2014 Volume No 27 – pages 350-364
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Title: Performance of different three-dimensional scaffolds for in vivo endochondral bone generation |
Author: W Yang, SK Both, GJVM van Osch, Y Wang, JA Jansen, F Yang |
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Address: Department of Biomaterials, Radboud University Medical Center, Dentistry 309, P.O. Box 9101, 6500 HB, Nijmegen, The Netherlands
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E-mail: fang.yang at radboudumc.nl |
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Key Words: Bone regeneration, scaffold, mesenchymal stem cells, endochondral bone formation, subcutaneous implantation. |
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Publication date: June 10th 2014 |
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Abstract: In the context of skeletal tissue development and repair, endochondral ossification has inspired a new approach to regenerate bone tissue in vivo using a cartilage intermediate as an osteoinductive template. The aim of this study was to investigate the behavior of mesenchymal stem cells (MSCs) in regard to in vitro cartilage formation and in vivo bone regeneration when combined with different three-dimensional (3D) scaffold materials, i.e., hydroxyapatite/tricalcium phosphate (HA/TCP) composite block, polyurethane (PU) foam, poly(lactic-co-glycolic acid)/poly(ε-caprolactone) electrospun fibers (PLGA/PCL) and collagen I gel. To this end, rat MSCs were seeded on these scaffolds and chondrogenically differentiated in vitro for 4 weeks followed by in vivo subcutaneous implantation for 8 weeks. Nonetheless, the quality and maturity of in vivo ectopic bone formation appeared to be scaffold/material-dependent. Eight weeks of implantation was not sufficient to ossify the entire PLGA/PCL constructs, albeit a comprehensive remodeling of the cartilage had occurred. For HA/TCP, PU and collagen I scaffolds, more mature bone formation with rich vascularity and marrow stroma development could be observed. These data suggest that chondrogenic priming of MSCs in the presence of different scaffold materials allows the establishment of reliable templates for generating functional endochondral bone tissue in vivo without using osteoinductive growth factors. The morphology and maturity of bone formation.
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Article download: Pages
350-364 (PDF file) |
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