Cellular Engineering with Membrane Fusogenic Liposomes to Produce Functionalized Extracellular Vesicles

被引:118
作者
Lee, Junsung [1 ,2 ,3 ]
Lee, Hyoungjin [1 ,3 ]
Goh, Unbyeol [1 ,3 ]
Kim, Jiyoung [1 ,3 ]
Jeong, Moonkyoung [1 ,3 ]
Lee, Jean [1 ,3 ]
Park, Ji-Ho [1 ,2 ,3 ,4 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Daejeon 34141, South Korea
[2] Korea Adv Inst Sci & Technol, Grad Sch Med Sci & Engn, Daejeon 34141, South Korea
[3] Korea Adv Inst Sci & Technol, Inst Hlth Sci & Technol, Daejeon 34141, South Korea
[4] Korea Adv Inst Sci & Technol, Inst Nanocentury, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
cellular engineering click chemistry; drug delivery; extracellular vesicle; liposome; BREAST-CANCER CELLS; EXOSOMES; DELIVERY; ELECTROPORATION; STABILITY; MECHANISM; THERAPY; BRAIN; SIRNA;
D O I
10.1021/acsami.6b01315
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Engineering of extracellular vesicles (EVs) without affecting biological functions remains a challenge, limiting the broad applications of EVs in biomedicine. Here, we report a method to equip EVs with various functional agents, including fluorophores, drugs, lipids, and bio-orthogonal chemicals, in an efficient and controlled manner by engineering parental cells with membrane fusogenic liposomes, while keeping the EVs intact. As a demonstration of how this method can be applied, we prepared EVs containing azide-lipids, and conjugated them with targeting peptides using copper-free click chemistry to enhance targeting efficacy to cancer cells. We believe that this liposome-based cellular engineering method will find utility in studying the biological roles of EVs and delivering therapeutic agents through their innate pathway.
引用
收藏
页码:6790 / 6795
页数:6
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