Department of Biochemistry and Molecular Biology, University of Valencia, 46100, Valencia, Burjassot, Spain.
Cell Mol Life Sci. 2010 May;67(10):1687-97. doi: 10.1007/s00018-010-0272-3. Epub 2010 Feb 4.
Tauhe expression of the critical initiator cytokine TNF-alpha was strongly upregulated in vivo in acute necrotic pancreatitis (AP) in rodents and in vitro in TNF-alpha activated acinar AR42J cells. Upregulation of tnf-alpha, inos, icam-1 and il-6 occurred both in TNF-alpha receptor 1 and 2 knock-out mice, but not in TNF-alpha knock-out mice, in cerulein-induced acute pancreatitis. Chromatin immunoprecipitation analysis showed that transcriptional factors (ELK-1, SP1, NF-kappaB and EGR-1) and chromatin modification complexes (HDAC1, HDAC2, GCN5, PCAF and CBP) were recruited and/or released from the promoter in a strictly ordered mechanism. Activation of tnf-alpha gene was also accompanied by an ordered increased level of histone H3K9, H3K14 and H3K18-acetylation and H3K4 methylation, as well as H4K5 acetylation. A better knowledge of the molecular mechanisms that control tnf-alpha gene regulation will provide deeper understanding of the initiation and development of the inflammatory processes occurring in acute pancreatitis triggered by TNF-alpha cytokine.
在鼠类急性坏死性胰腺炎(AP)的体内和 TNF-α 激活的胰腺腺泡 AR42J 细胞的体外实验中,Tau 蛋白表达关键启动子细胞因子 TNF-α明显上调。在雨蛙肽诱导的急性胰腺炎中,TNF-α 受体 1 和 2 敲除小鼠以及 TNF-α 敲除小鼠中均发生了 tnf-α、inos、icam-1 和 il-6 的上调。染色质免疫沉淀分析表明,转录因子(ELK-1、SP1、NF-κB 和 EGR-1)和染色质修饰复合物(HDAC1、HDAC2、GCN5、PCAF 和 CBP)被募集并/或从启动子中以严格有序的机制释放。TNF-α 基因的激活还伴随着组蛋白 H3K9、H3K14 和 H3K18-乙酰化以及 H3K4 甲基化和 H4K5 乙酰化的有序增加。更好地了解控制 TNF-α 基因调控的分子机制将深入了解由 TNF-α 细胞因子引发的急性胰腺炎中炎症过程的启动和发展。