Shanghai Key Laboratory of Regulatory Biology, School of Life Sciences, East China Normal University , Shanghai, 200241, P. R. China.
Biomacromolecules. 2017 Aug 14;18(8):2371-2378. doi: 10.1021/acs.biomac.7b00567. Epub 2017 Jul 17.
Gene therapy has received considerable attention due to its great potential in the treatment of various diseases; however, the design of efficient and biocompatible carriers for the delivery of siRNA as well as DNA still remains a major challenge. In this study, we developed an efficient carrier for gene delivery by modification of a compound containing both guanidyl and phenyl groups on the surface of a cationic dendrimer. The guanidyl group on the dendrimer facilitates nucleic acid condensation via specific guanidinium-phosphate interactions, whereas the phenyl group on the polymer is critical for efficient endosomal escape. The combination of guanidyl and phenyl shows a synergistic effect in facilitated endocytosis. The designed material is much more efficient in siRNA and DNA delivery than control materials such as dendrimers engineered with a guanidyl or phenyl group only, as well as intact dendrimers, and shows comparable efficacy to commercial transfection reagent Lipofectamine 2000. In addition, the material and its complex with nucleic acid show minimal toxicity on the transfected cells. This study provides a new strategy to develop multifunctional polymers for efficient siRNA and DNA delivery.
基因治疗因其在治疗各种疾病方面的巨大潜力而受到广泛关注;然而,设计高效且生物相容的载体来递送 siRNA 和 DNA 仍然是一个主要挑战。在这项研究中,我们通过修饰一种在阳离子树状大分子表面同时含有胍基和苯基的化合物,开发了一种有效的基因传递载体。树状大分子上的胍基通过特定的胍基-磷酸相互作用促进核酸的凝聚,而聚合物上的苯基对于有效的内体逃逸至关重要。胍基和苯基的组合在促进细胞内吞方面具有协同作用。与仅含有胍基或苯基的树枝状大分子以及完整的树枝状大分子等对照材料相比,设计的材料在 siRNA 和 DNA 传递方面的效率要高得多,与商业转染试剂 Lipofectamine 2000 的效果相当。此外,该材料及其与核酸的复合物在转染细胞上表现出最小的毒性。这项研究为开发用于高效 siRNA 和 DNA 传递的多功能聚合物提供了一种新策略。