Microparticles in stored red blood cells: an approach using flow cytometry and proteomic tools

被引:144
作者
Rubin, O. [1 ]
Crettaz, D. [1 ]
Canellini, G. [1 ]
Tissot, J. -D. [1 ]
Lion, N. [1 ,2 ]
机构
[1] Serv Reg Vaudois Transfus Sanguine, CH-1005 Lausanne, Switzerland
[2] Ecole Polytech Fed Lausanne, Lab Electrochim Phys & Analyt, Lausanne, Switzerland
关键词
blood product storage; microparticles; proteomics; red blood cells; transfusion;
D O I
10.1111/j.1423-0410.2008.01101.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and Objectives Microparticles (MPs) are small phospholipid vesicles of less than 1 mu m, shed in blood flow by various cell types. These MPs are involved in several biological processes and diseases. MPs have also been detected in blood products; however, their role in transfused patients is unknown. The purpose of this study was to characterize those MPs in blood bank conditions. Materials and Methods Qualitative and quantitative experiments using flow cytometry or proteomic techniques were performed on MPs derived from erythrocytes concentrates. In order to count MPs, they were either isolated by various centrifugation procedures or counted directly in erythrocyte concentrates. Results A 20-fold increase after 50 days of storage at 4 degrees C was observed (from 3370 +/- 1180 MPs/mu l at day 5 to 64 850 +/- 37 800 MPs/mu l at day 50). Proteomic analysis revealed changes of protein expression comparing MPs to erythrocyte membranes. Finally, the expression of Rh blood group antigens was shown on MPs generated during erythrocyte storage. Conclusions Our work provides evidence that storage of red blood cell is associated with the generation of MPs characterized by particular proteomic profiles. These results contribute to fundamental knowledge of transfused blood products.
引用
收藏
页码:288 / 297
页数:10
相关论文
共 45 条
[1]   Platelet-derived microparticles stimulate proliferation, survival, adhesion, and chemotaxis of hematopoietic cells [J].
Baj-Krzyworzeka, M ;
Majka, M ;
Pratico, D ;
Ratajczak, J ;
Vilaire, G ;
Kijowski, J ;
Reca, R ;
Janowska-Wieczorek, A ;
Ratajczak, MZ .
EXPERIMENTAL HEMATOLOGY, 2002, 30 (05) :450-459
[2]   High levels of circulating endothelial microparticles in patients with acute coronary syndromes [J].
Bernal-Mizrachi, L ;
Jy, W ;
Jimenez, JJ ;
Pastor, J ;
Mauro, LM ;
Horstman, LL ;
de Marchena, E ;
Ahn, YS .
AMERICAN HEART JOURNAL, 2003, 145 (06) :962-970
[3]   Platelet microparticles contain active caspase 3 [J].
Boing, Anita N. ;
Hau, Chi M. ;
Sturk, Auguste ;
Nieuwland, Rienk .
PLATELETS, 2008, 19 (02) :96-103
[4]   The proteome of red cell membranes and vesicles during storage in blood bank conditions [J].
Bosman, Giel J. C. G. M. ;
Lasonder, Edwin ;
Luten, Marleen ;
Roerdinkholder-Stoelwinder, Bregt ;
Novotny, Vera M. J. ;
Bos, Harry ;
De Grip, Willem J. .
TRANSFUSION, 2008, 48 (05) :827-835
[5]  
BOSMAN GJCGM, 1988, BLOOD CELLS, V14, P19
[6]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]   Platelet-derived microparticles induce angiogenesis and stimulate post-ischemic revascularization [J].
Brill, A ;
Dashevsky, O ;
Rivo, J ;
Gozal, Y ;
Varon, D .
CARDIOVASCULAR RESEARCH, 2005, 67 (01) :30-38
[8]   Lysophosphatidic acid induces thrombogenic activity through phosphatidylserine exposure and procoagulant microvesicle generation in human erythrocytes [J].
Chung, Seung-Min ;
Bae, Ok-Nam ;
Lim, Kyung-Min ;
Noh, Ji-Yoon ;
Lee, Moo-Yeol ;
Jung, Yi-Sook ;
Chung, Jin-Ho .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2007, 27 (02) :414-421
[9]   Protein kinase C activation induces phosphatidylserine exposure on red blood cells [J].
de Jong, K ;
Rettig, MP ;
Low, PS ;
Kuypers, FA .
BIOCHEMISTRY, 2002, 41 (41) :12562-12567
[10]   Tissue-factor-bearing microvesicles arise from lipid rafts and fuse with activated platelets to initiate coagulation [J].
del Conde, I ;
Shrimpton, CN ;
Thiagarajan, P ;
López, JA .
BLOOD, 2005, 106 (05) :1604-1611