George F, Brisson C, Poncelet P, Laurent J C, Massot O, Arnoux D, Ambrosi P, Klein-Soyer C, Cazenave J P, Sampol J
Laboratoire d'Hématologie, Faculté de Pharmacie, Marseille, France.
Thromb Haemost. 1992 Jan 23;67(1):147-53.
The presence in whole blood of circulating endothelial cells (EC) has been a subject of debate for many years. It could represent a good marker of vessel injury. We demonstrate here that human endothelial cells can be directly isolated and identified in circulating blood by means of an endothelial cell specific monoclonal antibody, S-Endo1, coupled to micromagnetic beads. The specificity and efficacy of the assay were established using normal blood samples with cultured EC added. Specific rosettes formed between EC and beads could subsequently be isolated with a magnet. The rosetted cells were recovered with a yield greater than 80%. Their endothelial origin was confirmed by the positive labelling of von Willebrand factor and thrombomodulin, as well as the presence of Weibel-Palade bodies. We applied this method to demonstrate significantly increased levels of EC in venous and arterial human blood samples in patients undergoing heart catheterization. This new whole blood immuno-separation method may be useful in determining endothelial cell injury in vascular disorders.
循环内皮细胞(EC)在全血中的存在多年来一直是一个有争议的话题。它可能是血管损伤的一个良好标志物。我们在此证明,通过与微磁珠偶联的内皮细胞特异性单克隆抗体S-Endo1,可以在循环血液中直接分离和鉴定人内皮细胞。使用添加了培养的内皮细胞的正常血液样本确定了该检测方法的特异性和有效性。内皮细胞与磁珠之间形成的特异性玫瑰花结随后可用磁铁分离。回收的玫瑰花结细胞产率大于80%。通过血管性血友病因子和血栓调节蛋白的阳性标记以及魏尔-帕拉德小体的存在,证实了它们的内皮来源。我们应用该方法证明,在接受心脏导管插入术的患者的静脉和动脉血样本中,内皮细胞水平显著升高。这种新的全血免疫分离方法可能有助于确定血管疾病中的内皮细胞损伤。