Xenopus Laevis as a Novel Model to Study Long Bone Critical-Size Defect Repair by Growth Factor-Mediated Regeneration

• Published in: Tissue engineering. Part A 2011-03, Vol.17 (5-6), p.691-701
• Main Authors: Feng, Liang, Milner, Derek J., Xia, Chunguang, Nye, Holly L.D., Redwood, Patrick, Cameron, Jo Ann, Stocum, David L., Fang, Nick, Jasiuk, Iwona
• Format: Article
• Language: English
• Subjects: Animals; Bone and Bones - drug effects; Bone and Bones - pathology; Bone and Bones - surgery; Bone density; Bone Morphogenetic Protein 4 - pharmacology; Bone morphogenetic proteins; Bone Regeneration - drug effects; Growth factors; Humans; Implants, Experimental; Microscopy, Electron, Scanning; Models, Animal; Muscles; Original Articles; Physiological aspects; Porosity - drug effects; Regeneration; Tissue engineering; Tissue Scaffolds - chemistry; Vascular Endothelial Growth Factor A - pharmacology; Wound Healing - drug effects; Xenopus laevis
• ISSN: 1937-3341; 1937-335X
• DOI: 10.1089/ten.tea.2010.0123

We used the tarsus of an adult Xenopus laevis frog as an in vivo load-bearing model to study the regeneration of critical-size defects (CSD) in long bones. We found the CSD for this bone to be about 35% of the tarsus length. To promote regeneration, we implanted biocompatible 1,6 hexanediol diacrylate scaffolds soaked with bone morphogenetic proteins-4 and vascular endothelial growth factors. In contrast to studies that use scaffolds as templates for bone formation, we used scaffolds as a growth factor delivery vehicle to promote cartilage-to-bone regeneration. Defects in control frogs were filled with scaffolds lacking growth factors. The limbs were harvested at a series of time points ranging from 3 weeks to 6 months after implantation and evaluated using micro-computed tomography and histology. In frogs treated with growth factor-loaded scaffolds, we observed a cartilage-to-bone regeneration in the skeletal defect. Five out of eight defects were completely filled with cartilage by 6 weeks. Blood vessels had invaded the cartilage, and bone was beginning to form in ossifying centers. By 3 months, these processes were well advanced, and extensive ossification was observed in 6-month samples. In contrast, the defects in control frogs showed only formation of fibrous scar tissue. This study demonstrates the utility of a Xenopus model system for tissue engineering research and that the normal in vivo mechanism of endochondral bone development and fracture repair can be mimicked in the repair of CSD with scaffolds used as growth factor delivery mechanisms.