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本文引用的文献

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Multicenter analysis of fecal microbiota profiles in Japanese patients with Crohn's disease.日本克罗恩病患者粪便微生物群特征的多中心分析。
J Gastroenterol. 2012 Dec;47(12):1298-307. doi: 10.1007/s00535-012-0605-0. Epub 2012 May 11.
2
IL-37: a new anti-inflammatory cytokine of the IL-1 family.IL-37:IL-1 家族的一种新抗炎细胞因子。
Eur Cytokine Netw. 2011 Sep;22(3):127-47. doi: 10.1684/ecn.2011.0288.
3
Interleukin 37 expression protects mice from colitis.白细胞介素 37 的表达可保护小鼠免受结肠炎的影响。
Proc Natl Acad Sci U S A. 2011 Oct 4;108(40):16711-6. doi: 10.1073/pnas.1111982108. Epub 2011 Aug 22.
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CXCL10/IP-10 in infectious diseases pathogenesis and potential therapeutic implications.细胞趋化因子 10/干扰素诱导蛋白 10 在感染性疾病发病机制中的作用及其潜在的治疗意义。
Cytokine Growth Factor Rev. 2011 Jun;22(3):121-30. doi: 10.1016/j.cytogfr.2011.06.001. Epub 2011 Jul 29.
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Type 2 innate immune responses and the natural helper cell.2 型先天免疫反应和自然辅助细胞。
Immunology. 2011 Apr;132(4):475-81. doi: 10.1111/j.1365-2567.2011.03413.x. Epub 2011 Feb 16.
6
Comparison of the fecal microbiota profiles between ulcerative colitis and Crohn's disease using terminal restriction fragment length polymorphism analysis.采用末端限制性片段长度多态性分析比较溃疡性结肠炎和克罗恩病的粪便微生物菌群特征。
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7
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.全基因组荟萃分析将确认的克罗恩病易感性位点数量增加到 71 个。
Nat Genet. 2010 Dec;42(12):1118-25. doi: 10.1038/ng.717.
8
IL-1 family nomenclature.白细胞介素-1家族命名法。
Nat Immunol. 2010 Nov;11(11):973. doi: 10.1038/ni1110-973.
9
IL-37 is a fundamental inhibitor of innate immunity.白细胞介素 37 是先天免疫的基本抑制剂。
Nat Immunol. 2010 Nov;11(11):1014-22. doi: 10.1038/ni.1944. Epub 2010 Oct 10.
10
Interleukin-33 expression is specifically enhanced in inflamed mucosa of ulcerative colitis.白细胞介素-33 的表达在溃疡性结肠炎的炎症黏膜中特异性增强。
J Gastroenterol. 2010 Oct;45(10):999-1007. doi: 10.1007/s00535-010-0245-1. Epub 2010 Apr 20.

肠病性白细胞介素-37b 的上皮细胞表达。

Epithelial expression of interleukin-37b in inflammatory bowel disease.

机构信息

Department of Medicine, Shiga University of Medical Science, Otsu, Japan.

出版信息

Clin Exp Immunol. 2013 Jun;172(3):410-6. doi: 10.1111/cei.12061.

DOI:10.1111/cei.12061
PMID:23600829
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3646440/
Abstract

Interleukin (IL)-37 is a member of the IL-1 cytokine family. We investigated IL-37b expression in the inflamed mucosa of inflammatory bowel disease (IBD) patients. Furthermore, we analysed IL-37b expression in human colonic epithelial cells. The human colonic epithelial cell line T84 and human colonic subepithelial myofibroblasts (SEMFs) were used. IL-37b expression in the IBD mucosa was evaluated by immunohistochemistry. IL-37b mRNA and protein expression were determined by real time-polymerase chain reaction (PCR) and Western blotting, respectively. IL-37b was not detected in the normal colonic mucosa. In the inflamed mucosa of IBD patients, epithelial IL-37b expression was increased markedly. In ulcerative colitis (UC) and Crohn's disease (CD) patients, IL-37b expression was enhanced in the affected mucosa. In the intestinal epithelial cell line T84, the expression of IL-37b mRNA and protein was enhanced by tumour necrosis factor (TNF)-α. This IL-37b induction by TNF-α was mediated by nuclear factor (NF)-κB and activator protein (AP)-1 activation. Furthermore, IL-37b inhibited TNF-α-induced interferon-γ-inducible protein (IP)-10 expression significantly in human colonic SEMFs. Epithelial IL-37b expression was increased in IBD patients, especially UC patients. IL-37b may be involved in the pathophysiology of IBD as an anti-inflammatory cytokine and an inhibitor of both innate and acquired immune responses.

摘要

白细胞介素 (IL)-37 是 IL-1 细胞因子家族的一员。我们研究了炎症性肠病 (IBD) 患者炎症黏膜中 IL-37b 的表达。此外,我们还分析了人结肠上皮细胞中 IL-37b 的表达。使用人结肠上皮细胞系 T84 和人结肠黏膜下肌成纤维细胞 (SEMFs)。通过免疫组织化学评估 IBD 黏膜中 IL-37b 的表达。通过实时聚合酶链反应 (PCR) 和 Western blot 分别测定 IL-37b mRNA 和蛋白表达。在正常结肠黏膜中未检测到 IL-37b。在 IBD 患者的炎症黏膜中,上皮细胞 IL-37b 的表达明显增加。在溃疡性结肠炎 (UC) 和克罗恩病 (CD) 患者中,受影响的黏膜中 IL-37b 的表达增强。在肠上皮细胞系 T84 中,肿瘤坏死因子 (TNF)-α 增强了 IL-37b mRNA 和蛋白的表达。这种由 TNF-α 诱导的 IL-37b 表达是通过核因子 (NF)-κB 和激活蛋白 (AP)-1 激活介导的。此外,IL-37b 显著抑制 TNF-α 诱导的干扰素-γ 诱导蛋白 (IP)-10 在人结肠 SEMFs 中的表达。IBD 患者,尤其是 UC 患者,上皮细胞 IL-37b 的表达增加。IL-37b 可能作为抗炎细胞因子和先天和获得性免疫反应的抑制剂参与 IBD 的病理生理过程。