Controlled delivery of mesenchymal stem cells and growth factors using a nanofiber scaffold for tendon repair

被引:116
|
作者
Manning, C. N. [1 ]
Schwartz, A. G. [1 ]
Liu, W. [2 ]
Xie, J. [3 ]
Havlioglu, N. [4 ]
Sakiyama-Elbert, S. E. [3 ]
Silva, M. J. [1 ]
Xia, Y. [5 ]
Gelberman, R. H. [1 ]
Thomopoulos, S. [1 ]
机构
[1] Washington Univ, Dept Orthopaed Surg, St Louis, MO USA
[2] Georgia Inst Technol, Dept Chem & Biomol Engn, Atlanta, GA 30332 USA
[3] Washington Univ, Dept Biomed Engn, St Louis, MO USA
[4] St Louis Univ Hosp, Dept Pathol, St Louis, MO USA
[5] Georgia Inst Technol, Dept Biomed Engn, Atlanta, GA 30332 USA
基金
美国国家卫生研究院;
关键词
Sustained delivery system; Electrospinning; Stem cells; Tissue engineering; Intrasynovial flexor tendon; MARROW STROMAL CELLS; VERSUS-HOST-DISEASE; IN-VITRO; FLEXOR TENDONS; REGENERATIVE MEDICINE; OSTEOGENIC DIFFERENTIATION; CONTROLLED-RELEASE; UPPER EXTREMITY; CARDIAC REPAIR; GENE-TRANSFER;
D O I
10.1016/j.actbio.2013.02.008
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Outcomes after tendon repair are often unsatisfactory, despite improvements in surgical techniques and rehabilitation methods. Recent studies aimed at enhancing repair have targeted the paucicellular nature of tendon for enhancing repair; however, most approaches for delivering growth factors and cells have not been designed for dense connective tissues such as tendon. Therefore, we developed a scaffold capable of delivering growth factors and cells in a surgically manageable form for tendon repair. Platelet-derived growth factor BB (PDGF-BB), along with adipose-derived mesenchymal stem cells (ASCs), were incorporated into a heparin/fibrin-based delivery system (HBDS). This hydrogel was then layered with an electrospun nanofiber poly(lactic-co-glycolic acid) (PLGA) backbone. The HBDS allowed for the concurrent delivery of PDGF-BB and ASCs in a controlled manner, while the PLGA backbone provided structural integrity for surgical handling and tendon implantation. In vitro studies verified that the cells remained viable, and that sustained growth factor release was achieved. In vivo studies in a large animal tendon model verified that the approach was clinically relevant, and that the cells remained viable in the tendon repair environment. Only a mild immunoresponse was seen at dissection, histologically, and at the mRNA level; fiuorescently labeled ASCs and the scaffold were found at the repair site 9 days post-operatively; and increased total DNA was observed in ASC-treated tendons. The novel layered scaffold has the potential for improving tendon healing due to its ability to deliver both cells and growth factors simultaneously in a surgically convenient manner. (C) 2013 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:6905 / 6914
页数:10
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