Deguchi Hiroshi, Banerjee Yajnavalka, Elias Darlene J, Griffin John H
Department of Molecular and Experimental Medicine, The Scripps Research Institute.
J Atheroscler Thromb. 2016 Oct 1;23(10):1159-1167. doi: 10.5551/jat.32201. Epub 2016 May 9.
Cholesteryl ester transfer protein (CETP) is an important lipid transfer factor in plasma that enhances prothrombinase activity in purified systems. This study was conducted to test the association of plasma CETP activity with venous thrombosis (VTE) and to address the procoagulant mechanism of CETP activity in prothrombinase assays.
We measured CETP lipid transfer activity in plasmas of 49 male VTE patients and in plasmas of matched controls. CETP procoagulant activity was tested in purified prothrombinase systems.
CETP lipid transfer activity levels were significantly higher in VTE patients than in controls (p=0.0008). A subset of patients carrying the CETP mutations Ala373Pro and Arg451Gln, which were also linked to the VTE risk, showed significantly higher plasma CETP activity than the noncarriers. The plasma CETP activity negatively correlated with APTT, suggesting that the CETP activity is associated with plasma coagulability. Recombinant (r) CETP bound to both factor Xa (Kd=15 nM) and Gla-domainless factor Xa (Kd=59 nM), whereas rCETP enhanced prothrombin activation by factor Xa, but not by Gla-domainless factor Xa. rCETP also required factor Va for enhancement of prothrombinase activity. When we addressed the effects of mutations in CETP on prothrombinase activity, Gln451-rCETP was found to have five-fold higher thrombin generation activity than wt-rCETP or Pro373-rCETP.
Elevated CETP lipid transfer activity in plasma was associated with the risk of VTE. Gln451-CETP, which is linked to VTE, has much higher procoagulant activity than wt-CETP. CETP might act as a physiologic procoagulant by mechanisms that involve its direct binding to factor Xa.
胆固醇酯转运蛋白(CETP)是血浆中一种重要的脂质转运因子,在纯化系统中可增强凝血酶原酶活性。本研究旨在检测血浆CETP活性与静脉血栓形成(VTE)之间的关联,并探讨在凝血酶原酶测定中CETP活性的促凝机制。
我们测定了49例男性VTE患者血浆和匹配对照组血浆中的CETP脂质转运活性。在纯化的凝血酶原酶系统中检测CETP的促凝活性。
VTE患者的CETP脂质转运活性水平显著高于对照组(p = 0.0008)。携带与VTE风险相关的CETP突变Ala373Pro和Arg451Gln的部分患者,其血浆CETP活性显著高于非携带者。血浆CETP活性与活化部分凝血活酶时间(APTT)呈负相关,提示CETP活性与血浆凝固性相关。重组(r)CETP与因子Xa(解离常数Kd = 15 nM)和无γ-羧基谷氨酸结构域的因子Xa(Kd = 59 nM)均结合,而rCETP可增强因子Xa对凝血酶原的激活作用,但不能增强无γ-羧基谷氨酸结构域的因子Xa对凝血酶原的激活作用。rCETP增强凝血酶原酶活性也需要因子Va。当我们研究CETP突变对凝血酶原酶活性的影响时,发现Gln451-rCETP的凝血酶生成活性比野生型-rCETP或Pro373-rCETP高五倍。
血浆中CETP脂质转运活性升高与VTE风险相关。与VTE相关的Gln451-CETP的促凝活性比野生型CETP高得多。CETP可能通过直接结合因子Xa的机制发挥生理性促凝作用。