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Modified pectin-based carrier for gene delivery: Cellular barriers in gene delivery course

机译:修饰的基于果胶的基因传递载体:基因传递过程中的细胞壁垒

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The use of polysaccharides as DNA carriers has high potential for gene therapy applications. Pectin is a structural plant polysaccharide heterogeneous with respect to its chemical structure. It contains branches rich in galactose residues which serve as potential ligands for membrane receptors interaction. In order to make the anionic pectin applicable for DNA complexation, it was modified with three different amine groups (cationic). Pectin-NH2 was prepared by modifying the galacturonic acids carboxyl groups with primary amine groups and further modified to generate pectin-T (T=N+ H(CH3)(2)) and pectin-NH2-Q (Q=N+(CH3)(3)). All three modified pectins formed complexes with plasmid DNA as indicated by gel electrophoresis analysis. The size and morphology of pectin-NH2/DNA complexes were examined by transmission electron microscopy (TEM). Transfection experiments were carried out with human embryonic kidney cell lines (HEK293). using plasmid DNA encoding for green fluorescence protein (GFP). Transfection efficiency was analyzed by flow cytometry analysis, using FACS. Pectin-NH2-Q was the most efficient carrier. Addition of chloroquine ("tysosomotropic" agent) to transfection medium substantially enhanced the HEK293 transfection, indicating that endocytosis is the preferable internalization pathway and implies on the complex inability to escape the endosome. Pectin's galactose residues contribution to transfection was examined by inhibiting pectin binding to membrane receptors (galectins), using galactose and lactose as competitive inhibitors to this interaction. Resulting reduction of transfection efficiency demonstrated the importance of pectin's galactose residues to HEK293 transfection. Suggesting the modified pectin is a promising non-viral carrier for targeted gene delivery to cancer cells with galactose-binding lectins on their surface. (C) 2008 Elsevier B.V. All rights reserved.
机译:多糖作为DNA载体的用途在基因治疗中具有很高的潜力。果胶是就其化学结构而言是异质的结构植物多糖。它包含富含半乳糖残基的分支,这些残基充当膜受体相互作用的潜在配体。为了使阴离子果胶适用于DNA络合,对它进行了三种不同的胺基(阳离子)修饰。通过用伯胺基修饰半乳糖醛酸羧基制备果胶-NH2,然后进一步修饰以生成果胶-T(T = N + H(CH3)(2))和果胶-NH2-Q(Q = N +(CH3)( 3))。如凝胶电泳分析所示,所有三种修饰的果胶均与质粒DNA形成复合物。果胶-NH2 / DNA复合物的大小和形态通过透射电子显微镜(TEM)进行了检查。用人胚胎肾细胞系(HEK293)进行转染实验。使用编码绿色荧光蛋白(GFP)的质粒DNA。使用FACS通过流式细胞术分析来分析转染效率。果胶-NH2-Q是最有效的载体。向转染培养基中添加氯喹(“同质变质”剂)大大增强了HEK293转染,表明内吞作用是优选的内化途径,并暗示复合物无法逃脱内体。使用半乳糖和乳糖作为这种相互作用的竞争性抑制剂,通过抑制果胶与膜受体(半乳糖凝集素)的结合,检查了果胶对转染的贡献。结果降低了转染效率,证明了果胶的半乳糖残基对HEK293转染的重要性。暗示修饰的果胶是一种有前途的非病毒载体,可用于靶向基因递送至表面带有半乳糖结合凝集素的癌细胞。 (C)2008 Elsevier B.V.保留所有权利。

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