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基于生物可还原 PDMAEMA-SS-PEG-SS-PDMAEMA 三嵌段共聚物的可逆屏蔽 DNA 超分子复合物介导显著增强的非病毒基因转染。

Reversibly shielded DNA polyplexes based on bioreducible PDMAEMA-SS-PEG-SS-PDMAEMA triblock copolymers mediate markedly enhanced nonviral gene transfection.

机构信息

Biomedical Polymers Laboratory, and Jiangsu Key Laboratory of Advanced Functional Polymer Design and Application, Department of Polymer Science and Engineering, College of Chemistry, Chemical Engineering and Materials Science, Soochow University , Suzhou, 215123, People's Republic of China.

出版信息

Biomacromolecules. 2012 Mar 12;13(3):769-78. doi: 10.1021/bm201693j. Epub 2012 Feb 10.

Abstract

Reversibly shielded DNA polyplexes based on bioreducible poly(dimethylaminoethyl methacrylate)-SS-poly(ethylene glycol)-SS-poly(dimethylaminoethyl methacrylate) (PDMAEMA-SS-PEG-SS-PDMAEMA) triblock copolymers were designed, prepared and investigated for in vitro gene transfection. Two PDMAEMA-SS-PEG-SS-PDMAEMA copolymers with controlled compositions, 6.6-6-6.6 and 13-6-13 kDa, were obtained by reversible addition-fragmentation chain transfer (RAFT) polymerization of dimethylaminoethyl methacrylate (DMAEMA) using CPADN-SS-PEG-SS-CPADN (CPADN: 4-cyanopentanoic acid dithionaphthalenoate; PEG: 6 kDa) as a macro-RAFT agent. Like their nonreducible PDMAEMA-PEG-PDMAEMA analogues, PDMAEMA-SS-PEG-SS-PDMAEMA triblock copolymers could effectively condense DNA into small particles with average diameters less than 120 nm and close to neutral zeta potentials (0 ∼ +6 mV) at and above an N/P ratio of 3/1. The resulting polyplexes showed excellent colloidal stability against 150 mM NaCl, which contrasts with polyplexes of 20 kDa PDMAEMA homopolymer. In the presence of 10 mM dithiothreitol (DTT), however, polyplexes of PDMAEMA-SS-PEG-SS-PDMAEMA were rapidly deshielded and unpacked, as revealed by significant increase of positive surface charges as well as increase of particle sizes to over 1000 nm. Release of DNA in response to 10 mM DTT was further confirmed by gel retardation assays. These polyplexes, either stably or reversibly shielded, revealed a low cytotoxicity (over 80% cell viability) at and below an N/P ratio of 12/1. Notably, in vitro transfection studies showed that reversibly shielded polyplexes afforded up to 28 times higher transfection efficacy as compared to stably shielded control under otherwise the same conditions. Confocal laser scanning microscope (CLSM) studies revealed that reversibly shielded polyplexes efficiently delivered and released pDNA into the perinuclei region as well as nuclei of COS-7 cells. Hence, reduction-sensitive reversibly shielded DNA polyplexes based on PDMAEMA-SS-PEG-SS-PDMAEMA are highly promising for nonviral gene transfection.

摘要

基于生物可还原的聚(二甲基氨基乙基甲基丙烯酸酯)-SS-聚(乙二醇)-SS-聚(二甲基氨基乙基甲基丙烯酸酯)(PDMAEMA-SS-PEG-SS-PDMAEMA)三嵌段共聚物的可逆屏蔽 DNA 多聚物被设计、制备并用于体外基因转染。两种具有受控组成的 PDMAEMA-SS-PEG-SS-PDMAEMA 共聚物,6.6-6-6.6 和 13-6-13 kDa,通过可逆加成-断裂链转移(RAFT)聚合二甲基氨基乙基甲基丙烯酸酯(DMAEMA)使用 CPADN-SS-PEG-SS-CPADN(CPADN:4-氰基戊酸二硫代萘酸酯;PEG:6 kDa)作为大分子 RAFT 试剂获得。与它们的不可还原 PDMAEMA-PEG-PDMAEMA 类似物一样,PDMAEMA-SS-PEG-SS-PDMAEMA 三嵌段共聚物可以有效地将 DNA 浓缩成平均直径小于 120nm 且接近中性 ζ 电位(0 ∼ +6 mV)的小颗粒,在 N/P 比为 3/1 及以上时。所得的多聚物在 150 mM NaCl 存在下显示出极好的胶体稳定性,这与 20 kDa PDMAEMA 均聚物的多聚物形成鲜明对比。然而,在 10 mM 二硫苏糖醇(DTT)的存在下,PDMAEMA-SS-PEG-SS-PDMAEMA 多聚物迅速去屏蔽和解包,这表现为正表面电荷的显著增加以及颗粒尺寸增加到超过 1000nm。通过凝胶阻滞实验进一步证实了 DNA 的释放响应 10 mM DTT。这些多聚物,无论是稳定屏蔽还是可逆屏蔽,在 N/P 比为 12/1 及以下时显示出低细胞毒性(超过 80%细胞活力)。值得注意的是,体外转染研究表明,在相同条件下,与稳定屏蔽对照相比,可逆屏蔽多聚物的转染效率高达 28 倍。共聚焦激光扫描显微镜(CLSM)研究表明,可逆屏蔽的多聚物能够将 pDNA 有效地递送到 COS-7 细胞的核周区和核内,并释放出来。因此,基于 PDMAEMA-SS-PEG-SS-PDMAEMA 的还原敏感的可逆屏蔽 DNA 多聚物在非病毒基因转染中具有很高的应用前景。

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