Chua Anita C G, Graham Ross M, Trinder Debbie, Olynyk John K
School of Medicine and Pharmacology, University of Western Australia, Fremantle, Western Australia, Australia.
Crit Rev Clin Lab Sci. 2007;44(5-6):413-59. doi: 10.1080/10408360701428257.
While iron is an essential trace element required by nearly all living organisms, deficiencies or excesses can lead to pathological conditions such as iron deficiency anemia or hemochromatosis, respectively. A decade has passed since the discovery of the hemochromatosis gene, HFE, and our understanding of hereditary hemochromatosis (HH) and iron metabolism in health and a variety of diseases has progressed considerably. Although HFE-related hemochromatosis is the most widespread, other forms of HH have subsequently been identified. These forms are not attributed to mutations in the HFE gene but rather to mutations in genes involved in the transport, storage, and regulation of iron. This review is an overview of cellular iron metabolism and regulation, describing the function of key proteins involved in these processes, with particular emphasis on the liver's role in iron homeostasis, as it is the main target of iron deposition in pathological iron overload. Current knowledge on their roles in maintaining iron homeostasis and how their dysregulation leads to the pathogenesis of HH are discussed.
铁是几乎所有生物所需的必需微量元素,但其缺乏或过量分别会导致诸如缺铁性贫血或血色素沉着症等病理状况。自血色素沉着症基因HFE被发现至今已有十年,我们对遗传性血色素沉着症(HH)以及健康和各种疾病状态下铁代谢的认识有了显著进展。尽管与HFE相关的血色素沉着症最为普遍,但随后又鉴定出了其他形式的HH。这些形式并非归因于HFE基因突变,而是由于参与铁运输、储存和调节的基因突变。本综述概述了细胞铁代谢和调节,描述了参与这些过程的关键蛋白质的功能,特别强调肝脏在铁稳态中的作用,因为它是病理性铁过载中铁沉积的主要靶点。本文还讨论了它们在维持铁稳态中的作用以及失调如何导致HH发病机制的当前知识。