover, was significantly increased by subperiosteal TGF-beta 1 injections (P < 0.001). However, this response was reduced when chitosan-coated scaffolds were implanted. Conclusions: This study demonstrates that it is possible to seed PCL nanofiber scaffolds with periosteal cells in vivo and subsequently produce engineered cartilage in vitro. (C) 2010 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:981 / 991
页数:11
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