Androulidaki Ariadne, Iliopoulos Dimitrios, Arranz Alicia, Doxaki Christina, Schworer Steffen, Zacharioudaki Vassiliki, Margioris Andrew N, Tsichlis Philip N, Tsatsanis Christos
Department of Clinical Chemistry, School of Medicine, University of Crete, Heraklion 71003, Crete, Greece.
Immunity. 2009 Aug 21;31(2):220-31. doi: 10.1016/j.immuni.2009.06.024.
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 LPS, 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 LPS in culture and in animals. These results indicate that Akt1 regulates the response of macrophages to LPS by controlling miRNA expression.
脂多糖(LPS)调控的微小RNA靶向有助于炎症表型的基因。在此,我们发现被LPS激活的蛋白激酶Akt1正向调控微小RNA let-7e和miR-181c,但负向调控miR-155和miR-125b。计算机分析和转染研究表明,let-7e抑制Toll样受体4(TLR4),而miR-155抑制SOCS1,这两种蛋白对LPS驱动的TLR信号传导至关重要,它们调节内毒素敏感性和耐受性。因此,Akt1基因敲除的巨噬细胞在培养中对LPS的反应性增强,且Akt1基因敲除小鼠在体内未形成内毒素耐受性。在Akt1基因敲除的巨噬细胞中过表达let-7e并抑制miR-155可恢复培养物和动物中对LPS的敏感性和耐受性。这些结果表明,Akt1通过控制微小RNA的表达来调节巨噬细胞对LPS的反应。