Induction of microRNA-155 during Helicobacter pylori Infection and Its Negative Regulatory Role in the Inflammatory Response

被引:238
|
作者
Xiao, Bin [1 ]
Liu, Zhen [1 ,4 ]
Li, Bo-Sheng [1 ]
Tang, Bin [1 ]
Li, Wei [2 ]
Guo, Gang [1 ]
Shi, Yun [1 ]
Wang, Fengjun [2 ]
Wu, Yuan [1 ]
Tong, Wen-De [1 ]
Guo, Hong [3 ]
Mao, Xu-Hu [1 ]
Zou, Quan-Ming [1 ]
机构
[1] Third Mil Med Univ, Dept Clin Microbiol & Immunol, Coll Med Lab Sci, Chongqing 400038, Peoples R China
[2] Third Mil Med Univ, Southwest Hosp, Chongqing 400038, Peoples R China
[3] Third Mil Med Univ, Dept Gastroenterol, Xinqiao Hosp, Chongqing 400038, Peoples R China
[4] Peoples Liberat Army Gen Hosp, Inst TB Res, Affiliated Hosp 2, Beijing, Peoples R China
来源
JOURNAL OF INFECTIOUS DISEASES | 2009年 / 200卷 / 06期
基金
中国国家自然科学基金;
关键词
NF-KAPPA-B; EXPRESSION; MIR-155; GENE; RNA; CONTRIBUTES; MODULATION; IMMUNITY; PATHWAY; HODGKIN;
D O I
10.1086/605443
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. MicroRNAs (miRNAs) are small, noncoding RNAs that regulate gene expression at posttranscriptional level. H. pylori is a major human pathogenic bacterium in gastric mucosa. To date, the role of miRNAs in response to H. pylori infection has not been explored. Methods. The expression profile of cellular miRNAs during H. pylori infection was analyzed by using microarray and quantitative reverse-transcriptase polymerase chain reaction. The potential target of miR-155 was identified by luciferase assay and Western blot. Promoter analysis and inhibitor experiment were used to investigate the pathway involved in the induction of miR-155. Examination of miR-155 function was performed by overexpression and inhibition of miR-155. Results. H. pylori was able to increase the miR-155 expression in gastric epithelial cell lines and gastric mucosal tissues, and nuclear factor-kappa B (NF-kappa B) and activator protein-1 (AP-1) pathway were required for the induction of miR-155. miR-155 may down-regulate I kappa B kinase epsilon, Sma- and Mad-related protein 2 (SMAD2), and Fas-associated death domain protein. Furthermore, the overexpression of miR-155 negatively regulated the release of interleukin-8 and growth-related oncogene-alpha. Conclusions. This study provides the first description of increased expression of miR-155 in H. pylori infection, and miR-155 may function as novel negative regulator that help to fine-tune the inflammation response of H. pylori infection.
引用
收藏
页码:916 / 925
页数:10
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