Franceschi Renny T, Yang Shuying, Rutherford R Bruce, Krebsbach Paul H, Zhao Ming, Wang Dian
The Center for Craniofacial Regeneration, University of Michigan School of Dentistry, Ann Arbor, Mich., USA.
Cells Tissues Organs. 2004;176(1-3):95-108. doi: 10.1159/000075031.
Gene therapy represents a promising approach for delivering regenerative molecules to specific tissues including bone. Several laboratories have shown that virus-based BMP expression vectors can stimulate osteoblast differentiation and bone formation in vivo. Both in vivo and ex vivo transduction of cells can induce bone formation at ectopic and orthotopic sites. Adenovirus and direct DNA delivery of genes encoding regenerative molecules can heal critical-sized defects of cranial and long bones. Although osteogenic activity can be demonstrated for individual BMP vectors, substantial synergies may be achieved using combinatorial gene therapy to express complimentary osteogenic signals including specific combinations of BMPs or BMPs and transcription factors. Further control of the bone regeneration process may also be achieved through the use of inducible promoters that can be used to control the timing and magnitude of expression for a particular gene. Using these types of approaches, it should be possible to mimic natural processes of bone development and fracture repair and, in so doing, be able to precisely control both the amount and type of bone regenerated.
基因治疗是一种将再生分子递送至包括骨骼在内的特定组织的有前景的方法。多个实验室已表明,基于病毒的骨形态发生蛋白(BMP)表达载体可在体内刺激成骨细胞分化和骨形成。细胞的体内和体外转导均可在异位和原位诱导骨形成。腺病毒以及编码再生分子的基因的直接DNA递送可治愈颅骨和长骨的临界尺寸缺损。尽管单个BMP载体可表现出成骨活性,但使用组合基因疗法来表达包括特定BMP组合或BMP与转录因子的互补成骨信号,可能会实现显著的协同作用。通过使用可诱导启动子,也可进一步控制骨再生过程,该启动子可用于控制特定基因表达的时间和幅度。使用这些类型的方法,应该有可能模拟骨发育和骨折修复的自然过程,并且这样做能够精确控制再生骨的数量和类型。