Development of a bone reconstruction technique using a solid free-form fabrication (SFF)-based drug releasing scaffold and adipose-derived stem cells

被引:18
|
作者
Lee, Jin Woo [1 ]
Kim, Ki-Joo [2 ]
Kang, Kyung Shin [3 ]
Chen, Shaochen [1 ,4 ]
Rhie, Jong-Won [2 ]
Cho, Dong-Woo [3 ,5 ]
机构
[1] Univ Calif San Diego, Dept NanoEngn, La Jolla, CA 92093 USA
[2] Catholic Univ Korea, Dept Plast Surg, Sch Med, Seoul 137701, South Korea
[3] Pohang Univ Sci & Technol POSTECH, Dept Mech Engn, Pohang 790784, Gyungbuk, South Korea
[4] Univ Calif San Diego, Inst Engn Med, La Jolla, CA 92093 USA
[5] Pohang Univ Sci & Technol POSTECH, Div Integrat Biosci & Biotechnol, Pohang 790784, Gyungbuk, South Korea
基金
新加坡国家研究基金会;
关键词
bone-tissue engineering; scaffold; bone morphogenetic protein (BMP); human adipose-derived stem cells (hADSCs); solid free-form fabrication (SFF); GROWTH-FACTOR; GENE-EXPRESSION; CANINE MODEL; IN-VITRO; TISSUE; DIFFERENTIATION; REGENERATION; BMP-2; MICROSTEREOLITHOGRAPHY; POLYMER;
D O I
10.1002/jbm.a.34485
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
For tissue regeneration, three essential components of scaffolds, signals (biomolecules), and cells are required. Moreover, because bony defects are three-dimensional in many clinical circumstances, an exact 3D scaffold is important. Therefore, we proposed an effective reconstruction tool for cranial defects using human adipose-derived stem cells (hADSCs) and a 3D functional scaffold fabricated by solid free-form fabrication (SFF) technology that secretes biomolecules. We fabricated poly(propylene fumarate)-based 3D scaffolds with embedded microsphere-deliverable bone morphogenetic protein-2 (BMP-2) by microstereolithography. BMP-2-loaded SFF scaffolds with/without hADSCs (SFF/BMP/hADSCs scaffolds and SFF/BMP scaffolds, respectively) and BMP-2-unloaded SFF scaffolds (SFF scaffolds) were then implanted in rat crania, and in vivo bone formation was observed. Analyses of bone formation areas using micro-computed tomography (micro-CT) showed the superiority of SFF/BMP/hADSCs scaffolds. Hematoxylin and eosin stain, Masson's trichrome stain, and collagen type-I stain supported the results of the micro-CT scan. And human leukocyte antigen-ABC showed that seeded, differentiated hADSCs were well grown and changed to the bone tissue at the inside of the scaffold. Results showed that our combination of a functional 3D scaffold and hADSCs may be a useful tool for improving the reconstruction quality of severe bony defects in which thick bone is required. (c) 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2013.
引用
收藏
页码:1865 / 1875
页数:11
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