Tandon N N, Rock G, Jamieson G A
Cell Biology Department, American Red Cross, Rockville, Maryland 20855.
Br J Haematol. 1994 Dec;88(4):816-25. doi: 10.1111/j.1365-2141.1994.tb05122.x.
The membrane glycoprotein CD36 (GPIV, M(r) 88,000) is found on platelets, monocytes and endothelial cells of the microvasculature. In the present study, anti CD36 antibodies have been identified as occurring with high frequency in patients with thrombotic thrombocytopenic purpura. The presence of anti CD36 antibodies in 15 TTP plasma samples thought to contain them on the basis of an initial screening by protein blots was confirmed by re-screening against a standard of purified CD36, by immunoprecipitation from 125I-labelled control platelets and by dot blots against purified CD36. In a further 28 random samples examined, 23/27 (85%) were CD36-positive by immunoprecipitation, 21/28 (75%) by protein blotting, and 17/28 (60%) by dot blots against purified CD36. On protein blots following SDS-PAGE, immunoprecipitates produced from normal platelets by TTP plasma gave positive reactions with the anti CD36 monoclonal antibody 125I-Mo91. One half of the total TTP samples examined (21/42) caused approximately 70% release in control platelets loaded with 14C-serotonin. Of samples causing release > or = 70%, one-half (8/15) failed to cause release from Naka-negative platelets which constitutively lack CD36 showing that CD36 was the sole target for platelet activation in these TTP samples. These studies demonstrate that antibodies directed against CD36 occur frequently in TTP patients and could cause thrombotic complications and vascular damage by reacting with the parent antigen present in platelets and endothelial cells.
膜糖蛋白CD36(GPIV,分子量88,000)存在于血小板、单核细胞以及微脉管系统的内皮细胞上。在本研究中,抗CD36抗体在血栓性血小板减少性紫癜患者中被发现具有高频率出现的情况。通过针对纯化CD36标准品的重新筛选、从125I标记的对照血小板中进行免疫沉淀以及针对纯化CD36的斑点印迹法,证实了在15份经蛋白印迹初步筛选认为含有抗CD36抗体的血栓性血小板减少性紫癜血浆样本中存在该抗体。在另外检测的28份随机样本中,通过免疫沉淀法23/27(85%)为CD36阳性,通过蛋白印迹法21/28(75%)为阳性,通过针对纯化CD36的斑点印迹法17/28(60%)为阳性。在SDS - PAGE后的蛋白印迹上,血栓性血小板减少性紫癜血浆从正常血小板产生的免疫沉淀物与抗CD36单克隆抗体125I - Mo91发生阳性反应。所检测的血栓性血小板减少性紫癜样本中有一半(21/42)导致加载了14C - 5羟色胺的对照血小板释放约70%。在导致释放≥70%的样本中,有一半(8/15)未能使组成性缺乏CD36的中阴性血小板释放,这表明在这些血栓性血小板减少性紫癜样本中CD36是血小板激活的唯一靶点。这些研究表明,针对CD36的抗体在血栓性血小板减少性紫癜患者中频繁出现,并可能通过与血小板和内皮细胞中存在的亲本抗原反应而导致血栓形成并发症和血管损伤。