首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Monocyte tissue factor response is decreased in patients with hyperlipidemia.
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Monocyte tissue factor response is decreased in patients with hyperlipidemia.

机译:高脂血症患者单核细胞组织因子反应降低。

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摘要

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<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.
机译:单核细胞是通过刺激时组织因子(TF)的表达和组织因子途径抑制剂(TFPI)(一种TF途径的选择性抑制剂)的表达而对凝血的有效调节剂。由于高脂血症可以改变某些单核细胞功能,因此我们比较了65名健康降血脂正常对照组和38名未经治疗的高血脂患者之间循环单核细胞的TF和TFPI表达以及血浆TFPI水平。还检查了TF和TFPI与血浆脂蛋白的关系。在通过密度梯度离心从血液中分离后以及在有或没有脂多糖(LPS)的情况下短暂培养后,评估外周单个核细胞中的TF和TFPI表达。 TF和TFPI活性以及抗原分别使用酰胺水解测定法和酶联免疫吸附测定法在单核细胞裂解物中进行测定。使用相同的方法在血浆中测量TFPI活性和抗原。还测定了血浆因子VII(FVII)的活性和抗原。高脂血症患者的LPS刺激的单核细胞TF活性和抗原低于对照组(0.0001 <0.03)。高脂血症患者单核细胞TF表达的减少与单核细胞TFPI的增加无关。单核细胞TF活性与动脉粥样硬化成分呈负相关,与保护成分呈正相关,特别是在离体LPS刺激后。与对照组相比,高脂血症患者的TFPI和FVII血浆水平升高。这些结果表明,来自高脂血症受试者的单核细胞循环产生的TF产生损伤,这与动脉粥样硬化性脂蛋白组分的增加有关。需要进一步的研究来阐明这种抑制的机理。

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