IRCCS Multimedica, Milan, Italy.
Gene Ther. 2012 Jun;19(6):642-8. doi: 10.1038/gt.2012.19. Epub 2012 Mar 1.
Engineered recombinant viral vectors are a powerful tool for vehiculating genetic information into mammalian cells. Because of their ability to infect both dividing and non-dividing cells with high efficiency, lentiviral vectors have gained particular interest for basic research and preclinical studies in the cardiovascular field. We review here the major applications for lentiviral-vector technology in the cardiovascular field: we will discuss their use in trailing gene expression during the induction of differentiation, in protocols for the isolation of cardiac cells and in the tracking of cardiac cells after transplantation in vivo; we will also describe lentivirally-mediated gene delivery uses, such as the induction of a phenotype of interest in a target cell or the treatment of cardiovascular diseases. In addition, a section of the review will be dedicated to reprogramming approaches, focusing attention on the generation of pluripotent stem cells and on transdifferentiation, two emerging strategies for the production of cardiac myocytes from human cells and for the investigation of human diseases. Finally, in order to give a perspective on their future clinical use we will critically discuss advantages and disadvantages of lentivirus-based strategies for the treatment of cardiovascular diseases.
工程重组病毒载体是将遗传信息递送入哺乳动物细胞的有力工具。由于其能够高效感染分裂和非分裂细胞,慢病毒载体在心血管领域的基础研究和临床前研究中引起了特别的关注。我们在这里综述了慢病毒载体技术在心血管领域的主要应用:我们将讨论它们在诱导分化过程中跟踪基因表达、心肌细胞分离方案以及体内移植后心肌细胞追踪中的应用;我们还将描述慢病毒介导的基因传递用途,如在靶细胞中诱导感兴趣的表型或治疗心血管疾病。此外,本综述的一部分将专门讨论重编程方法,重点关注多能干细胞的产生和转分化,这是从人类细胞产生心肌细胞和研究人类疾病的两种新兴策略。最后,为了展望它们未来的临床应用,我们将批判性地讨论基于慢病毒的策略在治疗心血管疾病方面的优缺点。