Rugeri L, Susen S, Bard J M, Corseaux D, Gavériaux V, Devos P, Lecerf J M, Duriez P, Jude B
Laboratoire d'Hématologie, Centre Hospitalier Régional Universitaire and Institut Pasteur Lille, France.
Thromb Res. 1999 Nov 15;96(4):283-92. doi: 10.1016/s0049-3848(99)00112-7.
Monocytes are potent regulators of blood coagulation through the expression of tissue factor (TF) on stimulation and of tissue factor pathway inhibitor (TFPI), a selective inhibitor of TF pathway. As hyperlipidemia can modify some monocyte functions, we compared the TF and TFPI expression by circulating monocytes and the plasma TFPI levels between 65 healthy normolipemic controls and 38 nontreated hyperlipemic patients. TF and TFPI relationships with plasma lipoproteins are also examined. TF and TFPI expression were evaluated in peripheral mononuclear cells after isolation from blood by density gradient centrifugation and after short culture with or without lipopolysaccharide (LPS). TF and TFPI activity and antigen were measured in mononuclear cell lysates using amidolytic assay and enzyme-linked immunosorbent assay, respectively. TFPI activity and antigen were measured in plasma using the same methods. Plasma factor VII (FVII) activity and antigen were also determined. LPS-stimulated monocyte TF activity and antigen were lower in hyperlipidemic patients than in controls (0.0001<p<0.03). This decrease of monocyte TF expression in hyperlipidemic patients was not related to an increase of monocyte TFPI. Monocyte TF activity was negatively correlated to atherogenic fractions and positively correlated to protective fractions, specially after ex vivo LPS stimulation. Increased TFPI and FVII plasma levels were found in hyperlipidemic patients compared to controls. These results indicate an impairment of TF production by circulating monocytes from hyperlipidemic subjects, which is linked to the increase of atherogenic lipoprotein fractions. Further studies are required to elucidate the mechanism of this inhibition.
单核细胞是血液凝固的有效调节因子,通过在刺激时表达组织因子(TF)以及组织因子途径抑制剂(TFPI,TF途径的选择性抑制剂)来发挥作用。由于高脂血症可改变单核细胞的某些功能,我们比较了65名健康血脂正常对照者和38名未经治疗的高脂血症患者循环单核细胞中TF和TFPI的表达以及血浆TFPI水平。还研究了TF和TFPI与血浆脂蛋白的关系。通过密度梯度离心从血液中分离外周单核细胞后,以及在有或无脂多糖(LPS)的情况下短期培养后,评估TF和TFPI的表达。分别使用酰胺分解测定法和酶联免疫吸附测定法测量单核细胞裂解物中的TF和TFPI活性及抗原。使用相同方法测量血浆中的TFPI活性和抗原。还测定了血浆因子VII(FVII)活性和抗原。高脂血症患者中LPS刺激的单核细胞TF活性和抗原低于对照组(0.0001 < p < 0.03)。高脂血症患者单核细胞TF表达的这种降低与单核细胞TFPI的增加无关。单核细胞TF活性与致动脉粥样硬化组分呈负相关,与保护性组分呈正相关,特别是在体外LPS刺激后。与对照组相比,高脂血症患者血浆中TFPI和FVII水平升高。这些结果表明高脂血症患者循环单核细胞中TF产生受损,这与致动脉粥样硬化脂蛋白组分的增加有关。需要进一步研究以阐明这种抑制的机制。