Negative regulation of TLR4 via targeting of the proinflammatory tumor suppressor PDCD4 by the microRNA miR-21

被引:826
作者
Sheedy, Frederick J. [1 ]
Palsson-McDermott, Eva [1 ]
Hennessy, Elizabeth J. [1 ]
Martin, Cara [2 ,3 ]
O'Leary, John J. [2 ,3 ]
Ruan, Qingguo [4 ]
Johnson, Derek S. [4 ]
Chen, Youhai [4 ]
O'Neill, Luke A. J. [1 ]
机构
[1] Trinity Coll Dublin, Sch Biochem & Immunol, Dublin, Ireland
[2] Coombe Womens Hosp, Dept Pathol, Dublin, Ireland
[3] Trinity Coll Dublin, Sch Med, Dept Histopathol, Dublin, Ireland
[4] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
基金
爱尔兰科学基金会;
关键词
NF-KAPPA-B; INITIATION-FACTOR; 4E; PROGRAMMED CELL-DEATH-4; IMMUNE-RESPONSES; GENE-EXPRESSION; TRANSLATION INITIATION; AP-1; TRANSACTIVATION; SPLICE VARIANT; MESSENGER-RNA; CELLS;
D O I
10.1038/ni.1828
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The tumor suppressor PDCD4 is a proinflammatory protein that promotes activation of the transcription factor NF-kappa B and suppresses interleukin 10 (IL-10). Here we found that mice deficient in PDCD4 were protected from lipopolysaccharide (LPS)-induced death. The induction of NF-kappa B and IL-6 by LPS required PDCD4, whereas LPS enhanced IL-10 induction in cells lacking PDCD4. Treatment of human peripheral blood mononuclear cells with LPS resulted in lower PDCD4 expression, which was due to induction of the microRNA miR-21 via the adaptor MyD88 and NF-kappa B. Transfection of cells with a miR-21 precursor blocked NF-kappa B activity and promoted IL-10 production in response to LPS, whereas transfection with antisense oligonucleotides to miR-21 or targeted protection of the miR-21 site in Pdcd4 mRNA had the opposite effect. Thus, miR-21 regulates PDCD4 expression after LPS stimulation.
引用
收藏
页码:141 / U59
页数:8
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