Mechanisms of Mammalian Iron Homeostasis

被引:482
作者
Pantopoulos, Kostas [3 ,4 ]
Porwal, Suheel Kumar [1 ]
Tartakoe, Alan [2 ]
Devireddy, L. [1 ]
机构
[1] Case Western Reserve Univ, Case Comprehens Canc Ctr, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
[3] McGill Univ, Jewish Gen Hosp, Lady Davis Inst Med Res, Montreal, PQ H3T 1E2, Canada
[4] McGill Univ, Dept Med, Montreal, PQ, Canada
基金
美国国家卫生研究院;
关键词
TRANSFERRIN RECEPTOR 2; HEREDITARY HEMOCHROMATOSIS PROTEIN; HEPCIDIN MESSENGER-RNA; REGULATORY PROTEIN-2; MICROCYTIC ANEMIA; CELLULAR IRON; ANTIMICROBIAL PEPTIDE; BOUND IRON; ERYTHROPOIETIC PROTOPORPHYRIA; MATRIPTASE-2; TMPRSS6;
D O I
10.1021/bi300752r
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 vital for almost all organisms because of its ability to donate and accept electrons with relative ease. It serves as a cofactor for many proteins and enzymes necessary for oxygen and energy metabolism, as well as for several other essential processes. Mammalian cells utilize multiple mechanisms to acquire iron. Disruption of iron homeostasis is associated with various human diseases: iron deficiency resulting from defects in the acquisition or distribution of the metal causes anemia, whereas iron surfeit resulting from excessive iron absorption or defective utilization causes abnormal tissue iron deposition, leading to oxidative damage. Mammals utilize distinct mechanisms to regulate iron homeostasis at the systemic and cellular levels. These involve the hormone hepcidin and iron regulatory proteins, which collectively ensure iron balance. This review outlines recent advances in iron regulatory pathways as well as in mechanisms underlying intracellular iron trafficking, an important but less studied area of mammalian iron homeostasis.
引用
收藏
页码:5705 / 5724
页数:20
相关论文
共 218 条
[1]   Transferrin receptor 1 [J].
Aisen, P .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2004, 36 (11) :2137-2143
[2]  
Aisen P, 1998, MET IONS BIOL SYST, V35, P585
[3]   Biosynthesis of heme in mammals [J].
Ajioka, Richard S. ;
Phillips, John D. ;
Kushner, James P. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2006, 1763 (07) :723-736
[4]   Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A) [J].
Allikmets, R ;
Raskind, WH ;
Hutchinson, A ;
Schueck, ND ;
Dean, M ;
Koeller, DM .
HUMAN MOLECULAR GENETICS, 1999, 8 (05) :743-749
[5]   Iron homeostasis: Insights from genetics and animal models [J].
Andrews, NC .
NATURE REVIEWS GENETICS, 2000, 1 (03) :208-217
[6]   BMP6 is a key endogenous regulator of hepcidin expression and iron metabolism [J].
Andriopoulos, Billy, Jr. ;
Corradini, Elena ;
Xia, Yin ;
Faasse, Sarah A. ;
Chen, Shanzhuo ;
Grgurevic, Lovorka ;
Knutson, Mitchell D. ;
Pietrangelo, Antonello ;
Vukicevic, Slobodan ;
Lin, Herbert Y. ;
Babitt, Jodie L. .
NATURE GENETICS, 2009, 41 (04) :482-487
[7]  
Arosio P., 2006, BIOCHIM BIOPHYS ACTA, V1790, P589
[8]   Cytosolic and mitochondrial ferritins in the regulation of cellular iron homeostasis and oxidative damage [J].
Arosio, Paolo ;
Levi, Sonia .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2010, 1800 (08) :783-792
[9]   Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression [J].
Babitt, JL ;
Huang, FW ;
Wrighting, DM ;
Xia, Y ;
Sidis, Y ;
Samad, TA ;
Campagna, JA ;
Chung, RT ;
Schneyer, AL ;
Woolf, CJ ;
Andrews, NC ;
Lin, HY .
NATURE GENETICS, 2006, 38 (05) :531-539
[10]   Modulation of bone morphogenetic protein signaling in vivo regulates systemic iron balance [J].
Babitt, Jodie L. ;
Huang, Franklin W. ;
Xia, Yin ;
Sidis, Yisrael ;
Andrews, Nancy C. ;
Lin, Herbert Y. .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (07) :1933-1939