Morinaga Y, Suzuki H, Takatsuki F, Akiyama Y, Taniyama T, Matsushima K, Onozaki K
Department of Microbiology, University of Tsukuba, Ibaraki, Japan.
J Immunol. 1989 Dec 1;143(11):3538-42.
The role of IL-6 in the antiproliferative effect of IL-1 for tumor cell lines was investigated using IL-1-sensitive cell lines. Human recombinant IL-1 alpha and IL-6 both inhibited the growth of an IL-1-sensitive cloned human melanoma cell line (A375-C6). However, IL-1 has greater maximum growth inhibitory activity than IL-6. Conditioned medium of the tumor cells that were treated with IL-1 contained IL-6 as determined by ELISA. Northern blot analysis revealed that IL-6 mRNA expression increased in IL-1-treated cells. In addition, antibody against human IL-6 neutralized about 50% of the antiproliferative effect of IL-1. The growth of an IL-1-resistant clone of A375 cells (A375-C5), which cannot be shown to express any detectable IL-1R, was inhibited by IL-6 to the same degree as A375-C6 cells. The A375-C5 cell line did not produce IL-6 or increase IL-6 mRNA after stimulation with IL-1. These results indicate that IL-6 mediates in part the antiproliferative effect of IL-1 on A375-C6 cells by acting as an autocrine antiproliferative factor. IL-1 also inhibited the growth of a malignant human mammary cell line (MDA-MB-415). IL-6 exhibited only slight growth inhibition in this cell line. Neither IL-6 production nor IL-6 mRNA expression was induced in this cell line by IL-1. Antibody against IL-6 did not neutralize the antiproliferative effect of IL-1. Therefore, for MDA-MB-415 cells IL-6 appeared not to be involved in the antiproliferative effect of IL-1. These results indicate that the antiproliferative effect of IL-1 involves at least two pathways, one IL-6 dependent and another IL-6 independent. The contribution of IL-6 to the antiproliferative effect of TNF was also examined. IL-6 appeared not to play a role in the antiproliferative effect of TNF in these cell lines.
利用白细胞介素-1(IL-1)敏感细胞系研究了IL-6在IL-1对肿瘤细胞系的抗增殖作用中的角色。重组人IL-1α和IL-6均抑制了一株对IL-1敏感的克隆化人黑色素瘤细胞系(A375-C6)的生长。然而,IL-1的最大生长抑制活性比IL-6更强。经ELISA测定,用IL-1处理的肿瘤细胞的条件培养基中含有IL-6。Northern印迹分析显示,IL-1处理的细胞中IL-6 mRNA表达增加。此外,抗人IL-6抗体中和了约50%的IL-1的抗增殖作用。A375细胞的一个对IL-1耐药的克隆(A375-C5),其未表现出可检测到的任何IL-1受体表达,其生长受到IL-6的抑制,抑制程度与A375-C6细胞相同。A375-C5细胞系在用IL-1刺激后不产生IL-6或增加IL-6 mRNA。这些结果表明,IL-6通过作为自分泌抗增殖因子,部分介导了IL-1对A375-C6细胞的抗增殖作用。IL-1也抑制了一株恶性人乳腺细胞系(MDA-MB-415)的生长。IL-6在该细胞系中仅表现出轻微的生长抑制。IL-1未诱导该细胞系产生IL-6或表达IL-6 mRNA。抗IL-6抗体未中和IL-1的抗增殖作用。因此,对于MDA-MB-415细胞,IL-6似乎未参与IL-1的抗增殖作用。这些结果表明,IL-1的抗增殖作用至少涉及两条途径,一条依赖IL-6,另一条不依赖IL-6。还研究了IL-6对肿瘤坏死因子(TNF)抗增殖作用的贡献。在这些细胞系中,IL-6似乎未在TNF的抗增殖作用中发挥作用。