Kikumori T, Kambe F, Nagaya T, Funahashi H, Seo H
Department of Endocrinology and Metabolism, Division of Molecular and Cellular Adaptation, Research Institute of Environmental Medicine, Furo-cho, Chikusa-ku, Nagoya University, Nagoya 464-8601, Japan.
Biochem J. 2001 Mar 15;354(Pt 3):573-9. doi: 10.1042/0264-6021:3540573.
We have recently demonstrated that nuclear factor kappaB (NF-kappaB) mediates the tumour necrosis factor alpha (TNF-alpha)-dependent expression of the gene encoding interleukin 6 (IL-6) in rat thyroid FRTL-5 cells cultured in the presence of thyrotropin (TSH). In the present study we investigated how TSH is involved in the activation of NF-kappaB by TNF-alpha in the cells. Electrophoretic mobility-shift assay revealed that, in the absence of TSH, TNF-alpha activated a single protein-DNA complex containing the p50 subunit but not other NF-kappaB subunits such as p65. In contrast, two distinct protein-DNA complexes were activated in the presence of TSH: the faster-migrating complex contained only p50 subunit; the slower-migrating complex consisted of p65-p50 heterodimer. This TSH effect was mimicked by forskolin and thyroid-stimulating antibodies obtained from patients with Graves's disease, suggesting that an increase in intracellular cAMP is responsible for the induction of different NF-kappaBs by TNF-alpha. A transient transfection study with a luciferase reporter gene driven by multimerized NF-kappaB sites demonstrated that TNF-alpha increased the luciferase activities only in the presence of TSH, and that this increase was inhibited by the co-transfection of mutant p65, which prevented the function of wild-type p65 in a dominant-negative manner. Accordingly, TNF-alpha activated the expression of the IL-6 gene in the presence of TSH but not in its absence. Although the expression of the p105 gene, another known target for NF-kappaB, was increased by TNF-alpha in the absence of TSH, the presence of TSH further increased the mRNA level. Taken together, these observations indicate that the presence of TSH is crucial for the NF-kappaB-mediated actions of TNF-alpha on thyroid follicular cells.
我们最近证实,在促甲状腺激素(TSH)存在的情况下培养的大鼠甲状腺FRTL-5细胞中,核因子κB(NF-κB)介导肿瘤坏死因子α(TNF-α)依赖性白细胞介素6(IL-6)编码基因的表达。在本研究中,我们调查了TSH如何参与细胞中TNF-α对NF-κB的激活。电泳迁移率变动分析显示,在没有TSH的情况下,TNF-α激活了一种包含p50亚基的单一蛋白质-DNA复合物,但未激活其他NF-κB亚基,如p65。相反,在有TSH的情况下激活了两种不同的蛋白质-DNA复合物:迁移速度较快的复合物仅包含p50亚基;迁移速度较慢的复合物由p65-p50异二聚体组成。从格雷夫斯病患者获得的福斯可林和促甲状腺抗体模拟了这种TSH效应,表明细胞内cAMP的增加是TNF-α诱导不同NF-κB的原因。用由多聚化NF-κB位点驱动的荧光素酶报告基因进行的瞬时转染研究表明,TNF-α仅在有TSH的情况下增加荧光素酶活性,并且这种增加被突变型p65的共转染所抑制,突变型p65以显性负性方式阻止野生型p65的功能。因此,TNF-α在有TSH的情况下激活IL-6基因的表达,但在没有TSH的情况下则不激活。虽然在没有TSH的情况下,TNF-α增加了另一个已知的NF-κB靶标p105基因的表达,但TSH的存在进一步增加了mRNA水平。综上所述,这些观察结果表明,TSH的存在对于TNF-α对甲状腺滤泡细胞的NF-κB介导的作用至关重要。