目的:探讨血小板源性生长因子B(PDGF-B)基因转染修饰大鼠骨髓闻克质干细胞(MSC)的可行性。方法:应用FAM标记重组真核表达载体系统(pcDNA3-PDGF-B)。以脂质体法转染原代MSC。观察转染结果、表达情况孕对靶细胞活力的影响。结果:MSC的基因转染成功,持续表达时间超过了8周,没有发现明显的细胞毒作用及对细胞活力的显著影响。结论:采用真柱转染技术可以介导外源基因转染MSC,MSC是一种理想的基因载体细胞。可用于PDGF-B的基因治疗。
Objective: To study the feasibility of transfecting platelet-derived growth factoroB (PDGF-B) gene to bone marrow mesenehymal stem cells (MSCs). Methods: Recombinant eukaryofic expression carrier system ( pcDNA3-PDGF-B) was marked with carboxyfluorescein (FAM). Original MSCs were transfected by using liposome technique. The results of transfection and the activity of the target cell were determined. Results: Bone marrow MSCs were successfully transfected with pcDNA3-PDGF-B. The expression of exogenous gene continued over 8 weeks. No cell toxicity and obvious influence on cell activity was found. Conclusion: MSCs can be efficiently transfected with exogenous gene by using eukaryotic transfection technique. MSCs are ideal cells for cell-mediated transfection and can be used in PDGF-B gene therapy.