Pietz Grzegorz, De Rituparna, Hedberg Maria, Sjöberg Veronika, Sandström Olof, Hernell Olle, Hammarström Sten, Hammarström Marie-Louise
Department of Clinical Microbiology, Immunology, Umeå University, Umeå, Sweden.
Department of Clinical Sciences, Pediatrics, Umeå University, Umeå, Sweden.
PLoS One. 2017 Sep 21;12(9):e0185025. doi: 10.1371/journal.pone.0185025. eCollection 2017.
BACKGROUND & AIMS: Celiac disease is a chronic inflammatory disease of the small intestine mucosa due to permanent intolerance to dietary gluten. The aim was to elucidate the role of small intestinal epithelial cells in the immunopathology of celiac disease in particular the influence of celiac disease-associated bacteria.
Duodenal biopsies were collected from children with active celiac disease, treated celiac disease, and clinical controls. Intestinal epithelial cells were purified and analyzed for gene expression changes at the mRNA and protein levels. Two in vitro models for human intestinal epithelium, small intestinal enteroids and polarized tight monolayers, were utilized to assess how interferon-γ, interleukin-17A, celiac disease-associated bacteria and gluten influence intestinal epithelial cells.
More than 25 defense-related genes, including IRF1, SPINK4, ITLN1, OAS2, CIITA, HLA-DMB, HLA-DOB, PSMB9, TAP1, BTN3A1, and CX3CL1, were significantly upregulated in intestinal epithelial cells at active celiac disease. Of these genes, 70% were upregulated by interferon-γ via the IRF1 pathway. Most interestingly, IRF1 was also upregulated by celiac disease-associated bacteria. The NLRP6/8 inflammasome yielding CASP1 and biologically active interleukin-18, which induces interferon-γ in intraepithelial lymphocytes, was expressed in intestinal epithelial cells.
A key factor in the epithelial reaction in celiac disease appears to be over-expression of IRF1 that could be inherent and/or due to presence of undesirable microbes that act directly on IRF1. Dual activation of IRF1 and IRF1-regulated genes, both directly and via the interleukin-18 dependent inflammasome would drastically enhance the inflammatory response and lead to the pathological situation seen in active celiac disease.
乳糜泻是一种由于对膳食麸质永久不耐受而导致的小肠黏膜慢性炎症性疾病。本研究旨在阐明小肠上皮细胞在乳糜泻免疫病理学中的作用,尤其是与乳糜泻相关细菌的影响。
收集活动性乳糜泻患儿、已治疗乳糜泻患儿及临床对照儿童的十二指肠活检组织。纯化肠道上皮细胞并分析其mRNA和蛋白质水平的基因表达变化。利用两种人肠上皮体外模型,即小肠类器官和极化紧密单层细胞,评估干扰素-γ、白细胞介素-17A、与乳糜泻相关细菌及麸质对肠道上皮细胞的影响。
超过25个与防御相关的基因,包括IRF1、SPINK4、ITLN1、OAS2、CIITA、HLA-DMB、HLA-DOB、PSMB9、TAP1、BTN3A1和CX3CL1,在活动性乳糜泻的肠道上皮细胞中显著上调。其中70%的基因通过IRF1途径被干扰素-γ上调。最有趣的是,IRF1也被与乳糜泻相关的细菌上调。产生半胱天冬酶-1和具有生物活性的白细胞介素-18的NLRP6/8炎性小体在肠道上皮细胞中表达,白细胞介素-18可诱导上皮内淋巴细胞产生干扰素-γ。
乳糜泻上皮反应的一个关键因素似乎是IRF1的过度表达,这可能是内在的和/或由于直接作用于IRF1的不良微生物的存在。IRF1及其调控基因的双重激活,无论是直接激活还是通过白细胞介素-18依赖性炎性小体激活,都将极大地增强炎症反应,并导致活动性乳糜泻中所见的病理状况。