Rabie A B M, Dai J, Xu R
Biomedical and Tissue Engineering Group, Faculty of Dentistry, The University of Hong Kong, Hong Kong SAR, China.
Gene Ther. 2007 Jun;14(12):972-80. doi: 10.1038/sj.gt.3302943. Epub 2007 Apr 26.
Craniofacial anomalies resulting from impaired growth of mandibular condyles require multidisciplinary interventions, which impose a substantial burden on patients and their families. So far, correcting such deformities with an alternative strategy - gene therapy - is still an uncharted territory. Here, we established an effective in vivo gene delivery system with recombinant adeno-associated virus (rAAV)-mediated vascular endothelial growth factor (VEGF) to enhance mandibular condylar growth. With in situ hybridization, RT-PCR, immunostaining and Western blot, transgene expression was clearly detected in the mandibular condyles during the whole experiment periods. At defined time points, specific osteogenetic markers (alkaline phosphatase and osteocalcin) and chondrogenetic markers (collagen type II and collagen type X) were assessed by means of biochemical analysis and their expression significantly changed from day 30. Proliferation index by proliferating cell nuclear antigen staining showed also a significant increase in cell proliferation. Morphological measurement identified that the size of mandibular condyle significantly increased from day 30. Taken together, rAAV-VEGF was successfully established as an efficient delivery system to induce mandibular condylar growth, which provides the basis for future gene therapy to treat patients with craniofacial deformities.
下颌髁突生长受损导致的颅面畸形需要多学科干预,这给患者及其家庭带来了沉重负担。到目前为止,用一种替代策略——基因治疗来纠正这种畸形仍是一个未知领域。在此,我们建立了一种有效的体内基因递送系统,利用重组腺相关病毒(rAAV)介导血管内皮生长因子(VEGF)来促进下颌髁突生长。通过原位杂交、RT-PCR、免疫染色和蛋白质印迹法,在整个实验期间均能在下颌髁突中清晰检测到转基因表达。在特定时间点,通过生化分析评估了特定的成骨标志物(碱性磷酸酶和骨钙素)和软骨生成标志物(II型胶原蛋白和X型胶原蛋白),其表达从第30天起显著变化。通过增殖细胞核抗原染色得出的增殖指数也显示细胞增殖显著增加。形态学测量表明,下颌髁突的大小从第30天起显著增加。综上所述,rAAV-VEGF成功建立为一种诱导下颌髁突生长的有效递送系统,为未来治疗颅面畸形患者的基因治疗提供了基础。