Academic Department of Trauma and Orthopaedics, Leeds General Infirmary, Great George Street, Leeds LS1 3EX, UK.
Injury. 2009 Dec;40 Suppl 3:S1-3. doi: 10.1016/S0020-1383(09)00642-1.
Ongoing research at the molecular level has expanded our understanding of the physiological processes that regulate the complex phenomena of fracture healing and bone regeneration. A number of key molecules have been identified and shown to facilitate the progression of healing from one stage to another, leading to an uneventful outcome. Among these candidate molecules, bone morphogenetic proteins (BMPs) possess potent osteoinductive properties. They interact with osteoprogenitor cells, regulating both mitogenesis and differentiation potential. Since the discovery of BMPs, a number of experimental and clinical trials have supported their safety and efficacy of their use in therapy. Nonetheless, at times their efficacy falls short of expectations. Several factors have been identified as contributing to this result. It is anticipated that, as our knowledge expands and we understand better the complex pathways and cascades of molecular events attributable to BMPs, the application of these molecules in the clinical setting will continue to increase and to show more favourable outcomes.
目前在分子水平上的研究已经扩展了我们对调节骨折愈合和骨再生这一复杂现象的生理过程的理解。已经确定了许多关键分子,并表明它们有助于从一个阶段到另一个阶段的愈合进展,从而导致顺利的结果。在这些候选分子中,骨形态发生蛋白(BMPs)具有强大的成骨诱导特性。它们与成骨前体细胞相互作用,调节有丝分裂和分化潜能。自发现 BMPs 以来,许多实验和临床试验都支持了它们的安全性和治疗用途的功效。尽管如此,有时它们的疗效并不如预期的那样。已经确定了几个因素导致了这一结果。随着我们知识的扩展,我们更好地理解了归因于 BMPs 的复杂途径和分子事件级联,预计这些分子在临床环境中的应用将继续增加,并显示出更有利的结果。