Zellin G
Department of Oral Biochemistry, Faculty of Dentistry, Göteborg University, Sweden.
Swed Dent J Suppl. 1998;129:7-65.
Insufficient or absence of bone healing is a frequent problem within all surgical fields. This often necessitates treatment by autogenous bone grafting. Recently, two new techniques to promote bone healing were introduced, the osteopromotive membrane technique, and local delivery of growth-stimulatory factors, both with a high rate of success in preclinical experiments. The aims of the present series of investigations were to further develop the membrane barrier technique, both by itself as well as in combination with local delivery of growth factors, in animal experiments. During membrane-promoted bone formation, the membrane porosity was found to be of importance for the initial rate of bone formation as well as for the performance of the material in the tissue. In contrast, the final amount of bone was not affected. In a well-known bone healing model, the 5 mm in diameter 'critical size defect' at the rat mandibular ramus, the efficacy of rhBMP-2, rhTGF-beta 1 and rhFGF-2 to promote bone regeneration alone and in combination with barrier membranes was evaluated. Under both conditions, rhBMP-2 was found to be an efficient promoter of bone healing. rhFGF-2 had some stimulatory effect both with and without barrier membranes, whereas rhTGF-beta 1 was found to have a minor stimulatory effect by itself, but in combination with barrier membranes it was inhibitory. These observations were interpreted as being the result of an effect of the growth factors at different levels of the osteoblastic lineage; rhBMP-2 being an inducer of osteoblastic cells from stem cells, whereas rhTGF-beta 1 may primarily act on already committed cells. In contrast, rhFGF-2 may have stimulatory effect at different levels of the lineage. Based on the positive results obtained by the combination of rhBMP-2 and barrier membranes in the rat mandible, this combination was then applied to (i) rabbit radius defects; and (ii) a rat calvarial osteoneogenesis model. In the long bone model, membranes by themselves were insufficient to promote bone healing, but the combination resulted in complete regeneration. In the osteoneogenesis model, the combination of barrier membranes and rhBMP-2 resulted in a 100% increase in the final amount of achievable bone. In the last study, rhFGF-2 (no barrier membranes) was shown to enhance revitalization of autoclaved autogenous bone grafts, a procedure clinically used in craniofacial reconstruction mainly after tumor surgery. The combined use of rhBMP-2 and barrier membranes has great potential to be a useful treatment for improving bone healing and might be an alternative to bone grafting.
骨愈合不足或不愈合是所有外科领域常见的问题。这通常需要采用自体骨移植治疗。最近,引入了两种促进骨愈合的新技术,即骨促进膜技术和生长刺激因子的局部递送,两者在临床前实验中成功率都很高。本系列研究的目的是在动物实验中进一步开发膜屏障技术,包括单独使用以及与生长因子局部递送相结合的方式。在膜促进骨形成过程中,发现膜的孔隙率对骨形成的初始速率以及材料在组织中的性能很重要。相比之下,最终的骨量不受影响。在一个著名的骨愈合模型中,即大鼠下颌支直径5毫米的“临界尺寸缺损”模型中,评估了重组人骨形态发生蛋白-2(rhBMP-2)、重组人转化生长因子-β1(rhTGF-β1)和重组人成纤维细胞生长因子-2(rhFGF-2)单独以及与屏障膜联合促进骨再生的效果。在两种情况下,都发现rhBMP-2是骨愈合的有效促进剂。rhFGF-2无论有无屏障膜都有一定的刺激作用,而rhTGF-β1单独作用时刺激作用较小,但与屏障膜联合时则具有抑制作用。这些观察结果被解释为生长因子在成骨细胞谱系不同水平上作用的结果;rhBMP-2是干细胞分化为成骨细胞的诱导剂,而rhTGF-β1可能主要作用于已分化的细胞。相比之下,rhFGF-2可能在谱系的不同水平上具有刺激作用。基于rhBMP-2与屏障膜联合在大鼠下颌骨实验中获得的阳性结果,该联合方法随后被应用于:(i)兔桡骨缺损;以及(ii)大鼠颅骨骨生成模型。在长骨模型中,单独的膜不足以促进骨愈合,但联合使用则可实现完全再生。在骨生成模型中,屏障膜与rhBMP-2联合使用使最终可获得的骨量增加了100%。在最后一项研究中,rhFGF-2(无屏障膜)被证明可增强经高压灭菌的自体骨移植的活力,这一方法主要用于颅面重建手术,尤其是肿瘤手术后的临床治疗。rhBMP-2与屏障膜的联合使用在改善骨愈合方面具有很大的潜力,可能成为骨移植的替代方法。