First Department of Pediatrics, Semmelweis University, H-1083 Budapest, Hungary.
Pediatr Res. 2010 Aug;68(2):118-22. doi: 10.1203/PDR.0b013e3181e5bc96.
Previously, it has been suggested that hypoxia-inducible factor (HIF) 1 signaling may play determinative role in the maintenance of the barrier function of the intestinal epithelium in inflammatory bowel disease. Our aim was to depict the alteration of HIF-1alpha and related genes in celiac disease (CD) where the importance of the barrier function is well known. Duodenal biopsy specimens were collected from 16 children with untreated CD, 9 children with treated CD and 10 controls. HIF-1alpha, trefoil factor 1 (TFF1), ecto-5-prime nucleotidase (CD73), and multi drug resistance gene 1 (MDR1) mRNA and HIF-1alpha protein expression were determined by real-time PCR and Western blot, respectively. Localization of HIF-1alpha was determined by immunofluorescent staining. We found increased HIF-1alpha and TFF1 mRNA and HIF-1alpha protein expression in the duodenal mucosa of children with untreated CD compared with controls or children with treated CD (p < 0.05). In untreated CD children, HIF-1alpha staining was present in cytoplasmic and nuclear region of the villous enterocytes. In treated CD mRNA expression of CD73 and MDR1 were increased compared with controls (p < 0.01 and 0.05, respectively). Our results of increased mucosal HIF-1alpha expression in CD children suggest the contribution of this signaling pathway in the pathomechanism of CD.
先前有研究提示,缺氧诱导因子(HIF)1 信号通路可能在炎症性肠病(IBD)中发挥决定性作用,维持肠道上皮的屏障功能。我们旨在描述在乳糜泻(CD)中 HIF-1alpha 及相关基因的改变,因为 CD 中屏障功能的重要性是众所周知的。收集了 16 例未经治疗的 CD 患儿、9 例经治疗的 CD 患儿和 10 例对照者的十二指肠活检标本。通过实时 PCR 和 Western blot 分别检测 HIF-1alpha、三叶因子 1(TFF1)、外核苷酸酶 5 型(CD73)和多药耐药基因 1(MDR1)的 mRNA 和 HIF-1alpha 蛋白表达。通过免疫荧光染色确定 HIF-1alpha 的定位。我们发现未经治疗的 CD 患儿的十二指肠黏膜中 HIF-1alpha 和 TFF1 mRNA 以及 HIF-1alpha 蛋白表达增加,与对照组或经治疗的 CD 患儿相比(p<0.05)。在未经治疗的 CD 患儿中,HIF-1alpha 染色存在于绒毛状肠上皮细胞的细胞质和核区域。与对照组相比,经治疗的 CD 患儿的 CD73 和 MDR1 mRNA 表达增加(p<0.01 和 p<0.05)。我们在 CD 患儿中发现黏膜 HIF-1alpha 表达增加的结果表明,该信号通路可能参与 CD 的发病机制。