Real-time gene delivery vector tracking in the endo-lysosomal pathway of live cells

被引:27
|
作者
Suh, Junghae [1 ]
An, Yoojin [2 ]
Tang, Benjamin C. [2 ]
Dempsey, Christopher [1 ]
Huang, Feiran [1 ]
Hanes, Justin [2 ,3 ]
机构
[1] Rice Univ, Dept Bioengn, Houston, TX 77005 USA
[2] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Ctr Nanomed, Baltimore, MD 21231 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
confocal microscopy; particle tracking; endosomes; lysosomes; polyethylenimine; MULTIPLE-PARTICLE TRACKING; DEPENDENT DNA MOBILITY; INTRACELLULAR-TRANSPORT; LOCALIZATION; CHOLESTEROL; ENDOCYTOSIS; COMPLEXES; DESIGN; NANOCARRIERS; COMPARTMENTS;
D O I
10.1002/jemt.21113
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Using live-cell confocal microscopy and particle tracking technology, the simultaneous transport of intracellular vesicles of the endo-lysosomal pathway and nonviral polyethylenimine (PEI)/DNA nanocomplexes was investigated. Due to potential problems associated with the use of acid-sensitive probes in combination with a gene vector that is hypothesized to buffer the pH of intracellular vesicles, the biological location of PEI/DNA gene vectors was revealed by probing their trafficking in cells expressing fluorescent versions of either early endosome antigen 1, a protein that localizes to early endosomes, or Niemann Pick C1, a protein that localizes to late endosomes and lysosomes. Studies directly show that PEI/DNA nanoparticles are actively transported within both early and late endosomes, and display similar overall transport rates in each. Additionally, gene vector transfer between endosomes is observed. Over time post-transfection, gene vectors accumulate in late endosomes/lysosomes; however, real-time escape of vectors from membrane-bound vesicles is not observed. Microsc. Res. Tech., 2012. (c) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:691 / 697
页数:7
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