McLeod B, Baker P, Behrends C, Gewurz H
Immunology. 1975 Feb;28(2):379-90.
The stable intermediate complex C56 can initiate the lysis (reactive lysis) of unsensitized erythrocytes (E) by the membrane attack machanism of complement. Certain serum constituents designated C567-INH inhibit reactive lysis by preventing the C567 complex, once formed, from attaching to a membrane surface. It is shown here that microgram quantities of poly-L-lysine (PLL), a synthetic polycation of molecular weight 180,000, can reverse the effests of C567-INH, and thereby potentiate formation of EC567 by erythrocytes, C56 and C7 in whole serum. Erythrocytes exposed to PLL in a preincubation step did not show either increased susceptibility to C567 or resistance to C567-INH, and reversal of C567-IHN by given amounts of PLL was not diminished as cell concentrations were greatly increased, indicating that the effect of PLL was predominantly directed against fluid phase rather than against erythrocyte membrane substrates. The effects of PLL and C567-INH were quantitatively reciprocal. Thus, PLL-induced potentiation of C56-induced lysis is a solute effect which seems to involve direct neutralization of naturally occurring serum inhibitors of the C567 trimolecular complex of complement. The use of PLL thus provides a suitable antagonist for C567-INH in reaction mixtures, and allows evaluation of the role of C567 and C567-INH in a variety of situations involving C-mediated lysis.
稳定的中间复合物C56可通过补体的膜攻击机制引发未致敏红细胞(E)的溶解(反应性溶解)。某些被称为C567-INH的血清成分可通过阻止一旦形成的C567复合物附着于膜表面来抑制反应性溶解。本文表明,微克量的聚-L-赖氨酸(PLL),一种分子量为180,000的合成聚阳离子,可逆转C567-INH的作用,从而增强全血清中红细胞、C56和C7形成EC567的能力。在预孵育步骤中暴露于PLL的红细胞对C567的敏感性既未增加,对C567-INH也无抗性,并且随着细胞浓度大幅增加,给定剂量的PLL对C567-IHN的逆转作用并未减弱,这表明PLL的作用主要针对液相而非红细胞膜底物。PLL和C567-INH的作用在数量上是相互的。因此,PLL诱导的C56诱导溶解的增强是一种溶质效应,似乎涉及对补体C567三分子复合物天然存在的血清抑制剂的直接中和。PLL的使用因此为反应混合物中的C567-INH提供了一种合适的拮抗剂,并允许评估C567和C567-INH在涉及C介导溶解的各种情况下的作用。