In vivo study of anterior cruciate ligament regeneration using mesenchymal stem cells and silk scaffold

被引:194
作者
Fan, Hongbin [1 ]
Liu, Haifeng [1 ]
Wong, Eugene J. W. [1 ]
Toh, Siew L. [1 ,2 ]
Goh, James C. H. [1 ]
机构
[1] Natl Univ Singapore, Dept Orthopaed Surg, Div Bioengn, Singapore 117548, Singapore
[2] Natl Univ Singapore, Dept Mech Engn, Singapore 117548, Singapore
关键词
tissue engineering; ligament; silk; regeneration; mesenchyrnal stem cells;
D O I
10.1016/j.biomaterials.2008.04.012
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Although most in vitro studies indicate that silk is a suitable biomaterial for ligament tissue engineering, in vivo studies of implanted silk scaffolds for ligament reconstruction are still lacking. The objective of this study is to investigate anterior cruciate ligament (ACL) regeneration using mesenchymal stem cells (MSCs) and silk scaffold. The scaffold was fabricated by incorporating microporous silk sponges into knitted silk mesh, which mimicked the structures of ligament extracellular matrix (ECM). In vitro culture demonstrated that MSCs on scaffolds proliferated vigorously and produced abundant collagen. The transcription levels of ligament-specific genes also increased with time. Then MSCs/scaffold was implanted to regenerate ACL in vivo. After 24 weeks, histology observation showed that MSCs were distributed throughout the regenerated ligament and exhibited fibroblast morphology. The key ligament ECM components including collagen I, collagen 111, and tenascin-C were produced prominently. Furthermore, direct ligament-bone insertion with typical four zones (bone, mineralized fibrocartilage, fibrocartilage, ligament) was reconstructed, which resembled the native structure of ACL-bone insertion. The tensile strength of regenerated ligament also met the mechanical requirements. Moreover, its histological grading score was significantly higher than that of control. In conclusion, the results imply that silk scaffold has great potentials in future clinical applications. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3324 / 3337
页数:14
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