Platelet apoptosis and activation in platelet concentrates stored for up to 12 days in plasma or additive solution

被引:43
作者
Cookson, P. [1 ]
Sutherland, J. [2 ]
Turner, C. [1 ]
Bashir, S. [1 ]
Wiltshire, M. [1 ]
Hancock, V. [1 ]
Smith, K. [1 ]
Cardigan, R. [1 ]
机构
[1] NHS Blood & Transplant, Components Dev Lab, Brentwood CM15 8DP, Essex, England
[2] Natl Inst Biol Stand & Controls, Potters Bar EN6 3QG, Herts, England
关键词
extended storage; platelet apoptosis; storage media; PERMEABILITY TRANSITION PORE; GLYCOPROTEIN-IB-ALPHA; IN-VITRO FUNCTION; CELL-DEATH; STORAGE; VIVO; CASPASE; PHAGOCYTOSIS; TRANSFUSION; APHERESIS;
D O I
10.1111/j.1365-3148.2010.01034.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Study design and methods: Pooled buffy coat PC (n = 7) were prepared in either 100% plasma or 70% Composol and stored at 22 degrees C for 12 days. A third arm of the study stored PC in 100% plasma at 37 degrees C, which is thought to induce apoptosis. PC were tested for mitochrondrial membrane potential, annexin V binding, microparticles, caspase-3/7 activity and decoy cell death receptor 2, as well as standard platelet quality tests. Results: Composol units remained >= pH 6 center dot 88, with 36% lower lactate and higher pH vs plasma by day 12 (P < 0 center dot 001). Platelet function was better maintained, and activation and apoptotic markers tended to be lower in Composol units towards the end of storage. However, levels of all apoptosis markers assessed were not significantly different in units stored in Composol. Storage at 37 degrees C saw stronger correlation of apoptotic markers with standard quality tests compared to 22 degrees C, but loss of correlation of caspase-3/7 activity with other apoptosis markers. Conclusion: We conclude that storage of platelets in 70% Composol vs 100% plasma does not increase the rate of platelet apoptosis. Our data agree with other studies suggesting that platelet apoptosis is sequential to high levels of activation, but share a significant degree of overlap.
引用
收藏
页码:392 / 402
页数:11
相关论文
共 47 条
[21]  
LEUNG R, 2003, J THROMB HAEMOST S, V1, pP213
[22]   Higher thrombin concentrations are required to induce platelet apoptosis than to induce platelet activation [J].
Leytin, V. ;
Allen, D. J. ;
Lyubimov, E. ;
Freedman, J. .
BRITISH JOURNAL OF HAEMATOLOGY, 2007, 136 (05) :762-764
[23]   Thrombin-triggered platelet apoptosis [J].
Leytin, V. ;
Allen, D. J. ;
Mykhaylov, S. ;
Lyubimov, E. ;
Freedman, J. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2006, 4 (12) :2656-2663
[24]   Role of platelet surface glycoprotein Ibα and P-selectin in the clearance of transfused platelet concentrates [J].
Leytin, V ;
Allen, DJ ;
Gwozdz, A ;
Garvey, B ;
Freedman, J .
TRANSFUSION, 2004, 44 (10) :1487-1495
[25]   Pathologic high shear stress induces apoptosis events in human platelets [J].
Leytin, V ;
Allen, DJ ;
Mykhaylov, S ;
Mis, L ;
Lyubimov, EV ;
Garvey, B ;
Freedman, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 320 (02) :303-310
[26]   Platelet activation and apoptosis are different phenomena: evidence from the sequential dynamics and the magnitude of responses during platelet storage [J].
Leytin, Valery ;
Allen, David J. ;
Mutlu, Asuman ;
Mykhaylov, Sergiy ;
Lyubimov, Elena ;
Freedman, John .
BRITISH JOURNAL OF HAEMATOLOGY, 2008, 142 (03) :494-497
[27]   Mitochondrial control of platelet apoptosis: effect of cyclosporin A, an inhibitor of the mitochondrial permeability transition pore [J].
Leytin, Valery ;
Allen, David J. ;
Mutlu, Asuman ;
Gyulkhandanyan, Armen V. ;
Mykhaylov, Sergiy ;
Freedman, John .
LABORATORY INVESTIGATION, 2009, 89 (04) :374-384
[28]   Programmed anuclear cell death delimits platelet life span [J].
Mason, Kylie D. ;
Carpinelli, Marina R. ;
Fletcher, Jamie I. ;
Collinge, Janelle E. ;
Hilton, Adrienne A. ;
Ellis, Sarah ;
Kelly, Priscilla N. ;
Ekert, Paul G. ;
Metcalf, Donald ;
Roberts, Andrew W. ;
Huang, David C. S. ;
Kile, Benjamin T. .
CELL, 2007, 128 (06) :1173-1186
[29]   Decreased platelet aggregation of platelet concentrate during storage recovers in the body after transfusion [J].
Miyaji, R ;
Sakai, M ;
Urano, H ;
Nakata, K ;
Sakamoto, H ;
Shirahata, A .
TRANSFUSION, 2004, 44 (06) :891-899
[30]  
Murphy S, 2004, TRANSFUSION, V44, P618, DOI 10.1111/j.1537-2995.2004.00355.x