Peyssonnaux Carole, Nizet Victor, Johnson Randall S
Institut Cochin, Université Paris Descartes, CNRS (UMR 8104), Paris, France.
Cell Cycle. 2008 Jan 1;7(1):28-32. doi: 10.4161/cc.7.1.5145.
Iron is an essential element in all living organisms and is required as a cofactor for oxygen-binding proteins. Iron metabolism, oxygen homeostasis and erythropoiesis are consequently strongly interconnected. Iron needs to be tightly regulated, as iron insufficiency induces a hypoferric anemia in mammals, coupled to hypoxia in tissues, whereas excess iron is toxic, and causes generation of free radicals. Given the links between oxygen transport and iron metabolism, associations between the physiology of hypoxic response, and the control of iron availability are important. Numerous lines of investigation have proven that the HIF transcription factors function as central mediators of cellular adaptation to critically low oxygen levels in both normal and compromised tissues. Several of these target genes are involved in iron homeostasis, reflecting the molecular links between oxygen homeostasis and iron metabolism.
铁是所有生物体内的必需元素,作为氧结合蛋白的辅助因子发挥作用。因此,铁代谢、氧稳态和红细胞生成紧密相连。铁需要受到严格调控,因为铁缺乏会在哺乳动物中引发低铁性贫血,并伴有组织缺氧,而铁过量则有毒,会导致自由基的产生。鉴于氧运输与铁代谢之间的联系,低氧反应生理学与铁供应控制之间的关联十分重要。众多研究表明,HIF转录因子在正常组织和受损组织中均作为细胞适应严重低氧水平的核心介质发挥作用。其中一些靶基因参与铁稳态,反映了氧稳态与铁代谢之间的分子联系。