Tissue engineering‐based cartilage repair with mesenchymal stem cells in a porcine model |
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Authors: | Chih‐Hung Chang Tzong‐Fu Kuo Feng‐Huei Lin Jyh‐Horng Wang Yuan‐Ming Hsu Huei‐Ting Huang Shiao‐Tung Loo Hsu‐Wei Fang Hwa‐Chang Liu Wen‐Chih Wang |
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Affiliation: | 1. Division of Orthopedics, Department of Surgery, Far Eastern Memorial Hospital, Pan‐Chiao 220, New Taipei City, Taiwan, ROC;2. Graduate School of Biotechnology and Bioengineering, Yuan Ze University, Tao‐Yuan, Taiwan, ROC;3. Department of Orthopedic Surgery, National Taiwan University Hospital, Taipei 100, Taiwan, ROC;4. School of Veterinary Medicine, National Taiwan University, Taipei, Taiwan, ROC;5. Institute of Biomedical Engineering, National Taiwan University, Taipei 100, Taiwan, ROC;6. Department of Chemical Engineering & Biotechnology, Institute of Biotechnology, National Taipei University of Technology, Taipei, Taiwan, ROC;7. Division of Medical Engineering Research, National Health Research Institutes, Miaoli County, Taiwan, ROC;8. Department of Orthopedic Surgery, Taiwan Adventist Hospital, Taipei, Taiwan, ROC;9. Department of Orthopedic Surgery, En Chu Kong Hospital, San‐Shia, New Taipei City, Taiwan, ROC |
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Abstract: | ![]() This in vivo pilot study explored the use of mesenchymal stem cell (MSC) containing tissue engineering constructs in repair of osteochondral defects. Osteochondral defects were created in the medial condyles of both knees of 16 miniature pigs. One joint received a cell/collagen tissue engineering construct with or without pretreatment with transforming growth factor β (TGF‐β) and the other joint from the same pig received no treatment or the gel scaffold only. Six months after surgery, in knees with no treatment, all defects showed contracted craters; in those treated with the gel scaffold alone, six showed a smooth gross surface, one a hypertrophic surface, and one a contracted crater; in those with undifferentiated MSCs, five defects had smooth, fully repaired surfaces or partially repaired surfaces, and one defect poor repair; in those with TGF‐β‐induced differentiated MSCs, seven defects had smooth, fully repaired surfaces or partially repaired surfaces, and three defects showed poor repair. In Pineda score grading, the group with undifferentiated MSC, but not the group with TGF‐β‐induced differentiated MSCs, had significantly lower subchondral, cell morphology, and total scores than the groups with no or gel‐only treatment. The compressive stiffness was larger in cartilage without surgical treatment than the treated area within each group. In conclusion, this preliminary pilot study suggests that using undifferentiated MSCs might be a better approach than using TGF‐β‐induced differentiated MSCs for in vivo tissue engineered treatment of osteochondral defects. © 2011 Orthopaedic Research Society Published by Wiley Periodicals, Inc. J Orthop Res 29:1874–1880, 2011 |
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Keywords: | cartilage cartilage tissue engineering in vivo test mesenchymal stem cell transforming growth factor |
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