Borghaei Ruth C, Chambers Mariah
Department of Biochemistry and Molecular Biology, Philadelphia College of Osteopathic Medicine, 4170 City Avenue, Philadelphia, PA 19131, USA.
Pathol Lab Med Int. 2009 Aug 1;1:7-12. doi: 10.2147/plmi.s6249.
Zinc-binding protein-89 (ZBP-89; ZNF148, BERF-1, BFCOL-1) is a zinc-finger transcription factor of the Kruppel family. It has been shown to regulate the expression of a number of genes, acting as either an activator or repressor of gene expression, depending on the context. It is over-expressed in several cancers, but has been shown to be involved in apoptosis and to have a negative influence on cell growth in part by interactions with p53. Previously, ZBP-89 was shown to activate transcription of the matrix metalloproteinase-3 (MMP-3) gene by binding to a polymorphic promoter element in competition with nuclear factor kappaB (NF-kappaB). NF-kappaB is known to be a key regulator of the inflammatory response, but relatively little is known about regulation of ZBP-89. In order to ascertain whether ZBP-89 is regulated during inflammation, we designed experiments to determine whether and to what extent ZBP-89 levels are affected by inflammatory cytokines. Here we show that ZBP-89 mRNA and protein expression are significantly inhibited in human fibroblasts by the inflammatory cytokine interleukin-1beta. Since any change in the levels of ZBP-89 would presumably impact the regulation of MMP-3 and other ZBP-89 target genes, these results provide important insight into mechanisms involved in fine-tuning the immune response.
锌结合蛋白89(ZBP - 89;ZNF148、BERF - 1、BFCOL - 1)是一种克鲁ppel家族的锌指转录因子。已表明它可调节多个基因的表达,根据具体情况,它既可以作为基因表达的激活剂,也可以作为抑制剂。它在几种癌症中过度表达,但已证明它参与细胞凋亡,并且部分通过与p53相互作用对细胞生长产生负面影响。此前,已表明ZBP - 89通过与核因子κB(NF - κB)竞争结合一个多态性启动子元件来激活基质金属蛋白酶3(MMP - 3)基因的转录。已知NF - κB是炎症反应的关键调节因子,但对ZBP - 89的调节了解相对较少。为了确定ZBP - 89在炎症过程中是否受到调节,我们设计了实验来确定炎症细胞因子是否以及在何种程度上影响ZBP - 89的水平。在此我们表明,炎症细胞因子白细胞介素 - 1β可显著抑制人成纤维细胞中ZBP - 89的mRNA和蛋白质表达。由于ZBP - 89水平的任何变化可能会影响MMP - 3和其他ZBP - 89靶基因的调节,这些结果为微调免疫反应所涉及的机制提供了重要见解。