School of Biochemistry & Immunology, Trinity College, Dublin, Ireland.
Nat Immunol. 2010 Feb;11(2):141-7. doi: 10.1038/ni.1828. Epub 2009 Nov 29.
The tumor suppressor PDCD4 is a proinflammatory protein that promotes activation of the transcription factor NF-kappaB 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-kappaB 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-kappaB. Transfection of cells with a miR-21 precursor blocked NF-kappaB 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.
肿瘤抑制因子 PDCD4 是一种促炎蛋白,可促进转录因子 NF-κB 的激活,并抑制白细胞介素 10(IL-10)的产生。在这里,我们发现缺乏 PDCD4 的小鼠可以免受脂多糖(LPS)诱导的死亡。LPS 诱导的 NF-κB 和 IL-6 需要 PDCD4,而 LPS 增强了缺乏 PDCD4 的细胞中 IL-10 的诱导。LPS 处理人外周血单核细胞导致 PDCD4 表达降低,这是由于衔接蛋白 MyD88 和 NF-κB 诱导 microRNA miR-21 的产生。用 miR-21 前体转染细胞可阻断 NF-κB 活性,并促进 LPS 诱导的 IL-10 产生,而用 miR-21 的反义寡核苷酸转染或靶向保护 Pdcd4 mRNA 中的 miR-21 位点则产生相反的效果。因此,miR-21 在 LPS 刺激后调节 PDCD4 的表达。