Guo Zhen, Wu Rong, Gong Jianfeng, Zhu Weiming, Li Yi, Wang Zhiming, Li Ning, Li Jieshou
Department of General Surgery, Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
J Gastroenterol Hepatol. 2015 Jan;30(1):109-16. doi: 10.1111/jgh.12644.
MicroRNAs (miRNAs) play an important role in inflammation. Several studies have reported the unique miRNA profiles in colonic mucosa and peripheral blood of patients with active Crohn's disease (CD). But there is limited data about the miRNA profiles of the terminal ileum, the most commonly involved location, especially the non-inflamed mucosa. We aimed to investigate the miRNA expression of both inflamed and non-inflamed terminal ileal mucosa in adult patients with active CD.
Total RNA of all mucosal samples was extracted. MiRNA expression profile was assessed using microarray technology, and then selected miRNAs were evaluated using quantitative reverse-transcription polymerase chain reaction (qRT-PCR) to confirm the results of the microarray investigation.
Sixteen CD patients and 10 healthy adults were included. Samples of six patients and six controls were used for the microarray analysis. Samples of all participants were used for the validation of qRT-PCR. Results of the microarray showed miRNA expressions of both inflamed and non-inflamed mucosa were altered compared with controls. The differential expressions of hsa-miR-192-5p, hsa-miR-495-5p, hsa-let-7b-5p, hsa-miR-361-3p, and hsa-miR-124-3p were confirmed by qRT-PCR.
Both inflamed and non-inflamed terminal ileal mucosa in adult patients with active CD have their distinct miRNA expression patterns compared with healthy controls. Dysregulated miRNAs may be responsible for pathogenesis of CD.
微小RNA(miRNA)在炎症中起重要作用。多项研究报道了活动期克罗恩病(CD)患者结肠黏膜和外周血中独特的miRNA谱。但关于最常受累部位末端回肠,尤其是非炎症黏膜的miRNA谱的数据有限。我们旨在研究成年活动期CD患者炎症和非炎症末端回肠黏膜的miRNA表达。
提取所有黏膜样本的总RNA。使用微阵列技术评估miRNA表达谱,然后使用定量逆转录聚合酶链反应(qRT-PCR)评估所选miRNA以确认微阵列研究结果。
纳入16例CD患者和10名健康成年人。6例患者和6例对照的样本用于微阵列分析。所有参与者的样本用于qRT-PCR验证。微阵列结果显示,与对照相比,炎症和非炎症黏膜的miRNA表达均发生改变。qRT-PCR证实了hsa-miR-192-5p、hsa-miR-495-5p、hsa-let-7b-5p、hsa-miR-361-3p和hsa-miR-124-3p的差异表达。
与健康对照相比,成年活动期CD患者炎症和非炎症末端回肠黏膜均有其独特的miRNA表达模式。失调的miRNA可能与CD的发病机制有关。