Altmeyer A, Staruch M J, Cofano F, Landolfo S, Dumont F J
Department of Immunology, Merck, Sharp and Dohme Research Laboratories, Rahway, New Jersey 07065.
Cell Immunol. 1991 Nov;138(1):94-107. doi: 10.1016/0008-8749(91)90135-x.
The cell surface Ly-6E antigen, known to play a role in T cell activation, is up-regulated by IFNs. In the present study, we investigated the possible interactions between IFNs and other cytokines in this regulation. As a model system, we used the YAC T cell lymphoma, in which Ly-6E is normally absent but can be highly induced both at the mRNA and surface protein levels by IFN-gamma or IFN-alpha/beta. The combination of the two IFNs was found to result in markedly synergistic Ly-6E induction in this cell line. Moreover, mutants of YAC cells were isolated that did not respond to the Ly-6E-inducing action of IFN-gamma or IFN-alpha/beta alone but did respond to their combination. Such a synergistic interaction is consistent with the notion that the two IFN types utilize different intracellular mechanisms to induce Ly-6E expression. Ly-6E induction mediated by IFN-gamma or IFN-alpha/beta was also enhanced by cotreatment with TNF-alpha or IL-1 alpha, which by themselves had no detectable Ly-6E-inducing effect. These two cytokines similarly synergized with IFNs to trigger a response in several Ly-6E-induction-deficient mutants. However, their action could be dissociated in one mutant (B54) where the response to IFN-alpha/beta was enhanced by TNF-alpha, but not by IL-1 alpha. Altogether, these data indicate that Ly-6E antigen expression is regulated by the interaction of several inflammatory cytokines, which may provide a mechanism for the local modulation of T cell activation. The YAC cell mutants described here should facilitate further analysis of the molecular bases of Ly-6E regulation.
细胞表面Ly-6E抗原已知在T细胞活化中发挥作用,可被干扰素上调。在本研究中,我们调查了干扰素与其他细胞因子在这种调节中的可能相互作用。作为一个模型系统,我们使用了YAC T细胞淋巴瘤,其中Ly-6E通常不存在,但可被γ干扰素或α/β干扰素在mRNA和表面蛋白水平高度诱导。发现这两种干扰素的组合在该细胞系中导致显著的协同诱导Ly-6E。此外,分离出了YAC细胞突变体,它们对单独的γ干扰素或α/β干扰素的Ly-6E诱导作用无反应,但对它们的组合有反应。这种协同相互作用与两种干扰素类型利用不同的细胞内机制诱导Ly-6E表达的观点一致。用肿瘤坏死因子-α或白细胞介素-1α共处理也增强了γ干扰素或α/β干扰素介导的Ly-6E诱导,而它们自身没有可检测到的Ly-6E诱导作用。这两种细胞因子同样与干扰素协同作用,在几个Ly-6E诱导缺陷的突变体中引发反应。然而,它们的作用在一个突变体(B54)中可以分开,在该突变体中,肿瘤坏死因子-α增强了对α/β干扰素的反应,但白细胞介素-1α没有。总之,这些数据表明Ly-6E抗原表达受几种炎性细胞因子相互作用的调节,这可能为T细胞活化的局部调节提供一种机制。这里描述的YAC细胞突变体应有助于进一步分析Ly-6E调节的分子基础。