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乙二胺四乙酸(EDTA)和柠檬酸盐对补体第一成分C1及其C1q亚成分功能活性的影响。

Effect of EDTA and citrate on the functional activity of the first component of complement, C1, and the C1q subcomponent.

作者信息

Zapf S, Loos M

出版信息

Immunobiology. 1985 Sep;170(3):123-32. doi: 10.1016/S0171-2985(85)80085-1.

Abstract

The first component of complement, C1, is a calcium-dependent complex of the three distinct subcomponents, C1q, C1r, and C1s. Earlier observations revealed that treatment of C1 with EDTA led to a loss of hemolytic C1 activity even after recalcification. Therefore, it was of interest to study whether EDTA has an additional effect on C1 and its subcomponents, beside its chelating capacity. The chelating effect of EDTA was compared to that of citrate. It was found that treatment of C1 or C1 with EDTA followed by addition of Ca++ led to a loss of hemolytic activity up to 90%, depending on EDTA concentration. Even pretreatment of EDTA with varying amounts of Ca++ did not prevent the inactivation of C1 or C1. In contrast, after dissociation of C1 or C1 by citrate, 100% of the original C1q activity is recoverable on addition of C1q deficient serum as source of C1r and C1s. EDTA-treated serum, however, showed a concentration-dependent loss of hemolytic C1q activity, indicating an inhibitory effect of EDTA on C1q. EDTA-treated C1q, fluid phase or bound to EA, was no longer able to form an hemolytically active C1 complex by interaction with C1r and C1s.

摘要

补体的第一个成分C1是由三种不同亚成分C1q、C1r和C1s组成的钙依赖性复合物。早期观察发现,用乙二胺四乙酸(EDTA)处理C1后,即使重新加入钙离子,溶血C1活性仍会丧失。因此,研究EDTA除了其螯合能力外,是否对C1及其亚成分还有其他作用就很有意义。将EDTA的螯合作用与柠檬酸盐的螯合作用进行了比较。结果发现,用EDTA处理C1或C1后再加入钙离子,溶血活性会丧失高达90%,这取决于EDTA的浓度。即使先用不同量的钙离子预处理EDTA,也不能防止C1或C1的失活。相比之下,用柠檬酸盐使C1或C1解离后,加入缺乏C1q的血清作为C1r和C1s的来源,可恢复100%的原始C1q活性。然而,经EDTA处理的血清显示溶血C1q活性呈浓度依赖性丧失,表明EDTA对C1q有抑制作用。经EDTA处理的C1q,无论是液相还是与致敏红细胞(EA)结合,都不再能够通过与C1r和C1s相互作用形成具有溶血活性的C1复合物。

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