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人体铁代谢。

Iron metabolism in man.

机构信息

University of California, Medical Offices South, 200 West Arbor Drive, #8651, San Diego, CA 92103-8651, USA.

出版信息

JPEN J Parenter Enteral Nutr. 2013 Sep;37(5):599-606. doi: 10.1177/0148607112459648. Epub 2012 Sep 11.

Abstract

Iron metabolism in man is a highly regulated process designed to provide iron for erythropoiesis, mitochondrial energy production, electron transport, and cell proliferation. The mechanisms of iron handling also protect cells from the deleterious effects of free iron, which can produce oxidative damage of membranes, proteins, and lipids. Over the past decade, several important molecules involved in iron homeostasis have been discovered, and their function has expanded our understanding of iron trafficking under normal and pathological conditions. Physiologic iron metabolism is strongly influenced by inflammation, which clinically leads to anemia. Although hepcidin, a small circulating peptide produced by the liver, has been found to be the key regulator of iron trafficking, molecular pathways of iron sensing that control iron metabolism and hepcidin production are still incompletely understood. With this review, we provide an overview of the current understanding of iron metabolism, the recently discovered regulators of iron trafficking, and a focus on the effects of inflammation on the process.

摘要

人体内的铁代谢是一个高度调节的过程,旨在为红细胞生成、线粒体能量产生、电子传递和细胞增殖提供铁。铁处理的机制还可以保护细胞免受游离铁的有害影响,游离铁会导致膜、蛋白质和脂质的氧化损伤。在过去的十年中,已经发现了几个参与铁稳态的重要分子,它们的功能扩展了我们对正常和病理条件下铁运输的理解。生理铁代谢受炎症的强烈影响,这在临床上会导致贫血。尽管肝脏产生的小循环肽——铁调素已被发现是铁运输的关键调节剂,但控制铁代谢和铁调素产生的铁感应分子途径仍不完全清楚。通过这篇综述,我们概述了目前对铁代谢的理解、最近发现的铁运输调节剂,以及炎症对该过程的影响。

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