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肝细胞中NF-IL6与C/EBP的相互表达:NF-IL6可能参与急性期蛋白基因表达。

Reciprocal expression of NF-IL6 and C/EBP in hepatocytes: possible involvement of NF-IL6 in acute phase protein gene expression.

作者信息

Isshiki H, Akira S, Sugita T, Nishio Y, Hashimoto S, Pawlowski T, Suematsu S, Kishimoto T

机构信息

Institute for Molecular and Cellular Biology, Osaka University, Japan.

出版信息

New Biol. 1991 Jan;3(1):63-70.

PMID:1710143
Abstract

The initial phase of inflammation is accompanied by dramatic changes in the concentrations of certain plasma proteins. Interleukin-6 (IL-6) is an important inducer of these acute phase proteins at the transcriptional level. The recently cloned nuclear factor NF-IL6, a potent trans-acting regulator of IL-6 gene expression, has a region that is highly homologous to the liver-specific transcriptional factor C/EBP. Both factors recognize the same nucleotide sequence. In this study the recombinant NF-IL6 was shown to interact with the IL-6-responsive elements (IL-6REs) identified in the promoter region of several acute phase protein genes whose activity increases during the acute phase reaction. Furthermore, in competition experiments, formation of all the DNA-protein complexes by the IL-6RE and IL-6-treated hepatoma cell extracts was specifically decreased by adding either the 14-bp NF-IL6 binding motif identified in the IL-6 promoter or the antibody against the recombinant NF-IL6. NF-IL6 was expressed at a minor level in mouse liver, but was dramatically induced after stimulation with IL-6. In contrast, the amount of C/EBP mRNA decreased considerably after IL-6 stimulation. These results indicate that the NF-IL6 that regulated IL-6 expression was also involved in regulation of expression of the acute phase protein genes. The ability of NF-IL6 to replace C/EBP may explain the positive and negative acute phase responses induced by IL-6.

摘要

炎症的初始阶段伴随着某些血浆蛋白浓度的显著变化。白细胞介素-6(IL-6)是这些急性期蛋白在转录水平上的重要诱导物。最近克隆的核因子NF-IL6是IL-6基因表达的一种强效反式作用调节因子,它有一个区域与肝脏特异性转录因子C/EBP高度同源。这两种因子识别相同的核苷酸序列。在本研究中,重组NF-IL6被证明可与在几种急性期蛋白基因启动子区域中鉴定出的IL-6反应元件(IL-6REs)相互作用,这些基因在急性期反应期间活性增加。此外,在竞争实验中,通过添加在IL-6启动子中鉴定出的14bp NF-IL6结合基序或抗重组NF-IL6抗体,可特异性降低IL-6RE与经IL-6处理的肝癌细胞提取物形成的所有DNA-蛋白质复合物。NF-IL6在小鼠肝脏中表达水平较低,但在IL-6刺激后被显著诱导。相反,IL-6刺激后C/EBP mRNA的量显著下降。这些结果表明,调节IL-6表达的NF-IL6也参与了急性期蛋白基因表达的调节。NF-IL6替代C/EBP的能力可能解释了IL-6诱导的正负急性期反应。

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