Isolation and Characterization of Small Extracellular Vesicles from Porcine Blood Plasma, Cerebrospinal Fluid, and Seminal Plasma

被引:49
作者
Skalnikova, Helena Kupcova [1 ]
Bohuslavova, Bozena [1 ]
Turnovcova, Karolina [1 ,2 ]
Juhasova, Jana [1 ]
Juhas, Stefan [1 ]
Rodinova, Marie [1 ,3 ,4 ]
Vodicka, Petr [1 ]
机构
[1] Czech Acad Sci, Inst Anim Physiol & Genet, Rumburska 89, Libechov 27721, Czech Republic
[2] Czech Acad Sci, Inst Expt Med, Videnska 1083, Prague 14220, Czech Republic
[3] Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Ke Karlovu 2, Prague 12109, Czech Republic
[4] Gen Univ Hosp Prague, Ke Karlovu 2, Prague 12109, Czech Republic
关键词
extracellular vesicle; exosome; body fluid; plasma; cerebrospinal fluid; seminal plasma; pig model; proteomics; PROTEOMIC ANALYSIS; BODY-FLUIDS; EXOSOMES; IDENTIFICATION; MODEL; MATURATION; SECRETION; PROTEINS; DISEASE;
D O I
10.3390/proteomes7020017
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 a highly attractive subject of biomedical research as possible carriers of nucleic acid and protein biomarkers. EVs released to body fluids enable indirect access to inner organs by so-called liquid biopsies. Obtaining a high-quality EV sample with minimum contaminants is crucial for proteomic analyses using LC-MS/MS or other techniques. However, the EV content in various body fluids largely differs, which may hamper subsequent analyses. Here, we present a comparison of extracellular vesicle yields from blood plasma, cerebrospinal fluid, and seminal plasma using an experimental pig model. Pigs are widely used in biomedical research as large animal models with anatomy and physiology close to those of humans and enable studies (e.g., of the nervous system) that are unfeasible in humans. EVs were isolated from body fluids by differential centrifugation followed by ultracentrifugation. EVs were characterized according to protein yields and to the quality of the isolated vesicles (e.g., size distribution, morphology, positivity for exosome markers). In our experimental setting, substantial differences in EV amounts were identified among body fluids, with the seminal plasma being the richest EV source. The yields of pellet proteins from ultracentrifugation of 1 mL of porcine body fluids may help to estimate body fluid input volumes to obtain sufficient samples for subsequent proteomic analyses.
引用
收藏
页数:14
相关论文
共 53 条
[1]   The impact of various preanalytical treatments on the phenotype of small extracellular vesicles in blood analyzed by protein microarray [J].
Baek, Rikke ;
Sondergaard, Evo K. L. ;
Varming, Kim ;
Jorgensen, Malene M. .
JOURNAL OF IMMUNOLOGICAL METHODS, 2016, 438 :11-20
[2]   Isolation of Exosomes from Blood Plasma: Qualitative and Quantitative Comparison of Ultracentrifugation and Size Exclusion Chromatography Methods [J].
Baranyai, Tamas ;
Herczeg, Kata ;
Onodi, Zsofia ;
Voszka, Istvan ;
Modos, Karoly ;
Marton, Nikolett ;
Nagy, Gyoergy ;
Maeger, Imre ;
Wood, Matthew J. ;
El Andaloussi, Samir ;
Palinkas, Zoltan ;
Kumar, Vikas ;
Nagy, Pater ;
Kittel, Agnes ;
Buzas, Edit Iren ;
Ferdinandy, Peter ;
Giricz, Zoltan .
PLOS ONE, 2015, 10 (12)
[3]   Extracellular Vesicle-Mediated Cell-Cell Communication in the Nervous System: Focus on Neurological Diseases [J].
Bavisotto, Celeste Caruso ;
Scalia, Federica ;
Gammazza, Antonella Marino ;
Carlisi, Daniela ;
Bucchieri, Fabio ;
de Macario, Everly Conway ;
Macario, Alberto J. L. ;
Cappello, Francesco ;
Campanella, Claudia .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (02)
[4]   A Transgenic Minipig Model of Huntington's Disease [J].
Baxa, Monika ;
Hruska-Plochan, Marian ;
Juhas, Stefan ;
Vodicka, Petr ;
Pavlok, Antonin ;
Juhasova, Jana ;
Miyanohara, Atsushi ;
Nejime, Tetsuya ;
Klima, Jiri ;
Macakova, Monika ;
Marsala, Silvia ;
Weiss, Andreas ;
Kubickova, Svatava ;
Musilova, Petra ;
Vrtel, Radek ;
Sontag, Emily M. ;
Thompson, Leslie M. ;
Schier, Jan ;
Hansikova, Hana ;
Howland, David S. ;
Cattaneo, Elena ;
DiFiglia, Marian ;
Marsala, Martin ;
Motlik, Jan .
JOURNAL OF HUNTINGTONS DISEASE, 2013, 2 (01) :47-68
[5]   Biochemical characterization of a new melanoma model the minipig MeLiM strain [J].
Borovansky, J ;
Horák, V ;
Elleder, M ;
Fortyn, K ;
Smit, NPM ;
Kolb, AM .
MELANOMA RESEARCH, 2003, 13 (06) :543-548
[6]   Immunoaffinity based methods are superior to kits for purification of prostate derived extracellular vesicles from plasma samples [J].
Brett, Sabine I. ;
Lucien, Fabrice ;
Guo, Charles ;
Williams, Karla C. ;
Kim, Yohan ;
Durfee, Paul N. ;
Brinker, C. J. ;
Chin, Joseph I. ;
Yang, Jun ;
Leong, Hon S. .
PROSTATE, 2017, 77 (13) :1335-1343
[7]   On the Choice of the Extracellular Vesicles for Therapeutic Purposes [J].
Campanella, Claudia ;
Bavisotto, Celeste Caruso ;
Logozzi, Mariantonia ;
Gammazza, Antonella Marino ;
Mizzoni, Davide ;
Cappello, Francesco ;
Fais, Stefano .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (02)
[8]   Microparticle counts in platelet-rich and platelet-free plasma, effect of centrifugation and sample-processing protocols [J].
Chandler, Wayne L. .
BLOOD COAGULATION & FIBRINOLYSIS, 2013, 24 (02) :125-132
[9]   Proteomic analysis of cerebrospinal fluid extracellular vesicles: A comprehensive dataset [J].
Chiasserini, Davide ;
van Weering, Jan R. T. ;
Piersma, Sander R. ;
Pham, Thang V. ;
Malekzadeh, Arjan ;
Teunissen, Charlotte E. ;
de Wit, Heidi ;
Jimenez, Connie R. .
JOURNAL OF PROTEOMICS, 2014, 106 :191-204
[10]   Extracellular vesicles - Their role in the packaging and spread of misfolded proteins associated with neurodegenerative diseases [J].
Coleman, Bradley M. ;
Hill, Andrew F. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2015, 40 :89-96