Dual regulation of macrophage migration inhibitory factor (MIF) expression in hypoxia by CREB and HIF-1

被引:129
作者
Baugh, John A. [1 ]
Gantier, Michael [1 ]
Li, Lili [1 ]
Byrne, Aileen [1 ]
Buckley, Avril [1 ]
Donnelly, Seamas C. [1 ]
机构
[1] Univ Coll Dublin, Sch Med & Med Sci, Conway Inst Biomol & Biomed Res, Dublin 4, Ireland
基金
爱尔兰科学基金会;
关键词
macrophage migration inhibitory factor (MIF); hypoxia; inflammation; HIF-1; alpha; CREB;
D O I
10.1016/j.bbrc.2006.06.148
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Macrophage migration inhibitory factor (MIF) is a well-described pro-inflammatory mediator that has also been implicated in the process of oncogenic transformation and tumor progression. However, despite the compelling evidence that MIF is overexpressed in, and contributes to, the pathology of inflammatory and malignant diseases the mechanisms that contribute to exaggerated expression of MIF have been poorly described. Here we show that hypoxia, and specifically HIF-1 alpha, is a potent and rapid inducer of MIF expression. In addition, we demonstrate that hypoxia-induced MIF expression is dependent upon a HRE in the 5'UTR of the MIF gene but is further modulated by CREB expression. We propose a model where hypoxia-induced MIF expression is driven by HIF-1 but amplified by hypoxia-induced degradation of CREB. Given the importance of MIF in inflammatory and malignant diseases these data reveal a HIF-1-mediated pathway as a potential therapeutic target for suppression of MIF expression in hypoxic tissues. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:895 / 903
页数:9
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