Department of Biochemical Sciences, Sapienza University, Rome, Italy.
Department of Biosciences and Territory, University of Molise, C.da Fonte Lappone, 86090, Pesche, IS, Italy.
Biometals. 2018 Jun;31(3):399-414. doi: 10.1007/s10534-018-0087-5. Epub 2018 Feb 16.
In the last 20 years, several new genes and proteins involved in iron metabolism in eukaryotes, particularly related to pathological states both in animal models and in humans have been identified, and we are now starting to unveil at the molecular level the mechanisms of iron absorption, the regulation of iron transport and the homeostatic balancing processes. In this review, we will briefly outline the general scheme of iron metabolism in humans and then focus our attention on the cellular iron export system formed by the permease ferroportin and the ferroxidase ceruloplasmin. We will finally summarize data on the role of the iron binding protein lactoferrin on the regulation of the ferroportin/ceruloplasmin couple and of other proteins involved in iron homeostasis in inflamed human macrophages.
在过去的 20 年中,人们已经鉴定出几种涉及真核生物铁代谢的新基因和蛋白质,特别是与动物模型和人类病理状态相关的基因和蛋白质。我们现在开始从分子水平揭示铁吸收、铁转运调控和体内平衡平衡过程的机制。在这篇综述中,我们将简要概述人类铁代谢的一般方案,然后将注意力集中在由 permease ferroportin 和 ferroxidase ceruloplasmin 组成的细胞铁输出系统上。最后,我们将总结关于铁结合蛋白乳铁蛋白(lactoferrin)在调节铁稳态相关蛋白的作用的研究数据,包括炎症状态下人巨噬细胞中的 ferroportin/ceruloplasmin 偶联和其他铁稳态蛋白。