Baker P J, Lint T F, McLeod B C, Behrends C L, Gewurz H
J Immunol. 1975 Feb;114(2 Pt 1):554-8.
Multiple polyanions and polycations were tested for their ability to influence formation of EC567 from C56, C7, and sheep erythrocytes. Six of 11 polyanions tested, including polyanethol sulfonate, heparin, and dextran sulfate, inhibited this reaction. By contrast, polycations (five or seven tested), including polybrene, protamine, and polyornithine, potentiated formation of EC567. The inhibition was similar to that previously described for anionic serum factors termed C567-INH, while the potentiation seemed to involve neutralization of serum C567-INH. Thus, this step of the complement attack mechanisms seems amenable to modulation by certain polyelectrolytes, and may thereby be susceptible to pharmacologic manipulation.
测试了多种聚阴离子和聚阳离子影响由C56、C7和绵羊红细胞形成EC567的能力。所测试的11种聚阴离子中有6种,包括聚茴香脑磺酸盐、肝素和硫酸葡聚糖,抑制了该反应。相比之下,聚阳离子(测试了5种或7种),包括聚凝胺、鱼精蛋白和聚鸟氨酸,增强了EC567的形成。这种抑制作用与先前描述的称为C567-INH的阴离子血清因子的抑制作用相似,而增强作用似乎涉及血清C567-INH的中和。因此,补体攻击机制的这一步骤似乎易于受到某些聚电解质的调节,从而可能易受药理操作的影响。