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C1 灭活剂与因子 VII 的冷促进激活

C-1 inactivator and cold-promoted activation of factor VII.

作者信息

van Royen E A, Lohman S, Voss M, Pondman K W

出版信息

J Lab Clin Med. 1978 Aug;92(2):152-63.

PMID:681808
Abstract

When exposed to temperatures between -5 degree and +5 degree C, plasma from pregnant women and from certain blood donors show shortening of the Thrombotest clotting time, kallikrein formation, and activation of blood-clotting factor VII. This phenomenon has been called cold-promoted activation of factor VII (CPA). In this study, it was found that CPA-positive plasma or serum samples which had been exposed to low temepratures showed spontaneous disappearance of C-1-inactivator activity in parallel to the shortening of the Thrombotest clotting time. C-1-inactivator antigen was not affected by storage at 4 degree C. In these CPA-possitive samples the loss of C-1-inactivator activity is caused partially by the formation of kallikrein at this temperature because when kallikrelin was added to C-1 inactivator, the latter was inactive when tested in the esterolytic assay. The formation of Hageman factor fragments may add to further loss. Purified C-1 inactivator effectively inhibited the CPA phenomenon, whereas alpha2-macroglobulin did so only weakly. This finding indicates that during exposure of CPA-positive plasma samples to low temperatures, Hageman factor fragments, which are inhibited only by C-1 inactivator, induce the activation of the kallikrein system and blood clotting factor VII. The reported lowered activity of C-1 inactivator in pregnancy is probably an artifact caused by generation of CPA during storage, since in fresh samples the levels were compeletely normal. Similarly, various subjects classified as belonging to the variant type of HANE (low C-1-inactivator activity with a normal antigen content) were found to have normal C-1-inactivator activity when determinations were made on fresh instead of frozen samples. It is recommended that plasma or serum samples should not be exposed to temperatures between -5degree and +5degree C prior to the determination of C-1-inactivator activity. Moreover, during purification procedures of kallikrein-binding antiproteases such as C-1 inactivator and also alpha2-macroglobulin, the occurrence of CPA should be avoided by the use of CPA-negative plasma as starting material.

摘要

当暴露于-5摄氏度至+5摄氏度之间的温度时,孕妇和某些献血者的血浆会出现凝血酶检测凝血时间缩短、激肽释放酶形成以及凝血因子VII激活的现象。这种现象被称为因子VII的冷促进激活(CPA)。在本研究中,发现暴露于低温的CPA阳性血浆或血清样本显示C-1灭活剂活性自发消失,同时凝血酶检测凝血时间缩短。C-1灭活剂抗原不受4摄氏度储存的影响。在这些CPA阳性样本中,C-1灭活剂活性的丧失部分是由于在此温度下激肽释放酶的形成,因为当将激肽释放酶添加到C-1灭活剂中时,后者在酯解测定中无活性。Hageman因子片段的形成可能会进一步导致活性丧失。纯化的C-1灭活剂有效地抑制了CPA现象,而α2-巨球蛋白的抑制作用较弱。这一发现表明,在CPA阳性血浆样本暴露于低温期间,仅被C-1灭活剂抑制的Hageman因子片段会诱导激肽释放酶系统和凝血因子VII的激活。报道的孕期C-1灭活剂活性降低可能是储存期间CPA产生导致的假象,因为新鲜样本中的水平完全正常。同样,当对新鲜而非冷冻样本进行测定时,发现各种被归类为遗传性血管性水肿变异型(C-1灭活剂活性低但抗原含量正常)的受试者具有正常的C-1灭活剂活性。建议在测定C-1灭活剂活性之前,血浆或血清样本不应暴露于-5摄氏度至+5摄氏度之间的温度。此外,在诸如C-1灭活剂以及α2-巨球蛋白等激肽释放酶结合抗蛋白酶的纯化过程中,应使用CPA阴性血浆作为起始材料以避免CPA的发生。

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