The Kinase Akt1 Controls Macrophage Response to Lipopolysaccharide by Regulating MicroRNAs

被引:526
|
作者
Androulidaki, Ariadne [1 ]
Iliopoulos, Dimitrios [3 ]
Arranz, Alicia [1 ]
Doxaki, Christina [1 ]
Schworer, Steffen [4 ]
Zacharioudaki, Vassiliki [1 ,2 ]
Margioris, Andrew N. [1 ]
Tsichlis, Philip N. [4 ]
Tsatsanis, Christos [1 ]
机构
[1] Univ Crete, Dept Clin Chem, Sch Med, Iraklion 71003, Crete, Greece
[2] Univ Crete, Grad Program Mol Basis Human Dis, Sch Med, Iraklion 71003, Crete, Greece
[3] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[4] Tufts Med Ctr, Mol Oncol Res Inst, Boston, MA 02111 USA
基金
美国国家卫生研究院;
关键词
SIGNALING PATHWAY; GENE-EXPRESSION; TOLL-LIKE-RECEPTOR-4; EXPRESSION; TRANSCRIPTION FACTORS; NEGATIVE REGULATION; CYTOKINE PRODUCTION; CELLS; ALPHA; MICE; LPS;
D O I
10.1016/j.immuni.2009.06.024
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
MicroRNAs regulated by lipopolysaccharide (LPS) target genes that contribute to the inflammatory phenotype. Here, we showed that the protein kinase Akt1, which is activated by LIPS, positively regulated miRNAs let-7e and miR-181c but negatively regulated miR-155 and miR-125b. In silico analyses and transfection studies revealed that let-7e repressed Toll-like receptor 4 (TLR4), whereas miR-155 repressed SOCS1, two proteins critical for LPS-driven TLR signaling, which regulate endotoxin sensitivity and tolerance. As a result, Akt1(-/-) macrophages exhibited increased responsiveness to LPS in culture and Akt1(-/-) mice did not develop endotoxin tolerance in vivo. Overexpression of let-7e and suppression of miR-155 in Akt1(-/-) macrophages restored sensitivity and tolerance to LIPS in culture and in animals. These results indicate that Akt1 regulates the response of macrophages to LPS by controlling miRNA expression.
引用
收藏
页码:220 / 231
页数:12
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