Thorn R M, Henney C S
J Immunol. 1976 Jan;116(1):146-9.
The role of protein synthesis in the mechanism of T cell-mediated cytolysis has been re-investigated. Cytolytically active (C57BL/L anti-DBA/2) spleen cells treated with pactamycin (10-7 M to 10-6 M) exhibited suppressed protein synthesis (100 +/- 5%), but unimpeded lytic activity. Drug-treated effector cells, incubated for prolonged (up to 24 hr) periods of time in the presence and absence of antigen, showed no siginificant diminution of lytic activity although the incorporation of 3H-leucine into protein was totally ablated. Studies with emetine, another irreversible inhibitor of protein synthesis, gave identical results. These findings are difficult to reconcile with the hypothesis that effector T cells lysis via a soluble protein mediator.
蛋白质合成在T细胞介导的细胞溶解机制中的作用已被重新研究。用 pactamycin(10⁻⁷M至10⁻⁶M)处理的具有细胞溶解活性的(C57BL/L抗DBA/2)脾细胞表现出蛋白质合成受到抑制(100±5%),但细胞溶解活性不受影响。在有和没有抗原存在的情况下,将经药物处理的效应细胞长时间(长达24小时)孵育,尽管3H-亮氨酸掺入蛋白质的过程被完全消除,但细胞溶解活性没有显著降低。用另一种蛋白质合成不可逆抑制剂依米丁进行的研究得出了相同的结果。这些发现很难与效应T细胞通过可溶性蛋白质介质进行裂解的假设相协调。