IL-10 Inhibits miR-155 Induction by Toll-like Receptors

被引:211
作者
McCoy, Claire E. [1 ]
Sheedy, Frederick J. [1 ]
Qualls, Joseph E. [2 ]
Doyle, Sarah L. [1 ]
Quinn, Susan R. [1 ]
Murray, Peter J. [2 ]
O'Neill, Luke A. J. [1 ]
机构
[1] Univ Dublin Trinity Coll, Sch Biochem & Immunol, Dublin 2, Ireland
[2] St Jude Childrens Hosp, Dept Infect Dis, Memphis, TN 38105 USA
基金
爱尔兰科学基金会;
关键词
DOMAIN-CONTAINING INOSITOL-5-PHOSPHATASE; B-CELL LYMPHOMAS; IMMUNE-RESPONSE; TRANSGENIC MICE; EXPRESSION; MICRORNA; TARGET; TRANSCRIPTION; ACTIVATION; PATHWAY;
D O I
10.1074/jbc.M110.102111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
IL-10 is a potent anti-inflammatory cytokine that is crucial for down-regulating pro-inflammatory genes, which are induced by Toll-like receptor (TLR) signaling. In this study, we have examined whether modulation of microRNAs plays a role in the inhibitory effect of IL-10 on TLR4 signaling. Analyzing microRNAs known to be induced by TLR4, we found that IL-10 could inhibit the expression of miR-155 in response to lipopolysaccharide but had no effect on miR-21 or miR-146a. IL-10 inhibited miR-155 transcription from the BIC gene in a STAT3-dependent manner. This inhibitory effect of IL-10 on miR-155 led to an increase in the expression of the miR-155 target, SHIP1. This is the first example of IL-10 playing a role in microRNA function and suggests that through its inhibitory effect on miR-155, IL-10 has the ability to promote anti-inflammatory gene expression.
引用
收藏
页码:20492 / 20498
页数:7
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