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miR-98 负向调控 LPS 刺激后巨噬细胞中 IL-10 的产生和内毒素耐受。

MicroRNA-98 negatively regulates IL-10 production and endotoxin tolerance in macrophages after LPS stimulation.

机构信息

Institute of Immunology, Zhejiang University School of Medicine, Hangzhou, China.

出版信息

FEBS Lett. 2011 Jun 23;585(12):1963-8. doi: 10.1016/j.febslet.2011.05.029. Epub 2011 May 20.

Abstract

Interleukin 10 (IL-10) is a potent anti-inflammatory cytokine that is crucial for dampening the inflammatory response after pathogen invasion, and was found to be produced by macrophages after exposure to lipopolysaccharide (LPS). It remains unclear whether microRNA-mediated regulatory mechanism is involved in LPS-induced IL-10 production. Here we reported that miR-98 expression in macrophages significantly decreased following LPS stimulation. We also found that miR-98 targets the 3'untranslated region of IL-10 transcript. Overexpression of miR-98 inhibited TLR4-triggered IL-10 production and promoted COX-2 expression. We further demonstrated that miR-98 significantly mitigated the induction of endotoxin tolerance, suggesting that miR-98-mediated posttranscriptional control could potentially be involved in fine tuning the critical level of IL-10 production in endotoxin tolerance.

摘要

白细胞介素 10(IL-10)是一种有效的抗炎细胞因子,对于在病原体入侵后抑制炎症反应至关重要,并且发现在巨噬细胞暴露于脂多糖(LPS)后会产生。目前尚不清楚是否涉及 microRNA 介导的调节机制在 LPS 诱导的 IL-10 产生中。在这里,我们报道了 LPS 刺激后巨噬细胞中 miR-98 的表达明显降低。我们还发现 miR-98 靶向 IL-10 转录本的 3'非翻译区。miR-98 的过表达抑制 TLR4 触发的 IL-10 产生并促进 COX-2 表达。我们进一步证明 miR-98 显著减轻了内毒素耐受的诱导,表明 miR-98 介导的转录后控制可能参与精细调节内毒素耐受中 IL-10 产生的关键水平。

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