Enhancing bone regeneration by combining mesenchymal stem cell sheets with β-TCP/COL-I scaffolds

被引:28
作者
Lin, Jun [1 ]
Shao, Jiaqi [1 ]
Juan, Li [1 ]
Yu, Wenke [1 ]
Song, Xiaojia [1 ]
Liu, Pengruofeng [1 ]
Weng, Wenjian [2 ]
Xu, Jinghong [3 ]
Mehl, Christian [4 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 1, Dept Stomatol, Hangzhou 310003, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Mat Sci & Engn, Hangzhou 310027, Peoples R China
[3] Zhejiang Univ, Affiliated Hosp 1, Dept Plast Surg, Hangzhou 310003, Zhejiang, Peoples R China
[4] Christian Albrechts Univ Kiel, Dept Prosthodont Propaedeut & Dent Mat, D-2415 Kiel, Germany
基金
中国国家自然科学基金;
关键词
mesenchymal stem cells; beta-TCP; COL-I scaffold; bone regeneration; ELISA; quantitative real-time polymerase chain reaction; MARROW STROMAL CELLS; TRICALCIUM PHOSPHATE; CALCIUM-PHOSPHATE; TISSUE; TRANSPLANTATION; DEFECTS; MATRIX; VITRO; TCP; MEDICINE;
D O I
10.1002/jbm.b.34003
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The combination of bone marrow-derived mesenchymal stem cells (BMSCs) and biological scaffolds has been demonstrated to be a promising strategy for bone regeneration. However, this method does not result in satisfactory bone regeneration, because the BMSCs are dispersed in the biological scaffolds. The current study developed a new bone regeneration system, which combines synthetic porous three-dimensional scaffolds of -TCP/COL-I composite with cultured osteogenic sheets of BMSCs. Activity of alkaline phosphatase (ALP), a marker of bone regeneration, was assayed in vitro using enzyme-linked immunosorbent assays and quantitative real-time polymerase chain reaction. In vivo bone regeneration was assayed in male nude mice. The study samples were BMSC sheet, scaffold/scattered BMSCs, scaffold/BMSC sheet, and scaffold alone. The samples were implanted dorsally in the mice. In vitro analysis showed that -TCP/COL-I scaffold combined with BMSC sheets significantly upregulated both gene expression and protein levels of ALP, osteocalcin, and osteopontin. Histological and micro-computed tomography showed that the only implants that demonstrated new bone formation after 4 weeks were scaffold/BMSC sheet implants. These results underscore the crucial requirement of a synergistic effect of -TCP/COL-I scaffolds and BMSC sheets. This could be a promising novel strategy for bone tissue engineering. (c) 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 2037-2045, 2018.
引用
收藏
页码:2037 / 2045
页数:9
相关论文
共 56 条
[51]   A Copolymer Scaffold Functionalized with Nanodiamond Particles Enhances Osteogenic Metabolic Activity and Bone Regeneration [J].
Yassin, Mohammed A. ;
Mustafa, Kamal ;
Xing, Zhe ;
Sun, Yang ;
Fasmer, Kristine Eldevik ;
Waag, Thilo ;
Krueger, Anke ;
Steinmueller-Nethl, Doris ;
Finne-Wistrand, Anna ;
Leknes, Knut N. .
MACROMOLECULAR BIOSCIENCE, 2017, 17 (06)
[52]   Osteogenesis of the construct combined BMSCs with β-TCP in rat [J].
Zhang, Mingyu ;
Wang, Kunzheng ;
Shi, Zhibin ;
Yang, Huaqing ;
Dang, Xiaoqian ;
Wang, Wei .
JOURNAL OF PLASTIC RECONSTRUCTIVE AND AESTHETIC SURGERY, 2010, 63 (02) :227-232
[53]   Combination of β-TCP and BMP-2 gene-modified bMSCs to heal critical size mandibular defects in rats [J].
Zhao, J. ;
Hu, J. ;
Wang, S. ;
Sun, X. ;
Xia, L. ;
Zhang, X. ;
Zhang, Z. ;
Jiang, X. .
ORAL DISEASES, 2010, 16 (01) :46-54
[54]   Leptin Overexpression in Bone Marrow Stromal Cells Promotes Periodontal Regeneration in a Rat Model of Osteoporosis [J].
Zheng, Baoyu ;
Jiang, Jun ;
Chen, Yuling ;
Lin, Minkui ;
Du, Zhibin ;
Xiao, Yin ;
Luo, Kai ;
Yan, Fuhua .
JOURNAL OF PERIODONTOLOGY, 2017, 88 (08) :808-818
[55]   Combined marrow stromal cell-sheet techniques and high-strength biodegradable composite scaffolds for engineered functional bone grafts [J].
Zhou, Yefang ;
Chen, Fulin ;
Ho, Saey Tuan ;
Woodruff, Maria Ann ;
Lim, Tit Meng ;
Hutmacher, Dietmar W. .
BIOMATERIALS, 2007, 28 (05) :814-824
[56]   Preparation and characterization of porous β-tricalcium phosphate collagen composites with an integrated structure [J].
Zou, C ;
Weng, WJ ;
Deng, XL ;
Cheng, K ;
Liu, XG ;
Du, PY ;
Shen, G ;
Han, GR .
BIOMATERIALS, 2005, 26 (26) :5276-5284