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组蛋白去乙酰化酶对肠上皮细胞中C/EBPδ依赖性反式激活的调控

Regulation of C/EBPdelta-dependent transactivation by histone deacetylases in intestinal epithelial cells.

作者信息

Turgeon Naomie, Valiquette Caroline, Blais Mylène, Routhier Sophie, Seidman Ernest G, Asselin Claude

机构信息

Département d'anatomie et biologie cellulaire, Faculté de médecine et des sciences de la santé, Université de Sherbrooke, Sherbrooke, Québec, Canada J1H 5N4.

出版信息

J Cell Biochem. 2008 Apr 1;103(5):1573-83. doi: 10.1002/jcb.21544.

Abstract

The C/EBPdelta transcription factor is involved in the positive regulation of the intestinal epithelial cell acute phase response. C/EBPdelta regulation by histone deacetylases (HDACs) during the course of inflammation remains to be determined. Our aim was to examine the effect of HDACs on C/EBPdelta-dependent regulation of haptoglobin, an acute phase protein induced in intestinal epithelial cells in response to pro-inflammatory cytokines. HDAC1, HDAC3, and HDAC4 were expressed in intestinal epithelial cells, as determined by Western blot. GST pull-down assays showed specific HDAC1 interactions with the transcriptional activation and the b-ZIP C/EBPdelta domains, while the co-repressor mSin3A interacts with the C-terminal domain. Immunoprecipitation assays confirmed the interaction between HDAC1 and the N-terminal C/EBPdelta amino acid 36-164 domain. HDAC1 overexpression decreased C/EBPdelta transcriptional activity of the haptoglobin promoter, as assessed by transient transfection and luciferase assays. Chromatin immunoprecipitation analysis showed a displacement of HDAC1 from the haptoglobin promoter in response to inflammatory stimuli and an increased acetylation of histone H3 and H4. HDAC1 silencing by shRNA expression increased both basal and IL-1beta-induced haptoglobin mRNA levels in epithelial intestinal cells. Our results suggest that interactions between C/EBPs and HDAC1 negatively regulate C/EBPdelta-dependent haptoglobin expression in intestinal epithelial cells.

摘要

C/EBPδ转录因子参与肠道上皮细胞急性期反应的正向调节。炎症过程中组蛋白去乙酰化酶(HDACs)对C/EBPδ的调节作用尚待确定。我们的目的是研究HDACs对触珠蛋白(一种在肠道上皮细胞中由促炎细胞因子诱导产生的急性期蛋白)的C/EBPδ依赖性调节的影响。通过蛋白质免疫印迹法确定,HDAC1、HDAC3和HDAC4在肠道上皮细胞中表达。谷胱甘肽-S-转移酶(GST)下拉实验显示HDAC1与转录激活域和b-ZIP C/EBPδ结构域存在特异性相互作用,而共抑制因子mSin3A与C末端结构域相互作用。免疫沉淀实验证实了HDAC1与N末端C/EBPδ氨基酸36 - 164结构域之间的相互作用。通过瞬时转染和荧光素酶实验评估,HDAC1过表达降低了触珠蛋白启动子的C/EBPδ转录活性。染色质免疫沉淀分析表明,炎症刺激后HDAC1从触珠蛋白启动子上移位,组蛋白H3和H4的乙酰化增加。通过短发夹RNA(shRNA)表达使HDAC1沉默,增加了肠道上皮细胞中基础和白细胞介素-1β诱导的触珠蛋白mRNA水平。我们的结果表明,C/EBPs与HDAC1之间的相互作用对肠道上皮细胞中C/EBPδ依赖性触珠蛋白表达起负向调节作用。

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