Chabannes B, Molière P, Pacheco Y, Lagarde M
INSERM U 352, Chimie Biologique INSA-Lyon, Villeurbanne, France.
Biochem J. 1994 Jun 15;300 ( Pt 3)(Pt 3):685-91. doi: 10.1042/bj3000685.
The amount of the 12-lipoxygenase and cyclo-oxygenase products, 12(S)-hydroxy-(Z,Z,E,Z)-5,8,10,14-eicosatetraenoic acid (12-HETE) and 12(S)-hydroxy-(E,E,Z)-5,8,10-heptadecatrienoic acid (HHT), in human platelets stimulated by thrombin (0.1 and 2.5 units/ml), was studied in the presence of autologous neutrophils. A decreased formation of both products was induced by unstimulated neutrophils or neutrophils challenged with N-formylmethionyl- leucyl-phenylalanine (0.1 microM) or Ca2+ ionophore A23187 (0.15 microM). The effect of neutrophils was observed only in the presence of Ca2+. 12-HETE and HHT were also produced in platelets stimulated with thrombin in the absence of Ca2+ and/or Mg2+, but their level was not altered by neutrophils. 12(S),20-Dihydroxy-(Z,Z,E,Z)-5,8,10,14-eicosatetraenoic acid (12,20-DHETE), the cytochrome P-450 product from 12-HETE in neutrophils, was hardly detected, and its level did not compensate for the decrease in 12-HETE observed after platelet and neutrophil co-incubation. 5(S),12(S)-Dihydroxy-(E,Z,E,Z)- 6,8,10,14-eicosatetraenoic acid (5(S),12(S)-DHETE), the 5-lipoxygenase product of 12-HETE in neutrophils, was never detectable. In addition, the inhibition of 12-HETE and HHT formations appeared not to be due to degradation or thrombin uptake by neutrophils, nor was the decrease observed when the two cell populations were physically separated. A monoclonal antibody against the human platelet glycoprotein GMP140 (CD62), mediating Ca(2+)-dependent platelet-neutrophil adhesion, mimicked the inhibitory effect of neutrophils in a dose-dependent fashion. Furthermore, the 12-HETE and HHT productions were not affected when platelets were stimulated in the presence of neutrophils previously incubated with sialidase, which removes the sialic acid from a sialyl Lewis(x) structure assumed to be the neutrophil receptor for platelet GMP140. We conclude that the decrease in thrombin-stimulated 12-HETE and HHT formation observed when platelets were co-incubated with autologous neutrophils might be the consequence of platelet-neutrophil adherence, presumably through platelet GMP140.
在自体中性粒细胞存在的情况下,研究了凝血酶(0.1和2.5单位/毫升)刺激的人血小板中12 - 脂氧合酶和环氧化酶产物,即12(S)-羟基-(Z,Z,E,Z)-5,8,10,14-二十碳四烯酸(12-HETE)和12(S)-羟基-(E,E,Z)-5,8,10-十七碳三烯酸(HHT)的生成量。未刺激的中性粒细胞或用N-甲酰甲硫氨酰-亮氨酰-苯丙氨酸(0.1微摩尔)或钙离子载体A23187(0.15微摩尔)刺激的中性粒细胞可诱导这两种产物生成减少。仅在有钙离子存在时才观察到中性粒细胞的这种作用。在无钙离子和/或镁离子的情况下,凝血酶刺激的血小板也会产生12-HETE和HHT,但中性粒细胞不会改变它们的水平。几乎检测不到中性粒细胞中12-HETE经细胞色素P-450生成的产物12(S),20-二羟基-(Z,Z,E,Z)-5,8,10,14-二十碳四烯酸(12,20-DHETE),其水平也无法弥补血小板与中性粒细胞共同孵育后观察到的12-HETE的减少。从未检测到中性粒细胞中12-HETE经5-脂氧合酶生成的产物5(S),12(S)-二羟基-(E,Z,E,Z)-6,8,10,14-二十碳四烯酸(5(S),12(S)-DHETE)。此外,12-HETE和HHT生成的抑制似乎并非由于中性粒细胞对其降解或摄取凝血酶,当两个细胞群体物理分离时也未观察到减少。一种针对人血小板糖蛋白GMP140(CD62)的单克隆抗体,介导钙离子依赖性血小板-中性粒细胞黏附,以剂量依赖方式模拟了中性粒细胞的抑制作用。此外,当血小板在先前用唾液酸酶孵育过的中性粒细胞存在下受到刺激时,12-HETE和HHT的生成不受影响,唾液酸酶可从假定为血小板GMP140的中性粒细胞受体的唾液酸化路易斯(x)结构上去除唾液酸。我们得出结论,血小板与自体中性粒细胞共同孵育时观察到的凝血酶刺激的12-HETE和HHT生成减少可能是血小板-中性粒细胞黏附的结果,大概是通过血小板GMP140介导的。