期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 286, 期 2, 页码 1436-1444出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M110.145870
关键词
-
资金
- National Institutes of Health [AA011576, AA008577]
- Alfonso Martin Escudero Foundation, Spain
- Diabetes Endocrinology Research Center [DK32520]
Activation of Kupffer cells (KCs) by gut-derived lipopolysaccharide (LPS) and Toll-Like Receptors 4 (TLR4)-LPS-mediated increase in TNF alpha production has a central role in the pathogenesis of alcoholic liver disease. Micro-RNA (miR)-125b, miR-146a, and miR-155 can regulate inflammatory responses to LPS. Here we evaluated the involvement of miRs in alcohol-induced macrophage activation. Chronic alcohol treatment in vitro resulted in a time-dependent increase in miR-155 but not miR-125b or miR-146a levels in RAW 264.7 macrophages. Furthermore, alcohol pretreatment augmented LPS-induced miR-155 expression in macrophages. We found a linear correlation between alcohol-induced increase in miR-155 and TNF alpha induction. In a mouse model of alcoholic liver disease, we found a significant increase in both miR-155 levels and TNF alpha production in isolated KCs when compared with pair-fed controls. The mechanistic role of miR-155 in TNF alpha regulation was indicated by decreased TNF alpha levels in alcohol-treated macrophages after inhibition of miR-155 and by increased TNF alpha production after miR-155 overexpression, respectively. We found that miR-155 affected TNF alpha mRNA stability because miR-155 inhibition decreased whereas miR-155 overexpression increased TNF alpha mRNA half-life. Using the NF-kappa B inhibitors, MG-132 or Bay11-7082, we demonstrated that NF-kappa B activation mediated the up-regulation of miR-155 by alcohol in KCs. In conclusion, our novel data demonstrate that chronic alcohol consumption increases miR-155 in macrophages via NF-kappa B and the increased miR-155 contributes to alcohol-induced elevation in TNF alpha production via increased mRNA stability.
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