Differential expression of interleukin-1/Toll-like receptor signaling regulators in microscopic and ulcerative colitis

被引:54
作者
Gunaltay, Sezin [1 ]
Nyhlin, Nils [2 ]
Kumawat, Ashok Kumar [1 ]
Tysk, Curt [2 ]
Bohr, Johan [2 ]
Hultgren, Olof [3 ]
Hornquist, Elisabeth Hultgren [1 ]
机构
[1] Univ Orebro, Sch Hlth & Med Sci, Dept Biomed, SE-70182 Orebro, Sweden
[2] Univ Orebro, Orebro Univ Hosp, Sch Hlth & Med Sci, Dept Med,Div Gastroenterol, SE-70185 Orebro, Sweden
[3] Orebro Univ Hosp, Dept Microbiol & Immunol, SE-70185 Orebro, Sweden
关键词
Interleukin-37; MicroRNA; Lymphocytic colitis; Collagenous colitis; Ulcerative colitis; NF-KAPPA-B; IRAK-M; COLLAGENOUS COLITIS; LYMPHOCYTIC COLITIS; NEGATIVE REGULATOR; INNATE IMMUNITY; CROHNS-DISEASE; MICRORNAS; RESPONSES; CYTOKINE;
D O I
10.3748/wjg.v20.i34.12249
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
AIM: To investigate Toll-like receptor (TLR) signaling regulators in microscopic and ulcerative colitis patients. METHODS: Total RNA and microRNA were isolated from fresh frozen colonic biopsies of non-inflamed controls and patients with active or in-remission collagenous colitis (CC), lymphocytic colitis (LC), or ulcerative colitis (UC). We compared expressions of interleukin-1 receptor-associated kinase (IRAK)-2, IRAK-M, interleukin (IL)-37, microRNA (miR)-146a, miR-155, and miR-21 using quantitative real time reverse transcription polymerase chain reaction. RESULTS: IRAK-M expression was increased in LC patients with active disease in histopathological remission (LC-HR; P = 0.02) and UC patients (P = 0.01), but no differences in IRAK-2 expression were detected compared to controls. miR-146a, -155 and -21 expressions were increased in LC-HR (P = 0.04, 0.07, and 0.004) and UC (P = 0.02, 0.04 and 0.03) patients. miR-146a and miR-21 expressions were significantly enhanced in UC patients compared to UC remission (UC-R; P = 0.01 and 0.04). Likewise, active CC patients showed significantly increased expression of miR-155 (P = 0.003) and miR-21 (P = 0.006). IL-37 expression was decreased in both CC (P = 0.03) and LC (P = 0.04) patients with a similar trend in UC patients but not statistically significant, whilst it was increased in UC-R patients compared to controls (P = 0.02) and active UC (P = 0.001). CONCLUSION: The identification of differentially expressed miRNAs, IL-37, and IRAK-M suggests different pathophysiologic mechanisms in various disease stages in LC, CC, and UC. (C) 2014 Baishideng Publishing Group Inc. All rights reserved.
引用
收藏
页码:12249 / 12259
页数:11
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