Ghevaert Cedric, Salsmann Alexandre, Watkins Nicholas A, Schaffner-Reckinger Elisabeth, Rankin Angela, Garner Stephen F, Stephens Jonathan, Smith Graham A, Debili Najet, Vainchenker William, de Groot Philip G, Huntington James A, Laffan Mike, Kieffer Nelly, Ouwehand Willem H
Department of Haematology, University of Cambridge, UK.
Blood. 2008 Apr 1;111(7):3407-14. doi: 10.1182/blood-2007-09-112615. Epub 2007 Dec 7.
We report a 3-generation pedigree with 5 individuals affected with a dominantly inherited macrothrombocytopenia. All 5 carry 2 nonsynonymous mutations resulting in a D723H mutation in the beta3 integrin and a P53L mutation in glycoprotein (GP) Ibalpha. We show that GPIbalpha-L53 is phenotypically silent, being also present in 3 unaffected pedigree members and in 7 of 1639 healthy controls. The beta3-H723 causes constitutive, albeit partial, activation of the alphaIIbbeta3 complex by disruption of the highly conserved cytoplasmic salt bridge with arginine 995 in the alphaIIb integrin as evidenced by increased PAC-1 but not fibrinogen binding to the patients' resting platelets. This was confirmed in CHO alphaIIbbeta3-H723 transfectants, which also exhibited increased PAC-1 binding, increased adhesion to von Willebrand factor (VWF) in static conditions and to fibrinogen under shear stress. Crucially, we show that in the presence of fibrinogen, alphaIIbbeta3-H723, but not wild-type alphaIIbbeta3, generates a signal that leads to the formation of proplatelet-like protrusions in transfected CHO cells. Abnormal proplatelet formation was confirmed in the propositus's CD34+ stem cell-derived megakaryocytes. We conclude that the constitutive activation of the alphaIIbbeta3-H723 receptor causes abnormal proplatelet formation, leading to incorrect sizing of platelets and the thrombocytopenia observed in the pedigree.
我们报告了一个三代家系,其中5名个体患有显性遗传的大血小板减少症。所有5名患者均携带2个非同义突变,导致β3整合素发生D723H突变,糖蛋白(GP)Ibalpha发生P53L突变。我们发现GPIbalpha-L53在表型上是沉默的,在3名未受影响的家系成员以及1639名健康对照中的7人中也存在。β3-H723通过破坏αIIb整合素中与精氨酸995高度保守的细胞质盐桥,导致αIIbbeta3复合物组成性(尽管是部分)激活,这可通过PAC-1结合增加得以证明,但纤维蛋白原与患者静息血小板的结合并未增加。这在CHO αIIbbeta3-H723转染细胞中得到证实,这些细胞还表现出PAC-1结合增加、在静态条件下对血管性血友病因子(VWF)的黏附增加以及在剪切应力下对纤维蛋白原的黏附增加。至关重要的是,我们表明在存在纤维蛋白原的情况下,αIIbbeta3-H723而非野生型αIIbbeta3会产生一个信号,导致转染的CHO细胞中形成前血小板样突起。在先证者的CD34 +干细胞衍生的巨核细胞中证实了异常的前血小板形成。我们得出结论,αIIbbeta3-H723受体的组成性激活导致异常的前血小板形成,从而导致血小板大小异常以及在家系中观察到的血小板减少症。