促炎细胞因子
炎症性肠病
肿瘤坏死因子α
溃疡性结肠炎
转录因子
细胞因子
下调和上调
NF-κB
免疫学
癌症研究
白细胞介素6
基因表达
白细胞介素
分子生物学
生物
基因
医学
炎症
疾病
内科学
遗传学
作者
Markus F. Neurath,Ivan J. Fuss,G. Schürmann,Sven Pettersson,KARL ARNOLD,H. Müller-Lobeck,Warren Strober,Christian Herfarth,Karl-Hermann Meyer zum Büschenfelde
标识
DOI:10.1111/j.1749-6632.1998.tb11119.x
摘要
ABSTRACT: We examined the expression of the transcription factor NF‐κB, a nuclear trans ‐acting factor known to play a key role in cytokine gene regulation, in patients with inflammatory bowel disease (IBD). It was found that LP macrophages in Crohn's disease (CD) and ulcerative colitis (UC) display high levels of NF‐κB DNA‐binding activity accompanied by an increased production of interleukin (IL)‐1, IL‐6, and tumor necrosis factor (TNF)α. Western blot studies showed an increased expression of the p50 and c‐rel subunits of NF‐κB; however, the most striking finding was an increased expression level of NF‐κB p65 in patients with CD and UC. Selective downregulation of p65 in IBD macrophages by a specific antisense phosphorothioate oligonucleotide was sufficient to considerably reduce production of proinflammatory cytokines. These results demonstrate a characteristic increase of NF‐κB binding levels in patients with IBD. The data suggest that antisense DNA targeting NF‐κB p65 can be used as a novel molecular approach for the treatment of patients with IBD.
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