Application of induced pluripotent stem (iPS) cells in periodontal tissue regeneration |
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Authors: | Xuejing Duan Qisheng Tu Jin Zhang Jinhai Ye Cesar Sommer Gustavo Mostoslavsky David Kaplan Pishan Yang Jake Chen |
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Affiliation: | 1. Division of Oral Biology, Tufts University School of Dental Medicine, Boston, Massachusetts;2. School of Stomatology, Shandong University, Jinan, Shandong Province, China;3. Institute of Stomatology, School of Stomatology, Nanjing Medical University, Nanjing, Jiangsu Province, China;4. Section of Gastroenterology, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts;5. Department of Biomedical Engineering, Tufts University, Medford, Massachusetts |
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Abstract: | Tissue engineering provides a new paradigm for periodontal tissue regeneration in which proper stem cells and effective cellular factors are very important. The objective of this study was, for the first time, to investigate the capabilities and advantages of periodontal tissue regeneration using induced pluripotent stem (iPS) cells and enamel matrix derivatives (EMD). In this study the effect of EMD gel on iPS cells in vitro was first determined, and then tissue engineering technique was performed to repair periodontal defects in three groups: silk scaffold only; silk scaffold + EMD; and silk scaffold + EMD + iPS cells. EMD greatly enhanced the mRNA expression of Runx2 but inhibited the mRNA expression of OC and mineralization nodule formation in vitro. Transplantation of iPS cells showed higher expression levels of OC, Osx, and Runx2 genes, both 12 and 24 days postsurgery. At 24 days postsurgery in the iPS cell group, histological analysis showed much more new alveolar bone and cementum formation with regenerated periodontal ligament between them. The results showed the commitment role that EMD contributes in mesenchymal progenitors to early cells in the osteogenic lineage. iPS cells combined with EMD provide a valuable tool for periodontal tissue engineering, by promoting the formation of new cementum, alveolar bone, and normal periodontal ligament. J. Cell. Physiol. 226: 150–157, 2010. © 2010 Wiley‐Liss, Inc. |
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