Iron uptake and metabolism in the new millennium.

Trends Cell Biol

Iron Metabolism and Chelation Program, Department of Pathology, Blackburn Building D06, University of Sydney, Sydney, NSW 2006, Australia.

Published: February 2007

AI Article Synopsis

  • Iron is crucial for life but can be harmful if not properly regulated, leading to iron homeostasis through transport, storage, and regulatory proteins.
  • Some well-known proteins like transferrin and its receptor are understood, while the function of others, like melanotransferrin, is still unclear.
  • Recent years have revealed new molecules involved in iron metabolism, including divalent metal transporter-1 and hepcidin, shedding light on cellular iron uptake and regulation.

Article Abstract

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.

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Source
http://dx.doi.org/10.1016/j.tcb.2006.12.003DOI Listing

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