Histological assessment of bioengineered new bone in repairing osteoperiosteal mandibular defects in sheep using recombinant human bone morphogenetic protein-7
British Journal of Oral and Maxillofacial Surgery, ISSN: 0266-4356, Vol: 42, Issue: 5, Page: 410-418
2004
- 23Citations
- 38Captures
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Metrics Details
- Citations23
- Citation Indexes23
- 23
- CrossRef15
- Captures38
- Readers38
- 38
Article Description
Numerous experimental studies have been published about osteoinductive bone morphogenetic proteins (BMPs). However, to our knowledge there has been no detailed histological study of a mandibular defect in a large mammal, reconstructed using BMPs. We describe here the histological features of rhBMP-7-induced bone in mandibular defects in sheep. Methods : A 35 mm osteoperiosteal defect was created at the parasymphyseal region of the mandible in six adult sheep. The continuity of the mandible was maintained using a bony plate, and rhBMP-7 was applied on a type I collagen carrier. Bone labels were injected at selected time intervals during the follow-up period. The animals were killed after 3 months and bone samples were examined histologically, histomorphometrically, and by fluorescence microscopy. Results and conclusions : We found a mixture of woven and lamellar bone that contained many cells with large nuclei. This had not reorganised to form cortical bone and the rhBMP-7-induced bone was more porous than the native bone. The newly-formed bone restored both endosteal and periosteal layers. rhBMP-7-induced bone was biocompatible and induced no ossification of soft tissue or abnormal growth of nearby vital structures. The mineral apposition rate was 1.98 μm/day (range 0.62–5.63 μm/day), a value close to that reported in humans. This suggests that BMPs have a limited effect in accelerating the rate of mineralisation, but promote the pre-mineralisation processes, and perhaps the formation of woven bone.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S026643560400097X; http://dx.doi.org/10.1016/j.bjoms.2004.05.005; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=4444333492&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/15336766; http://linkinghub.elsevier.com/retrieve/pii/S026643560400097X; http://api.elsevier.com/content/article/PII:S026643560400097X?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:S026643560400097X?httpAccept=text/plain; http://dx.doi.org/10.1016/s0266-4356(04)00097-x; https://linkinghub.elsevier.com/retrieve/pii/S026643560400097X; https://dx.doi.org/10.1016/j.bjoms.2004.05.005
Elsevier BV
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