Dunn Louise L, Suryo Rahmanto Yohan, Richardson Des R
Iron Metabolism and Chelation Program, Department of Pathology, Blackburn Building D06, University of Sydney, Sydney, NSW 2006, Australia.
Trends Cell Biol. 2007 Feb;17(2):93-100. doi: 10.1016/j.tcb.2006.12.003. Epub 2006 Dec 27.
Iron is an essential element for metabolic processes intrinsic to life, and yet the properties that make iron a necessity also make it potentially deleterious. To avoid harm, iron homeostasis is achieved through iron transport, storage and regulatory proteins. The functions of some of these molecules are well described, for example transferrin and transferrin receptor-1, whereas the roles of others, such as the transferrin homolog melanotransferrin, remain unclear. The past decade has seen the identification of new molecules involved in iron metabolism, such as divalent metal transporter-1, ferroportin-1, hepcidin, hemojuvelin and heme carrier protein-1. Here, we focus on these intriguing new molecules and the insights gained from them into cellular iron uptake and the regulation of iron metabolism.
铁是生命内在代谢过程所必需的元素,然而,使铁成为必需元素的特性也使其具有潜在危害。为避免危害,通过铁转运、储存和调节蛋白实现铁稳态。其中一些分子的功能已得到充分描述,例如转铁蛋白和转铁蛋白受体 -1,而其他分子的作用,如转铁蛋白同源物黑素转铁蛋白,仍不清楚。在过去十年中,已鉴定出参与铁代谢的新分子,如二价金属转运体 -1、铁转运蛋白 -1、铁调素、血色素沉着症相关蛋白和血红素载体蛋白 -1。在这里,我们重点关注这些有趣的新分子以及从它们身上获得的关于细胞铁摄取和铁代谢调节的见解。