Ramos O F, Masucci M G, Bejarano M T, Klein E
Immunobiology. 1983 Dec;165(5):403-14. doi: 10.1016/S0171-2985(83)80064-3.
The tumor promoters 12-13-phorbol-dibutyrate, P(Bu)2, and 12-O-tetradecanoylphorbol-13-acetate, TPA, were shown to augment the cytotoxic potential of human blood lymphocytes with low cell density. In kinetics experiments the enhancing effect was preceded by an initial suppression lasting for about 2 hours. Admixture of mononuclear adherent cells abrogated the P(Bu)2 effect in a dose dependent way. P(Bu)2 altered the sensitivity of K562 cells to the cytotoxic effect. Short term pretreatment increased the sensitivity, but after longer pretreatment the cells became resistant. The results show that tumor promoters can influence the cytolytic system at different levels. By acting directly on the lymphocytes they potentiate the lytic function. When mixed mononuclear populations are used, this effect may be counteracted via activation of the suppressive functions of monocytes. In addition, the target cell sensitivity can also be modulated. As a result, the final outcome of phorbol treatment depends on the strength, kinetics and the mode of its effects on the interactants.
肿瘤促进剂12 - 13 - 佛波醇二丁酸酯(P(Bu)2)和12 - O - 十四酰佛波醇 - 13 - 乙酸酯(TPA)已被证明可增强低细胞密度下人血淋巴细胞的细胞毒性潜力。在动力学实验中,增强作用之前有一个持续约2小时的初始抑制阶段。单核贴壁细胞的混合以剂量依赖的方式消除了P(Bu)2的作用。P(Bu)2改变了K562细胞对细胞毒性作用的敏感性。短期预处理增加了敏感性,但长期预处理后细胞变得耐药。结果表明,肿瘤促进剂可在不同水平影响溶细胞系统。通过直接作用于淋巴细胞,它们增强了裂解功能。当使用混合单核细胞群体时,这种作用可能通过激活单核细胞的抑制功能而被抵消。此外,靶细胞的敏感性也可被调节。因此,佛波醇处理的最终结果取决于其对相互作用者的作用强度、动力学和方式。