Skinner M P, Lucas C M, Burns G F, Chesterman C N, Berndt M C
Department of Medicine, University of Sydney, Westmead Hospital, N.S.W., Australia.
J Biol Chem. 1991 Mar 25;266(9):5371-4.
GMP-140 is a 140-kDa granule membrane glycoprotein localized to the alpha-granules of platelets and the Weibel-Palade bodies of endothelial cells. Expression of GMP-140 on the activated cell surface has been shown to mediate the adhesion of thrombin-activated platelets to neutrophils and monocytes and the transient adhesion of neutrophils to endothelium. In contrast, fluid-phase GMP-140 strongly inhibits the CD18-dependent adhesion of tumor necrosis factor alpha-activated neutrophils to endothelium suggesting that GMP-140 can also serve an anti-adhesive function. In the present report, it is demonstrated that fluid-phase GMP-140 which exists predominantly as a tetramer binds to a single class of high affinity receptor on neutrophils and HL60 cells. Binding of 125I-labeled GMP-140 to neutrophils and HL60 cells and the rosetting of neutrophils and HL60 cells by thrombin-activated platelets were inhibited by EDTA, excess unlabeled fluid-phase GMP-140, Fab fragments of an affinity-purified rabbit anti-GMP-140 antibody, and by the murine anti-GMP-140 monoclonal antibody, AK 4. Both neutrophil and HL60 GMP-140 binding and platelet rosetting were strongly inhibited by heparin, fucoidin, and dextran sulfate 500,000, were partially inhibited by dextran sulfate 5,000 and lambda- and kappa-carrageenan, but were not inhibited by chondroitins 4- and 6-sulfate. Since this sulfated glycan specificity is identical to that previously reported by us for GMP-140, the present results suggest that the sulfated glycan binding site and the neutrophil receptor binding site on GMP-140 are either identical or proximal.
GMP - 140是一种140千道尔顿的颗粒膜糖蛋白,定位于血小板的α颗粒和内皮细胞的魏尔-帕拉德小体。已表明,活化细胞表面的GMP - 140表达介导凝血酶激活的血小板与中性粒细胞和单核细胞的黏附,以及中性粒细胞与内皮的短暂黏附。相比之下,液相GMP - 140强烈抑制肿瘤坏死因子α激活的中性粒细胞与内皮的CD18依赖性黏附,这表明GMP - 140也可发挥抗黏附功能。在本报告中,证明主要以四聚体形式存在的液相GMP - 140与中性粒细胞和HL60细胞上的一类高亲和力受体结合。125I标记的GMP - 140与中性粒细胞和HL60细胞的结合以及凝血酶激活的血小板对中性粒细胞和HL60细胞的花环形成受到EDTA、过量未标记的液相GMP - 140、亲和纯化的兔抗GMP - 140抗体的Fab片段以及鼠抗GMP - 140单克隆抗体AK 4的抑制。肝素、岩藻依聚糖和500,000硫酸葡聚糖强烈抑制中性粒细胞和HL60细胞的GMP - 140结合以及血小板花环形成,5,000硫酸葡聚糖以及λ - 和κ - 角叉菜胶部分抑制,而4 - 和6 - 硫酸软骨素则无抑制作用。由于这种硫酸化聚糖特异性与我们之前报道的GMP - 140的特异性相同,目前的结果表明,GMP - 140上的硫酸化聚糖结合位点和中性粒细胞受体结合位点要么相同,要么相邻。