Identification of MyD88 as a novel target of miR‐155, involved in negative regulation of <i>Helicobacter pylori</i>‐induced inflammation

Bin Tang(Army Medical University), Bin Xiao(Army Medical University), Zhen Liu(Army Medical University), Na Li(Army Medical University), Endong Zhu(Army Medical University), Bo–Sheng Li(Army Medical University), Qing‐Hua Xie(Army Medical University), Yuan Zhuang(Army Medical University), Quanming Zou(Army Medical University), Xuhu Mao(Army Medical University)
FEBS Letters
February 26, 2010
Cited by 201

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.


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