Extracellular Vesicles as Nanotherapeutics for Parkinson's Disease

被引:26
作者
Leggio, Loredana [1 ]
Paterno, Greta [1 ]
Vivarelli, Silvia [1 ]
L'Episcopo, Francesca [2 ]
Tirolo, Cataldo [2 ]
Raciti, Gabriele [1 ,3 ]
Pappalardo, Fabrizio [1 ]
Giachino, Carmela [2 ]
Caniglia, Salvatore [2 ]
Serapide, Maria Francesca [1 ]
Marchetti, Bianca [1 ,2 ]
Iraci, Nunzio [1 ]
机构
[1] Univ Catania, Dept Biomed & Biotechnol Sci BIOMETEC, Torre Biol, Via Santa Sofia 97, I-95125 Catania, Italy
[2] IRCCS, Neuropharmacol Sect, OASI Res Inst, I-94018 Troina, Italy
[3] Mediterranean Inst Oncol, I-95029 Catania, Italy
关键词
Parkinson's disease; neurodegeneration; extracellular vesicles; exosomes; biomarkers; nanotherapeutics; nanodrugs; nanoparticle; cell-free therapy; INTESTINAL BACTERIAL OVERGROWTH; HELICOBACTER-PYLORI ERADICATION; ALPHA-SYNUCLEIN; STEM-CELLS; DOPAMINERGIC-NEURONS; MOUSE MODEL; TRANSGENE EXPRESSION; TRANSFERRIN RECEPTOR; TYROSINE-HYDROXYLASE; THERAPEUTIC STRATEGY;
D O I
10.3390/biom10091327
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Extracellular vesicles (EVs) are naturally occurring membranous structures secreted by normal and diseased cells, and carrying a wide range of bioactive molecules. In the central nervous system (CNS), EVs are important in both homeostasis and pathology. Through receptor-ligand interactions, direct fusion, or endocytosis, EVs interact with their target cells. Accumulating evidence indicates that EVs play crucial roles in the pathogenesis of many neurodegenerative disorders (NDs), including Parkinson ' s disease (PD). PD is the second most common ND, characterized by the progressive loss of dopaminergic (DAergic) neurons within the Substantia Nigra pars compacta (SNpc). In PD, EVs are secreted by both neurons and glial cells, with either beneficial or detrimental effects, via a complex program of cell-to-cell communication. The functions of EVs in PD range from their etiopathogenetic relevance to their use as diagnostic tools and innovative carriers of therapeutics. Because they can cross the blood-brain barrier, EVs can be engineered to deliver bioactive molecules (e.g., small interfering RNAs, catalase) within the CNS. This review summarizes the latest findings regarding the role played by EVs in PD etiology, diagnosis, prognosis, and therapy, with a particular focus on their use as novel PD nanotherapeutics.
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页码:1 / 35
页数:35
相关论文
共 277 条
[1]   Mood Effects After Deep Brain Stimulation for Parkinson's Disease: An Update [J].
Accolla, Ettore A. ;
Pollo, Claudio .
FRONTIERS IN NEUROLOGY, 2019, 10
[2]   Impact of altered phosphorylation on loss of function of juvenile Parkinsonism-associated genetic variants of the E3 ligase parkin [J].
Aguirre, Jacob D. ;
Dunkerley, Karen M. ;
Lam, Rica ;
Rusal, Michele ;
Shaw, Gary S. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2018, 293 (17) :6337-6348
[3]   Cognitive performance of GBA mutation carriers with early-onset PD The CORE-PD study [J].
Alcalay, R. N. ;
Caccappolo, E. ;
Mejia-Santana, H. ;
Tang, M. -X. ;
Rosado, L. ;
Reilly, M. Orbe ;
Ruiz, D. ;
Ross, B. ;
Verbitsky, M. ;
Kisselev, S. ;
Louis, E. ;
Comella, C. ;
Colcher, A. ;
Jennings, D. ;
Nance, M. ;
Bressman, S. ;
Scott, W. K. ;
Tanner, C. ;
Mickel, S. ;
Andrews, H. ;
Waters, C. ;
Fahn, S. ;
Cote, L. ;
Frucht, S. ;
Ford, B. ;
Rezak, M. ;
Novak, K. ;
Friedman, J. H. ;
Pfeiffer, R. ;
Marsh, L. ;
Hiner, B. ;
Siderowf, A. ;
Payami, H. ;
Molho, E. ;
Factor, S. ;
Ottman, R. ;
Clark, L. N. ;
Marder, K. .
NEUROLOGY, 2012, 78 (18) :1434-1440
[4]   Cognitive and Motor Function in Long-Duration PARKIN-Associated Parkinson Disease [J].
Alcalay, Roy N. ;
Caccappolo, Elise ;
Mejia-Santana, Helen ;
Tang, Ming Xin ;
Rosado, Llency ;
Reilly, Martha Orbe ;
Ruiz, Diana ;
Louis, Elan D. ;
Comella, Cynthia L. ;
Nance, Martha A. ;
Bressman, Susan B. ;
Scott, William K. ;
Tanner, Caroline M. ;
Mickel, Susan F. ;
Waters, Cheryl H. ;
Fahn, Stanley ;
Cote, Lucien J. ;
Frucht, Steven J. ;
Ford, Blair ;
Rezak, Michael ;
Novak, Kevin E. ;
Friedman, Joseph H. ;
Pfeiffer, Ronald F. ;
Marsh, Laura ;
Hiner, Bradley ;
Payami, Haydeh ;
Molho, Eric ;
Factor, Stewart A. ;
Nutt, John G. ;
Serrano, Carmen ;
Arroyo, Maritza ;
Ottman, Ruth ;
Pauciulo, Michael W. ;
Nichols, William C. ;
Clark, Lorraine N. ;
Marder, Karen S. .
JAMA NEUROLOGY, 2014, 71 (01) :62-67
[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]   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
[7]   Intranasal Delivery of pGDNF DNA Nanoparticles Provides Neuroprotection in the Rat 6-Hydroxydopamine Model of Parkinson's Disease [J].
Aly, Amirah E. -E. ;
Harmon, Brendan T. ;
Padegimas, Linas ;
Sesenoglu-Laird, Ozge ;
Cooper, Mark J. ;
Waszczak, Barbara L. .
MOLECULAR NEUROBIOLOGY, 2019, 56 (01) :688-701
[8]   Expression of DJ-1 in Neurodegenerative Disorders [J].
Antipova, Daria ;
Bandopadhyay, Rina .
DJ-1/PARK7 PROTEIN: PARKINSON'S DISEASE, CANCER AND OXIDATIVE STRESS-INDUCED DISEASES, 2017, 1037 :25-43
[9]   Diagnosis and Treatment of Parkinson Disease A Review [J].
Armstrong, Melissa J. ;
Okun, Michael S. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2020, 323 (06) :548-560
[10]   Fluorescence-Quenched Substrates for Quantitative Live Cell Imaging of Glucocerebrosidase Activity [J].
Ashmus, Roger A. ;
Shen, David L. ;
Vocadlo, David J. .
CHEMICAL GLYCOBIOLOGY, PT B: MONITORING GLYCANS AND THEIR INTERACTIONS, 2018, 598 :199-215