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基于三油酸甘油酯的阳离子脂质纳米载体用于高效基因传递:特性和机制。

Triolein-based polycation lipid nanocarrier for efficient gene delivery: characteristics and mechanism.

机构信息

Key Laboratory of Smart Drug Delivery, Ministry of Education and PLA, Department of Pharmaceutics, School of Pharmacy, Fudan University, Shanghai, People's Republic of China.

出版信息

Int J Nanomedicine. 2011;6:2235-44. doi: 10.2147/IJN.S24720. Epub 2011 Oct 7.

Abstract

We proposed to develop a polycation lipid nanocarrier (PLN) with higher transfection efficiency than our previously described polycation nanostrucutred lipid nanocarrier (PNLC). PLN was composed of triolein, cetylated low-molecular-weight polyethylenimine, and dioleoyl phosphatidylethanolamine. The physicochemical properties of PLN and the PLN/DNA complexes (PDC) were characterized. The in vitro transfection was performed in human lung adenocarcinoma (SPC-A1) cells, and the intracellular mechanism was investigated as well. The measurements indicated that PLN and PDC are homogenous nanometer-sized particles with a positive charge. The transfection efficiency of PDC significantly increased with the content of triolein and was higher than that of PNLC and commercial Lipofectamine 2000. In particular, the transfection of PLN in the presence of 10% serum was more effective than that in its absence. With the help of specific inhibitors of chlorpromazine and filipin, the clathrin-dependent endocytosis pathway was determined to be the main contributor to the successful transfection mediated by PLN in SPC-A1 cells. The captured images verified that the fluorescent PDC was localized in the lysosomes and nuclei after endocytosis. Thus, PLN represents a novel efficient nonviral gene delivery vector.

摘要

我们提出开发一种阳离子脂质纳米载体(PLN),其转染效率高于我们之前描述的阳离子纳米结构脂质纳米载体(PNLC)。PLN 由三油酸甘油酯、酯化低分子量聚乙二胺和二油酰基磷脂酰乙醇胺组成。对 PLN 和 PLN/DNA 复合物(PDC)的理化性质进行了表征。在人肺腺癌细胞(SPC-A1)中进行了体外转染,并研究了其细胞内机制。测量结果表明,PLN 和 PDC 是均一的纳米级带正电荷的颗粒。PDC 的转染效率随着三油酸甘油酯含量的增加而显著提高,高于 PNLC 和商业 Lipofectamine 2000。特别是,在存在 10%血清的情况下,PLN 的转染比不存在血清时更有效。在氯丙嗪和 Filipin 特异性抑制剂的帮助下,确定网格蛋白依赖的内吞途径是 PLN 在 SPC-A1 细胞中介导成功转染的主要途径。摄取的图像证实,荧光 PDC 在被内吞后定位于溶酶体和细胞核中。因此,PLN 代表一种新型有效的非病毒基因传递载体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4ef/3215164/4022b336f645/ijn-6-2235f1.jpg

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