MicroRNAs modulate the noncanonical transcription factor NF-κB pathway by regulating expression of the kinase IKKα during macrophage differentiation

被引:292
作者
Li, Tao [2 ]
Morgan, Michael J. [2 ]
Choksi, Swati [2 ]
Zhang, Yan [2 ]
Kim, You-Sun [1 ]
Liu, Zheng-gang [2 ]
机构
[1] Ajou Univ, Sch Med, Inst Med Sci, Suwon 441749, South Korea
[2] NCI, Cell & Canc Biol Branch, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
CONTROLS PROSTATE-CANCER; GENE-EXPRESSION; ACTIVATION; P100; INFLAMMATION; RECOGNITION; NF-KAPPA-B2; GENERATION; SURVIVAL; BIOLOGY;
D O I
10.1038/ni.1918
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 are key regulators of many biological processes including cell differentiation. Here we show that during human monocyte-macrophage differentiation expression of the microRNAs miR-223 miR-15a and miR-16 decreased considerably which led to higher expression of the serine-threonine kinase IKK alpha in macrophages. In macrophages higher IKK alpha expression in conjunction with stabilization of the kinase NIK induced larger amounts of p52. Because of low expression of the transcription factor ReIB in untreated macrophages high p52 expression repressed basal transcription of both canonical and noncanonical NF-kappa B target genes. However proinflammatory stimuli in macrophages resulted in greater induction of noncanonical NF-kappa B target genes. Thus a decrease in certain microRNAs probably prevents macrophage hyperactivation yet primes the macrophage for certain responses to proinflammatory stimuli.
引用
收藏
页码:799 / U48
页数:8
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