Zhang Bingyang, Zhang Hu, Dai Sheng, Bi Jingxiu
School of Chemical Engineering University of Adelaide Adelaide Australia.
Eng Life Sci. 2016 Oct 4;17(2):193-203. doi: 10.1002/elsc.201600069. eCollection 2017 Feb.
Highly efficient gene delivery vehicles are pursued to progress gene therapy. In this study, we developed the cell-penetrating peptide-labelled and degradable gene carriers for efficient external gene transfection. The cationic carriers were prepared by coupling low-molecular-weight polyethylenimine (PEI800) with 4'4-dithiodibutyric acid (DA), and HIV-1 Trans-Activator of Transcription (TAT) was conjugated to the carriers as a penetrating peptide. The resulted PEI-DA-TAT was able to condense plasmid DNA (pDNA) into a complex with a hydrodynamic size of around 150 nm under a neutral condition. PEI-DA-TAT showed negligible cytotoxicity to both Hela and HEK 293 cells with the cell viability of more than 80% beyond the carrier concentration of 50 μg/mL. This new carrier displayed better performance in regard to DNA transfection efficiency in comparison with the carriers of non-TAT labelled PEI-DA, commercial PEI25K and low-molecular-weight PEI (PEI800). The transfection efficiency of PEI-DA-TAT was increased by 8% compared with PEI-DA and PEI25K. The experimental findings suggested that the developed PEI-DA-TAT is a promising carrier for efficient DNA delivery with low cytotoxicity for gene therapy.
为推动基因治疗的发展,人们一直在寻求高效的基因传递载体。在本研究中,我们开发了用于高效外源基因转染的细胞穿透肽标记且可降解的基因载体。通过将低分子量聚乙烯亚胺(PEI800)与4,4'-二硫代二丁酸(DA)偶联制备阳离子载体,并将HIV-1转录反式激活因子(TAT)作为穿透肽与载体偶联。所得的PEI-DA-TAT能够在中性条件下将质粒DNA(pDNA)浓缩成流体动力学尺寸约为150 nm的复合物。当载体浓度超过50 μg/mL时,PEI-DA-TAT对Hela和HEK 293细胞均显示出可忽略不计的细胞毒性,细胞活力超过80%。与未标记TAT的PEI-DA载体、市售PEI25K和低分子量聚乙烯亚胺(PEI800)相比,这种新型载体在DNA转染效率方面表现出更好的性能。与PEI-DA和PEI25K相比,PEI-DA-TAT的转染效率提高了8%。实验结果表明,所开发的PEI-DA-TAT是一种有前景的载体,可用于高效DNA传递,且对基因治疗具有低细胞毒性。