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健康供体血浆中存在尿激酶型纤溶酶原激活剂受体,阵发性夜间血红蛋白尿患者血浆中该受体水平升高。

The receptor for urokinase plasminogen activator is present in plasma from healthy donors and elevated in patients with paroxysmal nocturnal haemoglobinuria.

作者信息

Rønne E, Pappot H, Grøndahl-Hansen J, Høyer-Hansen G, Plesner T, Hansen N E, Danø K

机构信息

Finsen Laboratory, Rigshospitalet, Copenhagen, Denmark.

出版信息

Br J Haematol. 1995 Mar;89(3):576-81. doi: 10.1111/j.1365-2141.1995.tb08366.x.

Abstract

The urokinase plasminogen activator (uPA) is a proteolytic enzyme which converts the proenzyme plasminogen to the active serine protease plasmin. A cell surface receptor for uPA (uPAR) is attached to the cell membrane by a glycosyl-phosphatidylinositol anchor. Binding of uPA to uPAR leads to an enhanced plasmin formation and thereby an amplification of pericellular proteolysis. We have shown previously that uPAR is expressed on normal blood monocytes and granulocytes, but is deficient on affected blood monocytes and granulocytes in patients with paroxysmal nocturnal haemoglobinuria (PNH), and that uPAR is present in plasma from these patients. In this study a newly established sensitive enzyme-linked immunosorbent assay (ELISA) has been applied for quantitation of uPAR in plasma. Unexpectedly, we found that uPAR is not only present in PNH plasma but also in plasma from healthy individuals. In 39 healthy individuals the mean plasma-uPAR value +/- SD was 31 +/- 15 pM, median 28 (range 11-108), and the corresponding value for six PNH patients was 116 +/- 67 pM, median 90 (range 61-228). The elevated uPAR-level in PNH patients was highly significant (Mann-Whitney test; P < 0.0001), and may possibly contribute to the propensity for thrombosis in PNH by inhibition of the fibrinolytic system. Binding of pro-uPA by uPAR in plasma may interfere with the appropriate binding of pro-uPA to cell-bound uPAR and therefore inhibit cell-associated plasmin generation and fibrinolysis. It is likely that the uPAR in normal plasma reflects the overall level of activity of the uPAR-mediated cell surface proteolysis. The present ELISA may be used for studies of uPAR levels in plasma from patients with conditions in which this activity might be increased, such as cancer and inflammatory disorders. Future studies will determine if uPAR in plasma is a parameter of clinical importance in these diseases.

摘要

尿激酶型纤溶酶原激活剂(uPA)是一种蛋白水解酶,可将纤溶酶原前体转化为活性丝氨酸蛋白酶纤溶酶。uPA的细胞表面受体(uPAR)通过糖基磷脂酰肌醇锚定附着于细胞膜。uPA与uPAR结合会导致纤溶酶生成增加,从而放大细胞周围的蛋白水解作用。我们之前已经表明,uPAR在正常血液单核细胞和粒细胞上表达,但阵发性夜间血红蛋白尿(PNH)患者受影响的血液单核细胞和粒细胞上缺乏uPAR,且这些患者的血浆中存在uPAR。在本研究中,一种新建立的灵敏酶联免疫吸附测定(ELISA)已用于定量血浆中的uPAR。出乎意料的是,我们发现uPAR不仅存在于PNH患者的血浆中,也存在于健康个体的血浆中。在39名健康个体中,血浆uPAR的平均值±标准差为31±15 pM,中位数为28(范围11 - 108),6名PNH患者的相应值为116±67 pM,中位数为90(范围61 - 228)。PNH患者中uPAR水平升高具有高度显著性(曼-惠特尼检验;P < 0.0001),并且可能通过抑制纤溶系统而导致PNH患者的血栓形成倾向。血浆中的uPAR与pro - uPA结合可能会干扰pro - uPA与细胞结合的uPAR的正常结合,从而抑制细胞相关的纤溶酶生成和纤维蛋白溶解。正常血浆中的uPAR可能反映了uPAR介导的细胞表面蛋白水解的总体活性水平。目前的ELISA可用于研究该活性可能增加的疾病患者血浆中的uPAR水平,如癌症和炎症性疾病。未来的研究将确定血浆中的uPAR是否是这些疾病中具有临床重要性的参数。

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