Zahn Alexandra, Moehle Christoph, Langmann Thomas, Ehehalt Robert, Autschbach Frank, Stremmel Wolfgang, Schmitz Gerd
Department of Gastroenterology, University Hospital of Heidelberg, Im Neuenheimer Feld 410, D-69120 Heidelberg, Germany.
World J Gastroenterol. 2007 Mar 21;13(11):1687-95. doi: 10.3748/wjg.v13.i11.1687.
To study susceptibility genes which may play a potential role in the pathogenesis and etiology of inflammatory bowel disease (IBD).
To identify potential susceptibility genes we performed global gene expression profiling in patients with IBD and control specimens. For determination of an intrinsic gene expression profile in ulcerative colitis (UC) and Crohn's disease (CD) compared to normal subjects, mucosal biopsies of non-inflamed regions of the colon and the terminal ileum were subjected to DNA microarray analysis. Real-time RT-PCR and immunohistochemistry were used for verification of selected regulated candidate genes and a genetic analysis was performed.
We could show that aquaporin-8 (AQP8) mRNA and protein levels were significantly increased in the colon of UC patients compared to controls. Genetic analysis of the six exons and the promoter region of AQP8, however, revealed no mutations or polymorphisms in IBD patients.
Our results suggest that upregulation of AQP8 in the colon of UC patients represents a secondary phenomenon which may, due to altered water exchange of the distal intestinal mucosa, disturb the physiologic colonic mucus barrier and thus lead to chronic inflammation and ulceration.
研究可能在炎症性肠病(IBD)发病机制和病因学中发挥潜在作用的易感基因。
为了鉴定潜在的易感基因,我们对IBD患者和对照样本进行了全基因组表达谱分析。为了确定与正常受试者相比,溃疡性结肠炎(UC)和克罗恩病(CD)的内在基因表达谱,对结肠和回肠末端非炎症区域的黏膜活检组织进行DNA微阵列分析。采用实时逆转录聚合酶链反应(RT-PCR)和免疫组织化学方法对选定的调控候选基因进行验证,并进行遗传分析。
我们发现,与对照组相比,UC患者结肠中aquaporin-8(AQP8)的mRNA和蛋白水平显著升高。然而,对AQP8的六个外显子和启动子区域进行遗传分析后发现,IBD患者中没有突变或多态性。
我们的结果表明,UC患者结肠中AQP8的上调是一种继发现象,可能由于远端肠黏膜水交换改变,扰乱了生理性结肠黏液屏障,从而导致慢性炎症和溃疡形成。