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microRNA‐210 negatively regulates LPS‐induced production of proinflammatory cytokines by targeting NF‐κB1 in murine macrophages
Author(s) -
Qi Jianni,
Qiao Yu,
Wang Peng,
Li Shuqing,
Zhao Wei,
Gao Chengjiang
Publication year - 2012
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/j.febslet.2012.03.011
Subject(s) - proinflammatory cytokine , tlr4 , lipopolysaccharide , transfection , regulator , inflammation , microrna , downregulation and upregulation , immunology , chemistry , microbiology and biotechnology , biology , biochemistry , gene
Ligation of TLR4 with LPS in macrophages leads to the production of proinflammatory cytokines, which are central to eliminate viral and bacterial infection. However, uncontrolled TLR4 activation may contribute to pathogenesis of inflammatory diseases such as septic shock. In this study, we found microRNA‐210 was induced in murine macrophages by LPS. Transfection of miR‐210 mimics significantly inhibited LPS‐induced production of inflammatory cytokines. In contrast, transfection of anti‐miR‐210 inhibitors increased LPS‐induced expression of proinflammatory cytokines. Furthermore, we demonstrated that miR‐210 targets NF‐κB1. Therefore, our data identify miR‐210 as a very important feedback negative regulator for LPS‐induced production of proinflammatory cytokines.
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