Orosz C G, Roopenian D C, Bach F H
J Immunol. 1983 Jun;130(6):2499-501.
Prolonged contact with nanomole to micromole concentrations of the tumor promoter phorbol myristate acetate causes a significant reduction in the lytic activity of cloned cytolytic T cells. Diminished lysis is apparent even in the presence of agglutinating lectins. PMA does not exert this effect by minimizing clone viability. In fact, these concentrations of PMA cause significant potentiation of antigen-driven proliferation for many of these same clones. The PMA-mediated loss of cytolysis is reversible. Although contact with antigen does not induce or enhance reexpression of cytolysis, PMA-treated cytolytic T cell clones display normal cytolytic activity after contact with lymphokines.
与纳摩尔至微摩尔浓度的肿瘤启动子佛波酯肉豆蔻酸酯乙酸盐长时间接触,会导致克隆的细胞毒性T细胞的裂解活性显著降低。即使存在凝集素,裂解作用减弱仍很明显。佛波酯肉豆蔻酸酯乙酸盐并非通过降低克隆的活力来发挥这种作用。事实上,这些浓度的佛波酯肉豆蔻酸酯乙酸盐会显著增强许多相同克隆的抗原驱动增殖。佛波酯肉豆蔻酸酯乙酸盐介导的细胞溶解丧失是可逆的。虽然与抗原接触不会诱导或增强细胞溶解的重新表达,但经佛波酯肉豆蔻酸酯乙酸盐处理的细胞毒性T细胞克隆在与淋巴因子接触后会表现出正常的细胞溶解活性。