Zheng Qixin, Guo Xiaodong, Duan Deyu, Liu Yong, Wu Yongchao
Department of Orthopaedics, Union Hospital, Tongji Medical College, Huazhong University of Science & Technology, Wuhan 430022.
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2003 Sep;20(3):443-6.
To investigate the effect of basic fibroblast growth factor(bFGF) gene transfection on the proliferation and differentiation of mesenchymal stem cells (MSCs) and to provide basis for accelerating bone defect repairing using gene-enhanced tissue engineering technology, Rabbit periosteum-derived MSCs were transfected with the full-length rat bFGF cDNA in vitro. The transient and stable gene expression of bFGF were determined by immunohistochemistry. The proliferation and the synthesis alkaline phosphatase (ALP) and osteocalcin(OC) of the transfected MSCs were also examined. The results showed that bFGF cDNA could be transferred into osteoblasts and expressed stably at least 4 weeks. The proliferation and OC content of genetically modified MSCs were increased significantly, whereas the ALP activity remained no change. In conclusion, transfer of gene encoding bFGF to MSCs increases its proliferation and osteogenesis property. Based on the successful conjunction of the existing techniques of tissue engineering with the novel possibilities offered by modern gene transfer technology, an innovative concept, molecular tissue engineering, was put forward for the first time. As a new branch of tissue engineering, it represents both a new area and an important trend in tissue engineering research.
为研究碱性成纤维细胞生长因子(bFGF)基因转染对间充质干细胞(MSCs)增殖和分化的影响,为利用基因增强组织工程技术加速骨缺损修复提供依据,体外将大鼠bFGF全长cDNA转染兔骨膜来源的MSCs。采用免疫组织化学法检测bFGF的瞬时和稳定基因表达。同时检测转染后MSCs的增殖以及碱性磷酸酶(ALP)和骨钙素(OC)的合成。结果显示,bFGF cDNA能够转入成骨细胞并至少稳定表达4周。基因修饰的MSCs增殖能力及OC含量显著增加,而ALP活性无变化。综上所述,将编码bFGF的基因转入MSCs可增强其增殖和成骨能力。基于现有组织工程技术与现代基因转移技术新可能的成功结合,首次提出了一个创新概念——分子组织工程。作为组织工程的一个新分支,它代表了组织工程研究的一个新领域和重要趋势。