Zhang Y H, Lin J X, Vilcek J
Department of Microbiology, New York University Medical Center, New York 10016.
Mol Cell Biol. 1990 Jul;10(7):3818-23. doi: 10.1128/mcb.10.7.3818-3823.1990.
Using variable-length deletion constructs of the 5'-flanking region of the human interleukin-6 (IL-6) gene linked to the chloramphenicol acetyltransferase gene, we showed that the region from positions -109 to -50 mediated the bulk of the response to tumor necrosis factor (TNF) or interleukin-1 (IL-1), while it was less responsive to forskolin. DNA mobility shift assays and DNase I footprinting analysis identified a nuclear protein from TNF- or IL-1-treated fibroblasts that bound to a region comprising a kappa B-like element located between positions -72 and -63 on the IL-6 gene. On the basis of these and other experiments, we conclude that TNF and IL-1 apparently activate IL-6 gene expression by closely related mechanisms involving activation of a NF-kappa B-like factor, whereas the pathway of IL-6 induction by forskolin is, in part, different.
利用与氯霉素乙酰转移酶基因相连的人白细胞介素-6(IL-6)基因5'-侧翼区的可变长度缺失构建体,我们发现从-109至-50位的区域介导了对肿瘤坏死因子(TNF)或白细胞介素-1(IL-1)的大部分应答,而其对福司可林的反应较弱。DNA迁移率变动分析和DNase I足迹分析鉴定出一种来自经TNF或IL-1处理的成纤维细胞的核蛋白,它与一个包含位于IL-6基因-72至-63位之间的κB样元件的区域结合。基于这些及其他实验,我们得出结论,TNF和IL-1显然通过涉及激活NF-κB样因子的密切相关机制来激活IL-6基因表达,而福司可林诱导IL-6的途径则部分不同。