Wu Guo-Ping, He Xiao-Chuan, Hu Chun-Bing, Li De-Ping, Yang Zhi-Hui, Guo Li
Department of Plastic and Burns Surgery, The Affiliated Hospital of Luzhou Medical College, Luzhou, Sichuan, People's Republic of China.
Ann Plast Surg. 2012 Sep;69(3):316-25. doi: 10.1097/SAP.0b013e3182119275.
Distraction osteogenesis requires a long consolidation period and has a low but real failure rate. Bone morphogenetic proteins (BMPs) accelerate bone deposition in fractures and critical-sized bone defects. Vascular endothelial growth factor (VEGF) is a promising reagent for inducing angiogenesis, and is an essential coordinator of extracellular matrix remodeling, angiogenesis, and bone formation in the growth plate. However, their effects on mandibular distraction osteogenesis are unknown. We investigated the effect of local delivery of plasmid pIRES-hBMP-2-hVEGF165 into a distraction area by electroporation-mediated approach.A New Zealand rabbit model were used. Activation of the device was commenced after 3 days of latency period and proceeded at the rate of 0.8 mm per day for 7 days. After the completion of activation, the rabbits were randomly divided into 5 groups: group A: recombinant plasmid 2 μg (0.1 μg/μL) pIRES-hVEGF165-hBMP2 was injected into the distraction area after the completion of activation; group B: recombinant plasmid pIRES-hBMP2 was injected into the distraction area; group C: recombinant plasmid pIRES-hVEGF165 was injected into the distraction area; group D: pIRES was injected into the distraction area, and group E: normal saline was injected into the distraction area. After injection every group used electroporation. Subsequently, the rabbits were examined by quantitative computed tomography, mechanical testing, and histomorphometric analysis.BMD of newly formed bone of the distraction area in groups A, B, and C were remarkably higher than those of groups D and E at different times (P < 0.001). At 4 and 8 weeks of consolidation, the crushing strength of 3 points of the newly formed bone in group A was remarkably higher than those of groups B, C, D, and E (P < 0.01). The results demonstrated statistically remarkable increase in regenerated bone in the gene-transfected groups.Electroporation-mediated transfecting recombinant plasmid pIRES-hVEGF165-hBMP2 could produce a satisfactory proceeding of osteogenesis and calcification, which surpassed that of the control group. This finding indicates that a combination of VEGF and BMP may make osteogenesis and angiogenesis appear at the same time. Furthermore, it may magnify the effect of single growth factor, and promote growth and reparative process of bone.
牵张成骨需要较长的巩固期,且失败率虽低但确有发生。骨形态发生蛋白(BMPs)可加速骨折部位和临界尺寸骨缺损处的骨沉积。血管内皮生长因子(VEGF)是一种很有前景的诱导血管生成的试剂,是生长板中细胞外基质重塑、血管生成和骨形成的重要协调因子。然而,它们对下颌骨牵张成骨的影响尚不清楚。我们通过电穿孔介导的方法研究了将质粒pIRES-hBMP-2-hVEGF165局部递送至牵张区域的效果。使用新西兰兔模型。在潜伏期3天后开始启动装置,以每天0.8毫米的速度进行7天。激活完成后,将兔子随机分为5组:A组:激活完成后将2微克(0.1微克/微升)重组质粒pIRES-hVEGF165-hBMP2注入牵张区域;B组:将重组质粒pIRES-hBMP2注入牵张区域;C组:将重组质粒pIRES-hVEGF165注入牵张区域;D组:将pIRES注入牵张区域,E组:将生理盐水注入牵张区域。每组注射后进行电穿孔。随后,对兔子进行定量计算机断层扫描、力学测试和组织形态计量分析。在不同时间,A、B和C组牵张区域新形成骨的骨密度显著高于D组和E组(P<0.001)。在巩固4周和8周时,A组新形成骨三点处的抗压强度显著高于B、C、D和E组(P<0.01)。结果表明基因转染组再生骨有统计学上的显著增加。电穿孔介导转染重组质粒pIRES-hVEGF165-hBMP2可产生令人满意的成骨和钙化过程,超过对照组。这一发现表明VEGF和BMP联合使用可能使成骨和血管生成同时出现。此外,它可能放大单一生长因子的作用,并促进骨的生长和修复过程。