Regulation of cellular iron metabolism

被引:745
作者
Wang, Jian [1 ,2 ]
Pantopoulos, Kostas [1 ,2 ,3 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Biochem, Dallas, TX 75390 USA
[2] Sir Mortimer B Davis Jewish Hosp, Lady Davis Inst Med Res, Montreal, PQ H3T 1E2, Canada
[3] McGill Univ, Dept Med, Montreal, PQ H3A 1A3, Canada
关键词
ferritin; ferroportin; iron-regulatory protein 1 (IRP1); iron-regulatory protein 2 (IRP2); iron-sulfur cluster (ISC); transferrin receptor (TfR); AMYLOID PRECURSOR PROTEIN; TRANSFERRIN-BOUND IRON; HEPCIDIN EXPRESSION; OXIDATIVE STRESS; MAMMALIAN IRON; RESPONSIVE ELEMENT; RNA-BINDING; H-FERRITIN; MITOCHONDRIAL IRON; HEME-SYNTHESIS;
D O I
10.1042/BJ20101825
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
Iron is an essential but potentially hazardous biometal. Mammalian cells require sufficient amounts of iron to satisfy metabolic needs or to accomplish specialized functions. Iron is delivered to tissues by circulating transferrin, a transporter that captures iron released into the plasma mainly from intestinal enterocytes or reticuloendothelial macrophages. The binding of iron-laden transferrin to the cell-surface transferrin receptor 1 results in endocytosis and uptake of the metal cargo. Internalized iron is transported to mitochondria for the synthesis of haem or iron-sulfur clusters, which are integral parts of several metalloproteins, and excess iron is stored and detoxified in cytosolic ferritin. Iron metabolism is controlled at different levels and by diverse mechanisms. The present review summarizes basic concepts of iron transport, use and storage and focuses on the IRE (iron-responsive element)/IRP (iron-regulatory protein) system, a well known post-transcriptional regulatory circuit that not only maintains iron homoeostasis in various cell types, but also contributes to systemic iron balance.
引用
收藏
页码:365 / 381
页数:17
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