Native and bioengineered extracellular vesicles for cardiovascular therapeutics

被引:418
作者
de Abreu, Ricardo Cerqueira [1 ,2 ,3 ]
Fernandes, Hugo [4 ]
Martins, Paula A. da Costa [1 ,2 ]
Sahoo, Susmita [5 ]
Emanueli, Costanza [6 ]
Ferreira, Lino [3 ,4 ]
机构
[1] Maastricht Univ, Fac Hlth Med & Life Sci, CARIM Sch Cardiovasc Dis, Maastricht, Netherlands
[2] Maastricht Univ, Fac Sci & Engn, Dept Mol Genet, Maastricht, Netherlands
[3] Univ Coimbra, CNC Ctr Neurosci & Cell Biol, Coimbra, Portugal
[4] Univ Coimbra, Fac Med, Coimbra, Portugal
[5] Icahn Sch Med Mt Sinai, Dept Med, Div Cardiol, New York, NY 10029 USA
[6] Imperial Coll London, Natl Heart & Lung Inst, London, England
关键词
CELL-DERIVED EXOSOMES; IMPROVE CARDIAC-FUNCTION; PROMOTE ANGIOGENESIS; CARDIOMYOCYTE APOPTOSIS; INDUCE ANGIOGENESIS; IN-VITRO; DELIVERY; THERAPY; BIODISTRIBUTION; MICRORNAS;
D O I
10.1038/s41569-020-0389-5
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Extracellular vesicles (EVs) are a heterogeneous group of natural particles that are relevant to the treatment of cardiovascular diseases. These endogenous vesicles have certain properties that allow them to survive in the extracellular space, bypass biological barriers and deliver their biologically active molecular cargo to recipient cells. Moreover, EVs can be bioengineered to increase their stability, bioactivity, presentation to acceptor cells and capacity for on-target binding at both cell-type-specific and tissue-specific levels. Bioengineering of EVs involves the modification of the donor cell before EV isolation or direct modification of the EV properties after isolation. The therapeutic potential of native EVs and bioengineered EVs has been only minimally explored in the context of cardiovascular diseases. Efforts to harness the therapeutic potential of EVs will require innovative approaches and a comprehensive integration of knowledge gathered from decades of research into molecular-compound delivery. In this Review, we outline the endogenous properties of EVs that make them natural delivery agents as well as the features that can be improved by bioengineering. We also discuss the therapeutic applications of native and bioengineered EVs to cardiovascular diseases and examine the opportunities and challenges that need to be addressed to advance this research area, with an emphasis on clinical translation. Extracellular vesicles are a heterogeneous group of natural particles that can deliver their biologically active molecular cargo to recipient cells. In this Review, the authors outline the endogenous properties of extracellular vesicles that make them natural delivery agents and the features that can be improved by bioengineering for the treatment of cardiovascular diseases.
引用
收藏
页码:685 / 697
页数:13
相关论文
共 174 条
[1]
Induced Pluripotent Stem Cell (iPSC)-Derived Extracellular Vesicles Are Safer and More Effective for Cardiac Repair Than iPSCs [J].
Adamiak, Marta ;
Cheng, Guangming ;
Bobis-Wozowicz, Sylwia ;
Zhao, Lin ;
Kedracka-Krok, Sylwia ;
Samanta, Anweshan ;
Karnas, Elzbieta ;
Xuan, Yu-Ting ;
Skupien-Rabian, Bozena ;
Chen, Xing ;
Jankowska, Urszula ;
Girgis, Magdy ;
Sekula, Malgorzata ;
Davani, Arash ;
Lasota, Slawomir ;
Vincent, Robert J. ;
Sarna, Michal ;
Newell, Kathy L. ;
Wang, Ou-Li ;
Dudley, Nathaniel ;
Madeja, Zbigniew ;
Dawn, Buddhadeb ;
Zuba-Surma, Ewa K. .
CIRCULATION RESEARCH, 2018, 122 (02) :296-309
[2]
Experimental, Systems, and Computational Approaches to Understanding the MicroRNA-Mediated Reparative Potential of Cardiac Progenitor Cell-Derived Exosomes From Pediatric Patients [J].
Agarwal, Udit ;
George, Alex ;
Bhutani, Srishti ;
Ghosh-Choudhary, Shohini ;
Maxwell, Joshua T. ;
Brown, Milton E. ;
Mehta, Yash ;
Platt, Manu O. ;
Liang, Yaxuan ;
Sahoo, Susmita ;
Davis, Michael E. .
CIRCULATION RESEARCH, 2017, 120 (04) :701-+
[3]
UBL3 modification influences protein sorting to small extracellular vesicles [J].
Ageta, Hiroshi ;
Ageta-Ishihara, Natsumi ;
Hitachi, Keisuke ;
Karayel, Ozge ;
Onouchi, Takanori ;
Yamaguchi, Hisateru ;
Kahyo, Tomoaki ;
Hatanaka, Ken ;
Ikegami, Koji ;
Yoshioka, Yusuke ;
Nakamura, Kenji ;
Kosaka, Nobuyoshi ;
Nakatani, Masashi ;
Uezumi, Akiyoshi ;
Ide, Tomihiko ;
Tsutsumi, Yutaka ;
Sugimura, Haruhiko ;
Kinoshita, Makoto ;
Ochiya, Takahiro ;
Mann, Matthias ;
Setou, Mitsutoshi ;
Tsuchida, Kunihiro .
NATURE COMMUNICATIONS, 2018, 9
[4]
Evaluation of desialylation effect on zeta potential of extracellular vesicles secreted from human prostate cancer cells by on-chip microcapillary electrophoresis [J].
Akagi, Takanori ;
Kato, Kei ;
Hanamura, Nami ;
Kobayashi, Masashi ;
Ichiki, Takanori .
JAPANESE JOURNAL OF APPLIED PHYSICS, 2014, 53 (06)
[5]
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
[6]
Exosome-Mediated Benefits of Cell Therapy in Mouse and Human Models of Duchenne Muscular Dystrophy [J].
Aminzadeh, Mark A. ;
Rogers, Russell G. ;
Fournier, Mario ;
Tobin, Rachel E. ;
Guan, Xuan ;
Childers, Martin K. ;
Andres, Allen M. ;
Taylor, David J. ;
Ibrahim, Ahmed ;
Ding, Xiangming ;
Torrente, Angelo ;
Goldhaber, Joshua M. ;
Lewis, Michael ;
Gottlieb, Roberta A. ;
Victor, Ronald A. ;
Marban, Eduardo .
STEM CELL REPORTS, 2018, 10 (03) :942-955
[7]
Extracellular matrix-derived extracellular vesicles promote cardiomyocyte growth and electrical activity in engineered cardiac atria [J].
An, Minae ;
Kwon, Kihwan ;
Park, Junbeom ;
Ryu, Dong-Ryeol ;
Shin, Jung-A. ;
Kang, Jihee Lee ;
Choi, Ji Ha ;
Park, Eun-Mi ;
Lee, Kyung Eun ;
Woo, Minna ;
Kim, Minsuk .
BIOMATERIALS, 2017, 146 :49-59
[8]
[Anonymous], 2016, ADV DRUG DELIV REV A
[9]
Targeting extracellular vesicles to injured tissue using membrane cloaking and surface display [J].
Antes, Travis J. ;
Middleton, Ryan C. ;
Luther, Kristin M. ;
Ijichi, Takeshi ;
Peck, Kiel A. ;
Liu, Weixin Jane ;
Valle, Jackie ;
Echavez, Antonio K. ;
Marban, Eduardo .
JOURNAL OF NANOBIOTECHNOLOGY, 2018, 16
[10]
Mesenchymal stem cell-derived exosomes increase ATP levels, decrease oxidative stress and activate PI3K/Akt pathway to enhance myocardial viability and prevent adverse remodeling after myocardial ischemia/reperfusion injury [J].
Arslan, Fatih ;
Lai, Ruenn Chai ;
Smeets, Mirjam B. ;
Akeroyd, Lars ;
Choo, Andre ;
Aguor, Eissa N. E. ;
Timmers, Leo ;
van Rijen, Harold V. ;
Doevendans, Pieter A. ;
Pasterkamp, Gerard ;
Lim, Sai Kiang ;
de Kleijn, Dominique P. .
STEM CELL RESEARCH, 2013, 10 (03) :301-312