Negroni Anna, Prete Enrica, Vitali Roberta, Cesi Vincenzo, Aloi Marina, Civitelli Fortunata, Cucchiara Salvatore, Stronati Laura
Department of Radiobiology and Human Health, ENEA, Rome, Italy.
Department of Radiobiology and Human Health, ENEA, Rome, Italy.
Dig Liver Dis. 2014 Sep;46(9):788-94. doi: 10.1016/j.dld.2014.05.013. Epub 2014 Jun 19.
Endoplasmic reticulum stress and unfolded protein response have been recently associated with the development of inflammatory bowel diseases in adults. We aimed at assessing the involvement of these pathways also in paediatric inflammatory bowel disease by analysing the expression of the main genes involved in endoplasmic reticulum stress and correlating them with the degree of intestinal inflammation.
Real-time PCR and Western blot analysis of the expression of the endoplasmic reticulum stress marker HSPA5 and of selected genes representing the three pathways of unfolded protein response (IRE-XBP1, PERK-ATF4, ATF6p90-p50) in inflamed and uninflamed biopsies from 28 inflammatory bowel disease paediatric patients and 10 controls.
HSPA5, PDIA4, as well as unspliced and spliced XBP1 mRNAs were significantly increased in patients' inflamed colonic mucosa compared to uninflamed mucosa and controls. HSPA5, PDIA4, ATF6, and phospho-IRE proteins were also upregulated, indicating the activation of the IRE-XBP1 and ATF6p90-p50 branches of unfolded protein response. A positive significant correlation between interleukin-8 levels, as a marker of inflammation, and upregulated genes was found in the inflamed colonic mucosa.
A deregulation of the genes involved in the endoplasmic reticulum stress and unfolded protein response pathways may be a key component of the inflammatory response in paediatric patients with inflammatory bowel disease.
内质网应激和未折叠蛋白反应最近被认为与成人炎症性肠病的发生有关。我们旨在通过分析内质网应激相关主要基因的表达,并将其与肠道炎症程度相关联,来评估这些通路在儿童炎症性肠病中的作用。
对28例儿童炎症性肠病患者和10例对照的炎症和非炎症活检组织进行实时PCR和蛋白质印迹分析,检测内质网应激标志物HSPA5以及代表未折叠蛋白反应三条通路(IRE-XBP1、PERK-ATF4、ATF6p90-p50)的选定基因的表达。
与非炎症黏膜和对照相比,患者炎症性结肠黏膜中HSPA5、PDIA4以及未剪接和剪接的XBP1 mRNA显著增加。HSPA5、PDIA4、ATF6和磷酸化IRE蛋白也上调,表明未折叠蛋白反应的IRE-XBP1和ATF6p90-p50分支被激活。在炎症性结肠黏膜中,作为炎症标志物的白细胞介素-8水平与上调基因之间存在显著正相关。
内质网应激和未折叠蛋白反应通路相关基因的失调可能是儿童炎症性肠病患者炎症反应的关键组成部分。