Human iron transporters

被引:44
作者
Garrick, Michael D. [1 ]
机构
[1] SUNY Buffalo, Dept Biochem, Buffalo, NY 14214 USA
关键词
Divalent metal transporter (DMT1); Ferroportin; Isoforms; Transferrin; Ferric reductase; Iron-responsive element (IRE); Iron regulatory protein (IRP); DIVALENT METAL TRANSPORTER-1; SUBCELLULAR-LOCALIZATION; CYTOSOLIC ACONITASE; RESPONSIVE ELEMENT; CHANNEL BLOCKERS; ERYTHROID-CELLS; DMT1; PROTEIN; H-FERRITIN; ISOFORMS; EXPRESSION;
D O I
10.1007/s12263-010-0184-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Human iron transporters manage iron carefully because tissues need iron for critical functions, but too much iron increases the risk of reactive oxygen species. Iron acquisition occurs in the duodenum via divalent metal transporter (DMT1) and ferroportin. Iron trafficking depends largely on the transferrin cycle. Nevertheless, non-digestive tissues have a variety of other iron transporters that may render DMT1 modestly redundant, and DMT1 levels exceed those needed for the just-mentioned tasks. This review begins to consider why and also describes advances after 2008 that begin to address this challenge.
引用
收藏
页码:45 / 54
页数:10
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