Ardite E, Panés J, Miranda M, Salas A, Elizalde J I, Sans M, Arce Y, Bordas J M, Fernández-Checa J C, Piqué J M
Consejo Superior Investigaciones Científicas, Barcelona, Spain.
Br J Pharmacol. 1998 Jun;124(3):431-3. doi: 10.1038/sj.bjp.0701887.
Nuclear factor kappB (NFkappaB) is a transcription factor that controls several genes important for immunity and inflammation. The aim of this study was to assess if activation of NFkappaB plays a role in the pathogenesis of inflammatory bowel disease (IBD), and whether steroid treatment affects NFkappaB activation. Activation of NFkappaB was analysed in colon biopsy samples of 13 patients with active IBD (8 Crohn's colitis, 5 ulcerative colitis) by electrophoretic mobility-shift assays, under basal conditions and 3 weeks after treatment with 0.75 mg kg(-1) day(-1) prednisolone. The presence of interleukin-8 mRNA in biopsies was assessed by RT-PCR. A specific NFkappaB band was present in all nuclear extracts from inflamed mucosa, whereas the band was barely detectable in uninflamed colonic mucosa. NFkappaB bands were super-shifted by antibodies against p50 subunit, whereas antibodies against p65, p52, c-Rel, or Rel B did not modify the mobility of the band. Increased interleukin-8 mRNA was detected at the same sites of NFkappaB activation. Steroid-induced healing of colonic inflammation was associated with disappearance of NFkappaB from nuclear extracts. These results support the notion that NFkappaB plays an important role in the pathogenesis of IBD, and that blockade of NFkappaB activation is one of the mechanisms by which steroids suppress the inflammatory cascade in IBD.
核因子κB(NFκB)是一种转录因子,可调控多个对免疫和炎症至关重要的基因。本研究的目的是评估NFκB的激活是否在炎症性肠病(IBD)的发病机制中起作用,以及类固醇治疗是否会影响NFκB的激活。通过电泳迁移率变动分析,在基础条件下以及用0.75 mg·kg⁻¹·天⁻¹泼尼松龙治疗3周后,对13例活动性IBD患者(8例克罗恩结肠炎,5例溃疡性结肠炎)的结肠活检样本中NFκB的激活情况进行了分析。通过逆转录聚合酶链反应(RT-PCR)评估活检样本中白细胞介素-8 mRNA的存在情况。在所有炎症黏膜的核提取物中均存在一条特异性的NFκB条带,而在未发炎的结肠黏膜中几乎检测不到该条带。抗p50亚基的抗体使NFκB条带发生超迁移,而抗p65、p52、c-Rel或Rel B的抗体并未改变条带的迁移率。在NFκB激活的相同部位检测到白细胞介素-8 mRNA增加。类固醇诱导的结肠炎症愈合与核提取物中NFκB的消失相关。这些结果支持了NFκB在IBD发病机制中起重要作用的观点,并且NFκB激活的阻断是类固醇抑制IBD炎症级联反应的机制之一。