On Iron Metabolism and Its Regulation

被引:316
作者
Vogt, Anne-Cathrine S. [1 ]
Arsiwala, Tasneem [1 ]
Mohsen, Mona [1 ,2 ]
Vogel, Monique [1 ]
Manolova, Vania [3 ]
Bachmann, Martin F. [1 ,4 ]
机构
[1] Univ Hosp Bern, Inselspital, Dept Rheumatol Immunol & Allergol, CH-3010 Bern, Switzerland
[2] Natl Ctr Canc Care & Res NCCCR, Doha 3050, Qatar
[3] Vifor Int AG, CH-9001 St Gallen, Switzerland
[4] Univ Oxford, Jenner Inst, Nuffield Dept Med, Oxford OX3 7BN, England
基金
瑞士国家科学基金会;
关键词
iron; macrophages; hepcidin; RED-BLOOD-CELLS; KUPFFER CELLS; HUMAN SPLEEN; MACROPHAGES; HOMEOSTASIS; HEPCIDIN; TRAFFICKING; LIVER; DIFFERENTIATION; MONOCYTES;
D O I
10.3390/ijms22094591
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 a critical metal for several vital biological processes. Most of the body's iron is bound to hemoglobin in erythrocytes. Iron from senescent red blood cells is recycled by macrophages in the spleen, liver and bone marrow. Dietary iron is taken up by the divalent metal transporter 1 (DMT1) in enterocytes and transported to portal blood via ferroportin (FPN), where it is bound to transferrin and taken up by hepatocytes, macrophages and bone marrow cells via transferrin receptor 1 (TfR1). While most of the physiologically active iron is bound hemoglobin, the major storage of most iron occurs in the liver in a ferritin-bound fashion. In response to an increased iron load, hepatocytes secrete the peptide hormone hepcidin, which binds to and induces internalization and degradation of the iron transporter FPN, thus controlling the amount of iron released from the cells into the blood. This review summarizes the key mechanisms and players involved in cellular and systemic iron regulation.
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页数:17
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