FEBS Letters
Volume 584, Issue 8 , Pages 1481-1486, 16 April 2010

Identification of MyD88 as a novel target of miR-155, involved in negative regulation of Helicobacter pylori-induced inflammation

  • Bin Tang

      Affiliations

    • Department of Clinical Microbiology and Immunology, College of Medical Laboratory Science, Third Military Medical University, Chongqing 400038, China
    • Emei Sanatorium of Chengdu Military Region, Emeishan, Sichuan 614205, China
    • Bin Tang and Bin Xiao contributed equally to this work.
  • ,
  • Bin Xiao

      Affiliations

    • Department of Clinical Microbiology and Immunology, College of Medical Laboratory Science, Third Military Medical University, Chongqing 400038, China
    • Bin Tang and Bin Xiao contributed equally to this work.
  • ,
  • Zhen Liu

      Affiliations

    • Department of Clinical Microbiology and Immunology, College of Medical Laboratory Science, Third Military Medical University, Chongqing 400038, China
  • ,
  • Na Li

      Affiliations

    • Department of Clinical Microbiology and Immunology, College of Medical Laboratory Science, Third Military Medical University, Chongqing 400038, China
  • ,
  • En-Dong Zhu

      Affiliations

    • Department of Clinical Microbiology and Immunology, College of Medical Laboratory Science, Third Military Medical University, Chongqing 400038, China
  • ,
  • Bo-Sheng Li

      Affiliations

    • Department of Clinical Microbiology and Immunology, College of Medical Laboratory Science, Third Military Medical University, Chongqing 400038, China
  • ,
  • Qing-Hua Xie

      Affiliations

    • Department of Clinical Microbiology and Immunology, College of Medical Laboratory Science, Third Military Medical University, Chongqing 400038, China
  • ,
  • Yuan Zhuang

      Affiliations

    • Department of Clinical Microbiology and Immunology, College of Medical Laboratory Science, Third Military Medical University, Chongqing 400038, China
  • ,
  • Quan-Ming Zou

      Affiliations

    • Department of Clinical Microbiology and Immunology, College of Medical Laboratory Science, Third Military Medical University, Chongqing 400038, China
    • Corresponding Author InformationCorresponding authors. Address: Department of Clinical Microbiology and Immunology, College of Medical Laboratory Science, Third Military Medical University, No. 30, Gaotanyan Street, Chongqing 400038, China. Fax: +86 023 68752316 (X.H. Mao).
  • ,
  • Xu-Hu Mao

      Affiliations

    • Department of Clinical Microbiology and Immunology, College of Medical Laboratory Science, Third Military Medical University, Chongqing 400038, China
    • Corresponding Author InformationCorresponding authors. Address: Department of Clinical Microbiology and Immunology, College of Medical Laboratory Science, Third Military Medical University, No. 30, Gaotanyan Street, Chongqing 400038, China. Fax: +86 023 68752316 (X.H. Mao).

Received 4 December 2009; received in revised form 6 February 2010; accepted 23 February 2010. published online 26 February 2010.

Edited by Tamas Dalmay

Abstract 

MicroRNA-155 (miR-155) has been implicated as a central regulator of the immune system. We have previously reported that miR-155 negatively regulates Helicobacter pylori (H. pylori)-induced inflammation, but the molecular mechanism of miR-155 regulating the inflammation is not fully clear. Here, we identified myeloid differentiation protein 88 (MyD88) as a target gene of miR-155, and found that miR-155 decreased MyD88 expression at the protein but not the mRNA message level, suggesting that the miR-155-mediated inhibition is a post-transcriptional event. Furthermore, the overexpression of miR-155 led to significantly reduced IL-8 production induced by H. pylori infection. Thus, we have demonstrated that miR-155 can negatively regulate inflammation by targeting a key adaptor molecule MyD88 in inflammatory pathways.

Keywords: MiR-155, MyD88, Inflammation, Helicobacter pylori

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PII: S0014-5793(10)00167-5

doi:10.1016/j.febslet.2010.02.063

FEBS Letters
Volume 584, Issue 8 , Pages 1481-1486, 16 April 2010