National Engineering Research Center for Biomaterials , Sichuan University , No. 29, Wangjiang Road , Chengdu 610065 , Sichuan , People's Republic of China.
School of Pharmacy, Faculty of Science and Engineering , University of Wolverhampton , Wulfruna Street , Wolverhampton WV1 1LY , United Kingdom.
Biomacromolecules. 2018 Jun 11;19(6):2214-2226. doi: 10.1021/acs.biomac.8b00273. Epub 2018 Apr 30.
In the progress of designing a gene carrier system, what is urgently needed is a balance of excellent safety and satisfactory efficiency. Herein, a straightforward and versatile synthesis of a cationic guanidine-decorated dendronized pullulan (OGG3P) for efficient genetic photodynamic therapy was proposed. OGG3P was able to block the mobility of DNA from a weight ratio of 2. However, G3P lacking guanidine residues could not block DNA migration until at a weight ratio of 15, revealing guanidination could facilitate DNA condensation via specific guanidinium-phosphate interactions. A zeta potential plateau (∼+23 mV) of OGG3P complexes indicated the nonionic hydrophilic hydroxyl groups in pullulan might neutralize the excessive detrimental cationic charges. There was no obvious cytotoxicity and hemolysis, but also enhancement of transfection efficiency with regard to OGG3P in comparison with that of native G3P in Hela and HEK293T cells. More importantly, we found that the uptake efficiency in Hela cells between OGG3P and G3P complexes was not markedly different. However, guanidination caused changes in uptake pathway and led to macropinocytosis pathway, which may be a crucial reason for improved transfection efficiency. After introducing a therapeutic pKillerRed-mem plasmid, OGG3P complexes achieved significantly enhanced KillerRed protein expression and ROS production under irradiation. ROS-induced cancer cells proliferation suppression was also confirmed. This study highlights the guanidine-decorated dendronized pullulan could emerge as a reliable nonviral gene carrier to specifically deliver therapeutic genes.
在设计基因载体系统的过程中,迫切需要平衡卓越的安全性和令人满意的效率。在此,提出了一种简单而通用的阳离子胍基修饰的支化普鲁兰(OGG3P)的合成方法,用于高效的遗传光动力治疗。OGG3P 能够从重量比为 2 的比例阻止 DNA 的迁移。然而,缺乏胍基残基的 G3P 直到重量比为 15 时才能够阻止 DNA 迁移,这表明胍基化能够通过特异性胍基-磷酸相互作用促进 DNA 凝聚。OGG3P 复合物的 ζ 电位平台(约+23 mV)表明普鲁兰中非离子亲水性的羟基可能中和过多的有害阳离子电荷。与天然 G3P 相比,OGG3P 在 Hela 和 HEK293T 细胞中没有明显的细胞毒性和溶血作用,但转染效率也得到了提高。更重要的是,我们发现 Hela 细胞中 OGG3P 和 G3P 复合物的摄取效率没有明显差异。然而,胍基化导致摄取途径发生变化,导致巨胞饮途径,这可能是转染效率提高的一个关键原因。引入治疗性 pKillerRed-mem 质粒后,OGG3P 复合物在照射下实现了显著增强的 KillerRed 蛋白表达和 ROS 产生。ROS 诱导的癌细胞增殖抑制也得到了证实。本研究强调了胍基修饰的支化普鲁兰可以作为一种可靠的非病毒基因载体,用于特异性递送治疗基因。