RETRACTED: De novo protein synthesis in mature platelets: a consideration for transfusion medicine (Retracted article. See JUN, 2023)

被引:65
作者
Schubert, P. [1 ]
Devine, D. V. [1 ]
机构
[1] Univ British Columbia, Canadian Blood Serv, Ctr Blood Res, Vancouver, BC V6T 1Z3, Canada
基金
加拿大创新基金会; 加拿大健康研究院;
关键词
blood platelet; platelet quality; protein synthesis; proteomics; transcription; transfusion; translation; MESSENGER-RNA; ACTIVATED PLATELETS; TISSUE FACTOR; PATHOGEN INACTIVATION; TRANSLATIONAL CONTROL; PROTEOMIC ANALYSIS; SERIAL ANALYSIS; GENE; EXPRESSION; PHOSPHORYLATION;
D O I
10.1111/j.1423-0410.2010.01333.x
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Platelet function in thrombosis and haemostasis is reasonably well understood at the molecular level with respect to the proteins involved in cellular structure, signalling networks and platelet interaction with clotting factors and other cells. However, the natural history of these proteins has only recently garnered the attention of platelet researchers. De novo protein synthesis in platelets was discovered 40 years ago; however, it was generally dismissed as merely an interesting minor phenomenon until studies over the past few years renewed interest in this aspect of platelet proteins. It is now accepted that anucleate platelets not only have the potential to synthesize proteins, but this capacity seems to be required to fulfil their function. With translational control as the primary mode of regulation, platelets are able to express biologically relevant gene products in a timely and signal-dependent manner. Platelet protein synthesis during storage of platelet concentrates is a nascent area of research. Protein synthesis does occur, although not for all proteins found in the platelet protein profile. Furthermore, mRNA appears to be well preserved under standard storage conditions. Although its significance is not yet understood, the ability to replace proteins may form a type of cellular repair mechanism during storage. Disruption by inappropriate storage conditions or processes that block protein synthesis such as pathogen reduction technologies may have direct effects on the ability of platelets to synthesize proteins during storage.
引用
收藏
页码:112 / 122
页数:11
相关论文
共 83 条
[1]
Yeast Pab1 interacts with Rna15 and participates in the control of the poly(A) tail length in vitro [J].
Amrani, N ;
Minet, M ;
LeGouar, M ;
Lacroute, F ;
Wyers, F .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (07) :3694-3701
[2]
Enhancement of human platelet aggregation and secretion induced by rapamycin [J].
Babinska, A ;
Markell, MS ;
Salifu, MO ;
Akoad, M ;
Ehrlich, YH ;
Kornecki, E .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1998, 13 (12) :3153-3159
[3]
BELLOC F, 1982, NOUV REV FR HEMATOL, V24, P369
[4]
STUDIES ON HUMAN PLATELETS .1. SYNTHESIS OF PLATELET PROTEIN IN A CELL-FREE SYSTEM [J].
BOOYSE, FM ;
RAFELSON, ME .
BIOCHIMICA ET BIOPHYSICA ACTA, 1968, 166 (03) :689-&
[5]
STUDIES ON HUMAN PLATELETS .2. PROTEIN SYNTHETIC ACTIVITY OF VARIOUS PLATELET POPULATIONS [J].
BOOYSE, FM ;
HOVEKE, TP ;
RAFELSON, ME .
BIOCHIMICA ET BIOPHYSICA ACTA, 1968, 157 (03) :660-&
[6]
Platelets synthesize large amounts of active plasminogen activator inhibitor 1 [J].
Brogren, H ;
Karlsson, L ;
Andersson, M ;
Wang, LW ;
Erlinge, D ;
Jern, S .
BLOOD, 2004, 104 (13) :3943-3948
[7]
THE EFFECT OF CHLORAMPHENICOL AND CYCLOHEXIMIDE ON PLATELET-AGGREGATION AND PROTEIN-SYNTHESIS [J].
BRUCE, IJ ;
KERRY, R .
BIOCHEMICAL PHARMACOLOGY, 1987, 36 (11) :1769-1773
[8]
Characterization of the proteins released from activated platelets leads to localization of novel platelet proteins in human atherosclerotic lesions [J].
Coppinger, JA ;
Cagney, G ;
Toomey, S ;
Kislinger, T ;
Belton, O ;
McRedmond, JP ;
Cahill, DJ ;
Emili, A ;
Fitzgerald, DJ ;
Maguire, PB .
BLOOD, 2004, 103 (06) :2096-2104
[9]
Escaping the nuclear confines: Signal-dependent Pre-mRNA splicing in anucleate platelets [J].
Denis, MM ;
Tolley, ND ;
Bunting, M ;
Schwertz, H ;
Jiang, HM ;
Lindemann, S ;
Yost, CC ;
Rubner, FJ ;
Albertine, KH ;
Swoboda, KJ ;
Fratto, CM ;
Tolley, E ;
Kraiss, LW ;
McIntyre, TM ;
Zimmerman, GA ;
Weyrich, AS .
CELL, 2005, 122 (03) :379-391
[10]
De novo synthesis of cyclooxygenase-1 counteracts the suppression of platelet thromboxane biosynthesis by aspirin [J].
Evangelista, V ;
Manarini, S ;
Di Santo, A ;
Capone, ML ;
Ricciotti, E ;
Di Francesco, L ;
Tacconelli, S ;
Sacchetti, A ;
D'Angelo, S ;
Scilimati, A ;
Sciulli, MG ;
Patrignani, P .
CIRCULATION RESEARCH, 2006, 98 (05) :593-595