Nanoparticles isolated from blood: a reflection of vesiculability of blood cells during the isolation process

被引:49
作者
Sustar, Vid [1 ]
Bedina-Zavec, Apolonija [1 ,2 ]
Stukelj, Roman [1 ]
Frank, Mojca [3 ]
Bobojevic, Goran [1 ]
Jansa, Rado [4 ]
Ogorevc, Eva [5 ]
Kruljc, Peter [6 ]
Mam, Keriya [7 ]
Simunic, Bostjan [8 ]
Mancek-Keber, Mateja [9 ]
Jerala, Roman [9 ]
Rozman, Blaz [3 ]
Veranic, Peter [10 ]
Hagerstrand, Henry [11 ]
Kralj-Iglic, Veronika [1 ]
机构
[1] Univ Ljubljana, Lab Clin Biophys, Fac Med, SI-1000 Ljubljana, Slovenia
[2] Natl Inst Chem, Lab Biosynth & Biotransformat, Ljubljana, Slovenia
[3] Ljubljana Univ Med Ctr, Dept Rheumatol, Ljubljana, Slovenia
[4] Ljubljana Univ Med Ctr, Dept Gastroenterol, Ljubljana, Slovenia
[5] Univ Ljubljana, Biophys Lab, Fac Elect Engn, SI-1000 Ljubljana, Slovenia
[6] Univ Ljubljana, Clin Reprod & Horses, Fac Vet Med, SI-1000 Ljubljana, Slovenia
[7] FEI Quanta, Eindhoven, Netherlands
[8] Natl Inst Chem, Biotechnol Lab, Ljubljana, Slovenia
[9] Univ Primorska, Sci & Res Ctr Koper, Koper, Slovenia
[10] Univ Ljubljana, Inst Cell Biol, Fac Med, SI-1000 Ljubljana, Slovenia
[11] Abo Akad Univ, Dept Biosci, Turku, Finland
关键词
nanoparticles; nanovesicles; microparticles; microvesicles; cell-cell communication; PLASMA-MEMBRANE FRAGMENTS; TISSUE-FACTOR; CIRCULATING MICROPARTICLES; PERIPHERAL-BLOOD; PLATELET MICROPARTICLES; MICROVESICLES; CANCER; ERYTHROCYTES; VESICLES; RELEASE;
D O I
10.2147/IJN.S24537
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Background: Shedding of nanoparticles from the cell membrane is a common process in all cells. These nanoparticles are present in body fluids and can be harvested by isolation. To collect circulating nanoparticles from blood, a standard procedure consisting of repeated centrifugation and washing is applied to the blood samples. Nanoparticles can also be shed from blood cells during the isolation process, so it is unclear whether nanoparticles found in the isolated material are present in blood at sampling or if are they created from the blood cells during the isolation process. We addressed this question by determination of the morphology and identity of nanoparticles harvested from blood. Methods: The isolates were visualized by scanning electron microscopy, analyzed by flow cytometry, and nanoparticle shapes were determined theoretically. Results: The average size of nanoparticles was about 300 nm, and numerous residual blood cells were found in the isolates. The shapes of nanoparticles corresponded to the theoretical shapes obtained by minimization of the membrane free energy, indicating that these nanoparticles can be identified as vesicles. The concentration and size of nanoparticles in blood isolates was sensitive to the temperature during isolation. We demonstrated that at lower temperatures, the nanoparticle concentration was higher, while the nanoparticles were on average smaller. Conclusion: These results indicate that a large pool of nanoparticles is produced after blood sampling. The shapes of deformed blood cells found in the isolates indicate how fragmentation of blood cells may take place. The results show that the contents of isolates reflect the properties of blood cells and their interaction with the surrounding solution (rather than representing only nanoparticles present in blood at sampling) which differ in different diseases and may therefore present a relevant clinical parameter.
引用
收藏
页码:2737 / 2748
页数:12
相关论文
共 60 条
[1]   RELEASE OF DIACYLGLYCEROL-ENRICHED VESICLES FROM ERYTHROCYTES WITH INCREASED INTRACELLULAR [CA2+] [J].
ALLAN, D ;
BILLAH, MM ;
FINEAN, JB ;
MICHELL, RH .
NATURE, 1976, 261 (5555) :58-60
[2]  
[Anonymous], OPEN AUTOIMMUN J
[3]  
[Anonymous], RADIOL ONCOL
[4]   RELEASE OF CHOLESTEROL-ENRICHED MICROVESICLES FROM HUMAN ERYTHROCYTES CAUSED BY HYPERTONIC SALINE AT LOW-TEMPERATURES [J].
ARAKI, T .
FEBS LETTERS, 1979, 97 (02) :237-240
[5]  
Arslan Cagatay, 2005, Turk J Haematol, V22, P59
[6]   Tumour-derived microvesicles carry several surface determinants and mRNA of tumour cells and transfer some of these determinants to monocytes [J].
Baj-Krzyworzeka, M ;
Szatanek, R ;
Weglarczyk, K ;
Baran, J ;
Urbanowicz, B ;
Branski, P ;
Ratajczak, MZ ;
Zembala, M .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2006, 55 (07) :808-818
[7]  
BASTIDA E, 1984, BLOOD, V64, P177
[8]   Cell-derived vesicles exposing coagulant tissue factor in saliva [J].
Berckmans, Rene J. ;
Sturk, Auguste ;
van Tienen, Laurens M. ;
Schaap, Marianne C. L. ;
Nieuwland, Rienk .
BLOOD, 2011, 117 (11) :3172-3180
[9]   SHEDDING FROM NORMAL AND CANCER-CELL SURFACES [J].
BLACK, PH .
NEW ENGLAND JOURNAL OF MEDICINE, 1980, 303 (24) :1415-1416
[10]   Platelets Amplify Inflammation in Arthritis via Collagen-Dependent Microparticle Production [J].
Boilard, Eric ;
Nigrovic, Peter A. ;
Larabee, Katherine ;
Watts, Gerald F. M. ;
Coblyn, Jonathan S. ;
Weinblatt, Michael E. ;
Massarotti, Elena M. ;
Remold-O'Donnell, Eileen ;
Farndale, Richard W. ;
Ware, Jerry ;
Lee, David M. .
SCIENCE, 2010, 327 (5965) :580-583