Exosomes as a Nanodelivery System: a Key to the Future of Neuromedicine?

被引:216
作者
Aryani, Arian [1 ]
Denecke, Bernd [1 ]
机构
[1] Rhein Westfal TH Aachen, Interdisciplinary Ctr Clin Res Aachen IZKF Aachen, Pauwelsstr 30, D-52074 Aachen, Germany
关键词
Artificial exosome; Neurodegenerative disease; Extracellular vesicles; Multiple sclerosis; Diagnosis; MicroRNA; BRAIN-BARRIER DISRUPTION; CELL-DERIVED EXOSOMES; DENDRITIC CELLS; MAST-CELLS; TUNNELING NANOTUBES; MULTIVESICULAR BODY; ALZHEIMERS-DISEASE; TERMINAL FRAGMENTS; SECRETE EXOSOMES; SIRNA DELIVERY;
D O I
10.1007/s12035-014-9054-5
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Since the beginning of the last decade, exosomes have been of increased interest in the science community. Exosomes represent a new kind of long distance transfer of biological molecules among cells. This review provides a comprehensive overview about the construction of exosomes, their targeting and their fusion mechanisms to the recipient cells. Complementarily, the current state of research regarding the cargo of exosomes is discussed. A particular focus was placed on the role of exosomes in the central nervous system. An increasing number of physiological processes in the brain could be associated with exosomes. In this context, it is becoming more apparent that exosomes are involved in several neurological and specifically neurodegenerative diseases. The treatment of these kinds of diseases is often difficult not least because of the blood-brain barrier. Exosomes are very stable, can pass the blood-brain barrier and, therefore, reveal bright perspectives towards diagnosis and therapeutic treatments. A prerequisite for clinical applications is a standardised approach. Features necessary for a standardised diagnosis using exosomes are discussed. In therapeutic terms, exosomes represent a promising drug delivery system able to pass the blood-brain barrier. One option to overcome the disadvantages potentially associated with the use of endogenous exosomes is the design of artificial exosomes. The artificial exosomes with a clearly defined therapeutic active cargo and surface marker ensuring the specific targeting to the recipient cells is proposed as a promising approach.
引用
收藏
页码:818 / 834
页数:17
相关论文
共 169 条
[1]
Airoldi M, 2011, TUMORI, V97, P690, DOI 10.1700/1018.11082
[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]
Lysosomal dysfunction increases exosome-mediated alpha-synuclein release and transmission [J].
Alvarez-Erviti, Lydia ;
Seow, Yiqi ;
Schapira, Anthony H. ;
Gardiner, Chris ;
Sargent, Ian L. ;
Wood, Matthew J. A. ;
Cooper, J. Mark .
NEUROBIOLOGY OF DISEASE, 2011, 42 (03) :360-367
[4]
Exosomes neutralize synaptic-plasticity-disrupting activity of Aβ assemblies in vivo [J].
An, Kyongman ;
Klyubin, Igor ;
Kim, Youngkyu ;
Jung, Jung Hoon ;
Mably, Alexandra J. ;
O'Dowd, Sean T. ;
Lynch, Timothy ;
Kanmert, Daniel ;
Lemere, Cynthia A. ;
Finan, Gina M. ;
Park, Joon Won ;
Kim, Tae-Wan ;
Walsh, Dominic M. ;
Rowan, Michael J. ;
Kim, Joung-Hun .
MOLECULAR BRAIN, 2013, 6
[5]
Auletta JJ, 2012, IMMUNOTHERAPY-UK, V4, P529, DOI [10.2217/IMT.12.41, 10.2217/imt.12.41]
[6]
Mesenchymal stem cell secreted vesicles provide novel opportunities in (stem) cell-free therapy [J].
Baglio, Serena Rubina ;
Pegtel, D. Michiel ;
Baldini, Nicola .
FRONTIERS IN PHYSIOLOGY, 2012, 3
[7]
Human Bone Marrow-Derived Mesenchymal Stem Cells Induce Th2-Polarized Immune Response and Promote Endogenous Repair in Animal Models of Multiple Sclerosis [J].
Bai, Lianhua ;
Lennon, Donald P. ;
Eaton, Valerie ;
Maier, Kari ;
Caplan, Arnold I. ;
Miller, Stephen D. ;
Miller, Robert H. .
GLIA, 2009, 57 (11) :1192-1203
[8]
Inhibition of Myelin Membrane Sheath Formation by Oligodendrocyte-derived Exosome-like Vesicles [J].
Bakhti, Mostafa ;
Winter, Christine ;
Simons, Mikael .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (01) :787-796
[9]
Cellular basis of Alzheimers disease [J].
Bali, Jitin ;
Ben Halima, Saoussen ;
Felmy, Boas ;
Goodger, Zoe ;
Zurbriggen, Sebastian ;
Rajendran, Lawrence .
ANNALS OF INDIAN ACADEMY OF NEUROLOGY, 2010, 13 :89-93
[10]
Mutant Copper-Zinc Superoxide Dismutase (SOD1) Induces Protein Secretion Pathway Alterations and Exosome Release in Astrocytes IMPLICATIONS FOR DISEASE SPREADING AND MOTOR NEURON PATHOLOGY IN AMYOTROPHIC LATERAL SCLEROSIS [J].
Basso, Manuela ;
Pozzi, Silvia ;
Tortarolo, Massimo ;
Fiordaliso, Fabio ;
Bisighini, Cinzia ;
Pasetto, Laura ;
Spaltro, Gabriella ;
Lidonnici, Dario ;
Gensano, Francesco ;
Battaglia, Elisa ;
Bendotti, Caterina ;
Bonetto, Valentina .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (22) :15699-15711