Haliotis T, Werkmeister J A, Louwman I, Liao S K, Matthews J, Riopelle R, Pross H F, Holden J J, White B N, Smith A
J Natl Cancer Inst. 1984 May;72(5):991-8.
Culture of the human melanoma cell line MeWo in the presence of 1 mM theophylline was associated with an increase in susceptibility to natural killer (NK)-mediated cytolysis. The phenomenon was detected as early as 72 hours after initiation of theophylline treatment, reaching maximum values at 3-4 weeks and remaining stable for longer than 3 months of testing, provided the cells were maintained in the presence of theophylline. The alteration in target sensitivity was selective for NK-mediated cytolysis, since other mechanisms of cell-mediated cytolysis, including antibody-dependent cell-mediated cytotoxicity and monocyte-mediated and lectin-induced cytolysis, were comparable between untreated and treated cells. The enhanced susceptibility of theophylline-treated cultures to NK lysis, as compared to NK lysis susceptibility of untreated MeWo cells, was not significantly changed by pretreatment of effector lymphocytes with interferon. Evidence for differentiation in theophylline-treated cultures was obtained. In addition, however, cytofluorometric and karyologic analysis revealed the existence of two subpopulations of differing ploidy in the MeWo line. The hypodiploid, NK-sensitive subpopulation, bearing homogeneously staining regions on two chromosomes, could be selected by growth in theophylline. Therefore, selection of subpopulations in heterogeneous tumor cell lines by chemical inducers suggests an alternative and novel mechanism for enhancement of NK sensitivity.
在1 mM氨茶碱存在的情况下培养人黑色素瘤细胞系MeWo,会使其对自然杀伤(NK)介导的细胞溶解敏感性增加。早在氨茶碱处理开始后72小时就检测到了这种现象,在3 - 4周时达到最大值,并且在长达3个月以上的测试中保持稳定,前提是细胞维持在氨茶碱存在的环境中。靶细胞敏感性的改变对NK介导的细胞溶解具有选择性,因为其他细胞介导的细胞溶解机制,包括抗体依赖性细胞介导的细胞毒性、单核细胞介导的和凝集素诱导的细胞溶解,在未处理和处理过的细胞之间是相当的。与未处理的MeWo细胞的NK溶解敏感性相比,氨茶碱处理的培养物对NK溶解的增强敏感性,在用干扰素预处理效应淋巴细胞后没有显著变化。获得了氨茶碱处理的培养物中细胞分化的证据。然而,此外,细胞荧光分析和核型分析显示MeWo细胞系中存在两个不同倍体的亚群。在两条染色体上带有均匀染色区的亚二倍体、NK敏感亚群,可以通过在氨茶碱中生长来选择。因此,通过化学诱导剂在异质性肿瘤细胞系中选择亚群,提示了一种增强NK敏感性的替代且新颖的机制。