Cell-derived vesicles for drug therapy and diagnostics: Opportunities and challenges

被引:149
作者
Fuhrmann, Gregor [1 ,2 ,3 ]
Herrmann, Inge K. [1 ,2 ,3 ]
Stevens, Molly M. [1 ,2 ,3 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Mat, London SW7 2AZ, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Bioengn, London SW7 2AZ, England
[3] Univ London Imperial Coll Sci Technol & Med, Inst Biomed Engn, London SW7 2AZ, England
基金
英国惠康基金; 瑞士国家科学基金会;
关键词
Exosomes; Microvesicles; Drug targeting; Minimally invasive diagnostics; EXOSOME-MIMETIC NANOVESICLES; EXTRACELLULAR VESICLES; HORIZONTAL TRANSFER; MEMBRANE-VESICLES; TISSUE FACTOR; MICROVESICLES; DELIVERY; MICRORNA; SIRNA; RNA;
D O I
10.1016/j.nantod.2015.04.004
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Extracellular vesicles are small lipid-based membrane-bound entities shed by cells under both physiological and pathological conditions. Their discovery as intercellular communicators through transfer of nucleic acid- and protein-based cargos between cells locally and at distance in a highly specific manner has created recent excitement. The information they transport and their composition may vary depending on the cell of origin as well as the eliciting stimulus. Such sensitive changes in vesicle characteristics hold significant promise for the improved diagnosis of pathological conditions, including infections and neoplastic lesions in a minimally invasive way. Similarly, these cell-derived vesicles exhibit promising characteristics that could enhance drug targeting efficiencies. Recent developments in the field have aimed at studying EVs as novel drug carriers due to their natural composition, biological function and selective cell interaction. In this review, we discuss new research avenues in diagnostics and drug therapy based on extracellular vesicles. We show how cell-derived vesicles can be harvested and engineered to meet application-specific design requirements. We finally discuss potential risks encountered when translating extracellular vesicle based approaches into (pre)clinical applications. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:397 / 409
页数:13
相关论文
共 91 条
[81]
Plasma exosomes can deliver exogenous short interfering RNA to monocytes and lymphocytes [J].
Wahlgren, Jessica ;
Karlson, Tanya De L. ;
Brisslert, Mikael ;
Sani, Forugh Vaziri ;
Telemo, Esbjorn ;
Sunnerhagen, Per ;
Valadi, Hadi .
NUCLEIC ACIDS RESEARCH, 2012, 40 (17)
[82]
Cardiomyocyte Microvesicles Contain DNA/RNA and Convey Biological Messages to Target Cells [J].
Waldenstrom, Anders ;
Genneback, Nina ;
Hellman, Urban ;
Ronquist, Gunnar .
PLOS ONE, 2012, 7 (04)
[83]
Standardization of sample collection, isolation and analysis methods in extracellular vesicle research [J].
Witwer, Kenneth W. ;
Buzas, Edit I. ;
Bemis, Lynne T. ;
Bora, Adriana ;
Lasser, Cecilia ;
Lotvall, Jan ;
Hoen, Esther N. Nolte-'t ;
Piper, Melissa G. ;
Sivaraman, Sarada ;
Skog, Johan ;
Thery, Clotilde ;
Wauben, Marca H. ;
Hochberg, Fred .
JOURNAL OF EXTRACELLULAR VESICLES, 2013, 2 (01)
[84]
Tumor-derived exosomes are a source of shared tumor rejection antigens for CTL cross-priming [J].
Wolfers, J ;
Lozier, A ;
Raposo, G ;
Regnault, A ;
Théry, C ;
Masurier, C ;
Flament, C ;
Pouzieux, S ;
Faure, F ;
Tursz, T ;
Angevin, E ;
Amigorena, S ;
Zitvogel, L .
NATURE MEDICINE, 2001, 7 (03) :297-303
[85]
Lung cancer secreted microvesicles: Underappreciated modulators of microenvironment in expanding tumors [J].
Wysoczynski, Marcin ;
Ratajczak, Mariusz Z. .
INTERNATIONAL JOURNAL OF CANCER, 2009, 125 (07) :1595-1603
[86]
Microvesicles at the Crossroads Between Infection and Cardiovascular Diseases [J].
Xiong, Jing ;
Miller, Virginia M. ;
Li, Yunman ;
Jayachandran, Muthuvel .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2012, 59 (02) :124-132
[87]
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
[88]
Non-viral vectors for gene-based therapy [J].
Yin, Hao ;
Kanasty, Rosemary L. ;
Eltoukhy, Ahmed A. ;
Vegas, Arturo J. ;
Dorkin, J. Robert ;
Anderson, Daniel G. .
NATURE REVIEWS GENETICS, 2014, 15 (08) :541-555
[89]
Secreted Monocytic miR-150 Enhances Targeted Endothelial Cell Migration [J].
Zhang, Yujing ;
Liu, Danqing ;
Chen, Xi ;
Li, Jing ;
Li, Limin ;
Bian, Zhen ;
Sun, Fei ;
Lu, Jiuwei ;
Yin, Yuan ;
Cai, Xing ;
Sun, Qi ;
Wang, Kehui ;
Ba, Yi ;
Wang, Qiang ;
Wang, Dongjin ;
Yang, Junwei ;
Liu, Pingsheng ;
Xu, Tao ;
Yan, Qiao ;
Zhang, Junfeng ;
Zen, Ke ;
Zhang, Chen-Yu .
MOLECULAR CELL, 2010, 39 (01) :133-144
[90]
Treatment of Brain Inflammatory Diseases by Delivering Exosome Encapsulated Anti-inflammatory Drugs From the Nasal Region to the Brain [J].
Zhuang, Xiaoying ;
Xiang, Xiaoyu ;
Grizzle, William ;
Sun, Dongmei ;
Zhang, Shuangqin ;
Axtell, Robert C. ;
Ju, Songwen ;
Mu, Jiangyao ;
Zhang, Lifeng ;
Steinman, Lawrence ;
Miller, Donald ;
Zhang, Huang-Ge .
MOLECULAR THERAPY, 2011, 19 (10) :1769-1779