Impaired thrombin generation in β2-glycoprotein I null mice

被引:69
作者
Sheng, YH
Reddel, SW
Herzog, H
Wang, YX
Brighton, T
France, MP
Robertson, SA
Krilis, SA
机构
[1] Univ New S Wales, Dept Immunol Allergy & Infect Dis, St George Hosp, Kogarah, NSW 2217, Australia
[2] Univ New S Wales, Dept Med, St George Hosp, Kogarah, NSW 2217, Australia
[3] Univ New S Wales, Dept Haematol, St George Hosp, Kogarah, NSW 2217, Australia
[4] St Vincents Hosp, Garvan Inst Med Res, Darlinghurst, NSW 2010, Australia
[5] Univ Sydney, Dept Vet Anat & Pathol, Sydney, NSW 2006, Australia
[6] Univ Adelaide, Dept Obstet & Gynaecol, Adelaide, SA 5005, Australia
[7] Univ Adelaide, Reprod Med Unit, Adelaide, SA 5005, Australia
关键词
D O I
10.1074/jbc.M010990200
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
Autoimmune antibodies to beta (2)-glycoprotein I (beta 2GPI) have been proposed to be clinically relevant because of their strong association with thrombosis, miscarriage, and thrombocytopenia, By using a homologous recombination approach, beta 2GPI-null mice were generated to begin to understand the physiologic and pathologic role of this prominent plasma protein in mammals. When beta 2GPI heterozygotes on a 129/Sv/C57BL/6 mixed genetic background were intercrossed, only 8.9% of the resulting 336 offspring possessed both disrupted alleles, These data suggest that beta 2GPI plays a beneficial role in implantation and/or fetal development in at least some mouse strains. Although those beta 2GPI-null mice that were born appeared to be relatively normal anatomically and histologically, subsequent analysis revealed that they possessed an impaired in vitro ability to generate thrombin relative to wild type mice. Thus, beta 2GPI also appears to play an important role in thrombin-mediated coagulation.
引用
收藏
页码:13817 / 13821
页数:5
相关论文
共 20 条
[1]   Characterization of phosphatidylserine-dependent β2-glycoprotein I macrophage interactions -: Implications for apoptotic cell clearance by phagocytes [J].
Balasubramanian, K ;
Schroit, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (44) :29272-29277
[2]  
BANCSI LFJMM, 1992, THROMB HAEMOSTASIS, V67, P649
[3]  
Del Papa N, 1998, J IMMUNOL, V160, P5572
[4]   SENSITIVE TEST DEMONSTRATING LUPUS ANTICOAGULANT AND ITS BEHAVIORAL PATTERNS [J].
EXNER, T ;
RICKARD, KA ;
KRONENBERG, H .
BRITISH JOURNAL OF HAEMATOLOGY, 1978, 40 (01) :143-151
[5]  
GINSBERG JS, 1993, BLOOD, V81, P2958
[6]  
HANLY JG, 1998, LUPUS, V7, P219
[7]   CHARACTERIZATION OF PLASMA-LIPIDS AND LIPOPROTEINS IN PATIENTS WITH BETA-2-GLYCOPROTEIN-I (APOLIPOPROTEIN-H) DEFICIENCY [J].
HOEG, JM ;
SEGAL, P ;
GREGG, RE ;
CHANG, YS ;
LINDGREN, FT ;
ADAMSON, GL ;
FRANK, M ;
BRICKMAN, C ;
BREWER, HB .
ATHEROSCLEROSIS, 1985, 55 (01) :25-34
[8]   Current insights into the "antiphospholipid" syndrome: Clinical, immunological, and molecular aspects [J].
Kandiah, DA ;
Sali, A ;
Sheng, YH ;
Victoria, EJ ;
Marquis, DM ;
Coutts, SM ;
Krilis, SA .
ADVANCES IN IMMUNOLOGY, VOL 70, 1998, 70 :507-563
[9]  
KONTGEN F, 1993, METHOD ENZYMOL, V225, P878
[10]   High affinity binding of β2-glycoprotein I to human endothelial cells is mediated by annexin II [J].
Ma, KY ;
Simantov, R ;
Zhang, JC ;
Silverstein, R ;
Hajjar, KA ;
McCrae, KR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (20) :15541-15548