Hudig D, Redelman D, Minning L, Carine K
J Immunol. 1984 Jul;133(1):408-14.
K-76 COONa is a 440 m.w. fungal product that can inhibit complement activity of C5 and Factor I. K-76 COONa abrogated both human natural killer (NK) cell activity and antibody-dependent cell-mediated cytotoxicity (ADCC) (ID50 approximately 1.5 mM). To be effective, K-76 COONa had to be present during the assay, because pretreatment of lymphocytes with highly inhibitory concentrations of K-76 COONa did not inhibit cytolysis. The monocarboxylic K-76 derivative was more inhibitory to NK than the dicarboxylic derivative. This relative efficacy is similar to that observed for inhibition of complement lysis. K-76 COONa inhibited NK when added before NK conjugate formation, but had little effect when added after conjugate formation. The compound also inhibited the formation of conjugates by NK and K cells. Therefore, this reagent selectively affected events that occurred between the initial effector-target cell interactions and the formation of stable conjugates. It had little influence on the post-binding "lethal hit" stage of cytolysis. These data imply a) that if any molecules similar to C5 are activated during the "lethal hit" stage of cytolysis, then they are inaccessible to K-76 COONa , and b) that C3bi-like molecules may be involved in lymphocyte binding.
K-76 羧酸钠是一种分子量为 440 的真菌产物,它能够抑制 C5 和补体 I 因子的补体活性。K-76 羧酸钠可消除人类自然杀伤(NK)细胞活性以及抗体依赖性细胞介导的细胞毒性(ADCC)(半数抑制浓度约为 1.5 mM)。为了发挥作用,K-76 羧酸钠必须在检测过程中存在,因为用高抑制浓度的 K-76 羧酸钠预处理淋巴细胞并不能抑制细胞溶解。单羧酸 K-76 衍生物对 NK 的抑制作用比二羧酸衍生物更强。这种相对效力与补体溶解抑制中观察到的情况相似。在 NK 结合物形成之前添加 K-76 羧酸钠可抑制 NK,但在结合物形成后添加则几乎没有效果。该化合物还抑制 NK 细胞与 K 细胞结合物的形成。因此,这种试剂选择性地影响了初始效应细胞 - 靶细胞相互作用与稳定结合物形成之间发生的事件。它对细胞溶解的结合后“致命一击”阶段影响很小。这些数据表明:a)如果在细胞溶解的“致命一击”阶段有任何类似于 C5 的分子被激活,那么它们对 K-76 羧酸钠来说是不可及的;b)类似 C3bi 的分子可能参与淋巴细胞结合。