A systematic approach to exosome-based translational nanomedicine

被引:89
作者
Hood, Joshua L. [1 ]
Wickline, Samuel A. [1 ]
机构
[1] Washington Univ, Sch Med, Consortium Translat Res Adv Imaging & Nanomed C T, Dept Med,Div Cardiol, St Louis, MO 63130 USA
关键词
TUMOR-DERIVED EXOSOMES; MESENCHYMAL STEM-CELLS; MEMBRANE-VESICLES; PROTEOMIC ANALYSIS; CANCER CELLS; GEL; MICROVESICLES; MODULATION; INDUCTION; RECEPTOR;
D O I
10.1002/wnan.1174
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
Exosomes are a type of cell-derived extracellular nanovesicle. They relay information between cells. Some known exosome functions include immune modulation, promotion of angiogenesis, and tumor metastasis. To date, clinical use of exosomes has focused predominantly on evaluating their efficacy as cancer vaccines or diagnostically as biomarker containers. However, few investigations have explored their potential to serve as a platform for the development of semi-synthetic nanovesicles. Given their nanoscale size, potential to express targeting ligands in native conformations and deformable structure, exosomes offer a logical biological vesicle platform for adapting and producing semi-synthetic vesicles with excellent potential for nanomedicine applications. However, there are obstacles associated with realizing this potential that must be addressed. Thus, a systematic approach to isolating, modifying, and testing exosomes is presented to facilitate the introduction of exosome-based translational nanomedicine. WIREs Nanomed Nanobiotechnol 2012, 4:458467. doi: 10.1002/wnan.1174 For further resources related to this article, please visit the . Hood JL and Wickline SA wrote and edited the manuscript. Hood JL is the principal investigator of the exosome project at C-TRAIN. Conflict of interest: The authors of this manuscript have no conflicts of interest to disclose.
引用
收藏
页码:458 / 467
页数:10
相关论文
共 61 条
[1]
Intercellular transfer of the oncogenic receptor EGFrvIII by microvesicles derived from tumour cells [J].
Al-Nedawi, Khalid ;
Meehan, Brian ;
Micallef, Johann ;
Lhotak, Vladimir ;
May, Linda ;
Guha, Abhijit ;
Rak, Janusz .
NATURE CELL BIOLOGY, 2008, 10 (05) :619-U24
[2]
Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes [J].
Alvarez-Erviti, Lydia ;
Seow, Yiqi ;
Yin, HaiFang ;
Betts, Corinne ;
Lakhal, Samira ;
Wood, Matthew J. A. .
NATURE BIOTECHNOLOGY, 2011, 29 (04) :341-U179
[3]
[Anonymous], Molecular Probes Handbook, A Guide to Fluorescent Probes and Labeling Technologies, V11th
[4]
[Anonymous], CURRENT PROTOCOLS CE
[5]
Morphologic and proteomic characterization of exosomes released by cultured extravillous trophoblast cells [J].
Atay, Safinur ;
Gercel-Taylor, Cicek ;
Kesimer, Mehmet ;
Taylor, Douglas D. .
EXPERIMENTAL CELL RESEARCH, 2011, 317 (08) :1192-1202
[6]
Trophoblast-Derived Exosomes Mediate Monocyte Recruitment and Differentiation [J].
Atay, Safinur ;
Gercel-Taylor, Cicek ;
Suttles, Jill ;
Mor, Gil ;
Taylor, Douglas D. .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2011, 65 (01) :65-77
[7]
Exosomes from breast cancer cells can convert adipose tissue-derived mesenchymal stem cells into myofibroblast-like cells [J].
Cho, Jung Ah ;
Park, Ho ;
Lim, Eun Hye ;
Lee, Kyo Won .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2012, 40 (01) :130-138
[8]
Exosomes from ovarian cancer cells induce adipose tissue-derived mesenchymal stem cells to acquire the physical and functional characteristics of tumor-supporting myofibroblasts [J].
Cho, Jung Ah ;
Park, Ho ;
Lim, Eun Hye ;
Kim, Kye Hyun ;
Choi, Joong Sub ;
Lee, Jung Hoon ;
Shin, Jae Wook ;
Lee, Kyo Won .
GYNECOLOGIC ONCOLOGY, 2011, 123 (02) :379-386
[9]
Adhesion and signaling by B cell-derived exosomes: the role of integrins [J].
Clayton, A ;
Turkes, A ;
Dewitt, S ;
Steadman, R ;
Mason, MD ;
Hallett, MB .
FASEB JOURNAL, 2004, 18 (06) :977-+
[10]
Shedding microvesicles: artefacts no more [J].
Cocucci, Emanuele ;
Racchetti, Gabriella ;
Meldolesi, Jacopo .
TRENDS IN CELL BIOLOGY, 2009, 19 (02) :43-51