Mesenchymal Stem Cell-Derived Extracellular Vesicles as Therapeutics and as a Drug Delivery Platform

被引:190
作者
Baek, Gyuhyeon [1 ]
Choi, Hojun [1 ]
Kim, Youngeun [2 ]
Lee, Hai-Chon [2 ]
Choi, Chulhee [1 ,2 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, 291 Daehak Ro, Daejeon 34141, South Korea
[2] ILIAS Biol Inc, 40-20,Techno 6 Ro, Daejeon 34014, South Korea
基金
新加坡国家研究基金会;
关键词
IN-VITRO; MICROVESICLES PROTECT; EXOSOMES; REGENERATION; KIDNEY; INJURY; PHOSPHATIDYLSERINE; BIOGENESIS; INJECTION; VEHICLES;
D O I
10.1002/sctm.18-0226
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Mesenchymal stem cells (MSCs) are one of the most easily accessible stem cells that can be obtained from various human tissues. They have raised considerable interests for their potential applications in tissue repair, anti-cancer therapy, and inflammation suppression. Stem cell-based therapy was first used to treat muscular dystrophies and has been studied intensively for its efficacy in various disease models, including myocardial infarction, kidney injuries, liver injuries, and cancers. In this review, we summarized the potential mechanisms underlying MSC-derived EVs therapy as a drug delivery platform. Additionally, based on currently published data, we predicted a potential therapeutic role of cargo proteins shuttled by EVs from MSCs. These data may support the therapeutic strategy of using the MSC-derived EVs to accelerate this strategy from bench to bedside. Stem Cells Translational Medicine 2019;8:880&886
引用
收藏
页码:880 / 886
页数:7
相关论文
共 66 条
[61]
Extracellular vesicle in vivo biodistribution is determined by cell source, route of administration and targeting [J].
Wiklander, Oscar P. B. ;
Nordin, Joel Z. ;
O'Loughlin, Aisling ;
Gustafsson, Ylva ;
Corso, Giulia ;
Maeger, Imre ;
Vader, Pieter ;
Lee, Yi ;
Sork, Helena ;
Seow, Yiqi ;
Heldring, Nina ;
Alvarez-Erviti, Lydia ;
Smith, C. I. Edvard ;
Le Blanc, Katarina ;
Macchiarini, Paolo ;
Jungebluth, Philipp ;
Wood, Matthew J. A. ;
EL Andaloussi, Samir .
JOURNAL OF EXTRACELLULAR VESICLES, 2015, 4 :1-13
[62]
Virus-Mimetic Fusogenic Exosomes for Direct Delivery of Integral Membrane Proteins to Target Cell Membranes [J].
Yang, Yoosoo ;
Hong, Yeonsun ;
Nam, Gi-Hoon ;
Chung, Jin Hwa ;
Koh, Eunee ;
Kim, In-San .
ADVANCED MATERIALS, 2017, 29 (13)
[63]
Bioreactors to influence stem cell fate: Augmentation of mesenchymal stem cell signaling pathways via dynamic culture systems [J].
Yeatts, Andrew B. ;
Choquette, Daniel T. ;
Fisher, John P. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2013, 1830 (02) :2470-2480
[64]
Mesenchymal stem cell: An efficient mass producer of exosomes for drug delivery [J].
Yeo, Ronne Wee Yeh ;
Lai, Ruenn Chai ;
Zhang, Bin ;
Tan, Soon Sim ;
Yin, Yijun ;
Teh, Bao Ju ;
Lim, Sai Kiang .
ADVANCED DRUG DELIVERY REVIEWS, 2013, 65 (03) :336-341
[65]
Exosome engineering for efficient intracellular delivery of soluble proteins using optically reversible protein-protein interaction module [J].
Yim, Nambin ;
Ryu, Seung-Wook ;
Choi, Kyungsun ;
Lee, Kwang Ryeol ;
Lee, Seunghee ;
Choi, Hojun ;
Kim, Jeongjin ;
Shaker, Mohammed R. ;
Sun, Woong ;
Park, Ji-Ho ;
Kim, Daesoo ;
Heo, Won Do ;
Choi, Chulhee .
NATURE COMMUNICATIONS, 2016, 7
[66]
Mesenchymal Stem Cells Secrete Immunologically Active Exosomes [J].
Zhang, Bin ;
Yin, Yijun ;
Lai, Ruenn Chai ;
Tan, Soon Sim ;
Choo, Andre Boon Hwa ;
Lim, Sai Kiang .
STEM CELLS AND DEVELOPMENT, 2014, 23 (11) :1233-1244