de Sousa J C, Soria C, Ayrault-Jarrier M, Pastier D, Bruckert E, Amiral J, Bereziat G, Caen J P
Hôpital Lariboisière, Service d'hématologie, Paris.
J Clin Pathol. 1988 Sep;41(9):940-4. doi: 10.1136/jcp.41.9.940.
The association between the concentration of different plasma lipoproteins and plasma factor VII (F VII) was analysed by isolating plasma very low density lipoprotein (VLDL), low density lipoprotein (LDL), and high density lipoprotein (HDL) lipoproteins and assessing their in vitro interaction with F VII by immunoenzyme assay using peroxidase labelled anti-factor VII immunoglobulins to determine whether F VII coagulant activity is prognostic for cardiovascular mortality. F VII bound to triglyceride rich lipoproteins, the fixation being stronger on chylomicrons and VLDL fractions than on LDL fractions. In our experiments HDL did not bind to F VII. The fixation of coagulation factor X (FX) tested by the same method is comparable with that of F VII. The nature of this fixation seemed to arise from hydrophobic interaction as calcium was not necessary and the use of Tween 20 inhibited the interaction. The binding of factors VII and X was increased when lipids were previously treated by phospholipase C and the interaction seemed to be completely dependent on the lipid part of the lipoproteins. Hyrophobic fixation is a possible mechanism of interaction of plasma lipoproteins and F VII and X, and it may be of importance in the covariance of triglyceride concentrations and the activity of vitamin K dependent coagulation factors.
通过分离血浆极低密度脂蛋白(VLDL)、低密度脂蛋白(LDL)和高密度脂蛋白(HDL),并使用过氧化物酶标记的抗因子VII免疫球蛋白通过免疫酶测定法评估它们与因子VII的体外相互作用,分析不同血浆脂蛋白浓度与血浆因子VII(F VII)之间的关联,以确定F VII凝血活性是否可预测心血管死亡率。F VII与富含甘油三酯的脂蛋白结合,在乳糜微粒和VLDL组分上的结合比在LDL组分上更强。在我们的实验中,HDL不与F VII结合。用相同方法检测的凝血因子X(FX)的结合与F VII相当。这种结合的性质似乎源于疏水相互作用,因为钙不是必需的,并且使用吐温20会抑制这种相互作用。当脂质预先用磷脂酶C处理时,因子VII和X的结合增加,并且这种相互作用似乎完全依赖于脂蛋白的脂质部分。疏水结合是血浆脂蛋白与F VII和X相互作用的一种可能机制,并且它可能在甘油三酯浓度与维生素K依赖性凝血因子活性的协方差中起重要作用。