Two to Tango: Regulation of Mammalian Iron Metabolism

被引:1636
作者
Hentze, Matthias W. [1 ,2 ,3 ]
Muckenthaler, Martina U. [2 ,3 ,4 ]
Galy, Bruno [1 ]
Camaschella, Clara [5 ,6 ]
机构
[1] European Mol Biol Lab, D-69117 Heidelberg, Germany
[2] European Mol Biol Lab, Mol Med Partnership Unit, D-69120 Heidelberg, Germany
[3] Heidelberg Univ, D-69120 Heidelberg, Germany
[4] Dept Pediat Oncol Hematol & Immunol, D-69120 Heidelberg, Germany
[5] Ist Sci San Raffaele, Div Genet & Cell Biol, I-20132 Milan, Italy
[6] Univ Vita Salute San Raffaele, I-20132 Milan, Italy
关键词
HEREDITARY HEMOCHROMATOSIS PROTEIN; HEPCIDIN EXPRESSION; MOLECULAR-BASIS; MICROCYTIC ANEMIA; CHANNELS PROVIDE; MOUSE MODEL; CELL; TRANSFERRIN; RECEPTOR; HOMEOSTASIS;
D O I
10.1016/j.cell.2010.06.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Disruptions in iron homeostasis from both iron deficiency and overload account for some of the most common human diseases. Iron metabolism is balanced by two regulatory systems, one that functions systemically and relies on the hormone hepcidin and the iron exporter ferroportin, and another that predominantly controls cellular iron metabolism through iron-regulatory proteins that bind iron-responsive elements in regulated messenger RNAs. We describe how the two distinct systems function and how they tango" together in a coordinated manner. We also highlight some of the current questions in mammalian iron metabolism and discuss therapeutic opportunities arising from a better understanding of the underlying biological principles. © 2010 Elsevier Inc."
引用
收藏
页码:24 / 38
页数:15
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