Hepcidin: Iron-hormone and anti-microbial peptide

被引:78
作者
Falzacappa, MVV [1 ]
Muckenthaler, MU [1 ]
机构
[1] Heidelberg Univ, Dept Pediat Oncol Hematol & Immunol, D-69120 Heidelberg, Germany
关键词
hepcidin; iron metabolism; hereditary hemochromatosis; anaemia of chronic diseases; anti-microbial peptide;
D O I
10.1016/j.gene.2005.07.020
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Hepcidin is a beta-defensin-like peptide and a principle regulator of systemic iron homeostasis. In concordance with this dual function its expression is modulated by systemic iron requirements and in response to infectious and inflammatory stimuli. Studies of hepcidin provide novel insight into the molecular mechanisms involved in maintaining iron homeostasis in the healthy state and iron redistribution in response to chronic infections and inflammation. Furthermore, a deregulation of hepcidin may cause elevated intestinal iron absorption that hallmarks a group of frequent iron overload disorders, the Hereditary Hemochromatosis. The aim of this review is to discuss hepcidin function in iron-homeostasis under normal physiological and pathophysiological conditions. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:37 / 44
页数:8
相关论文
共 46 条
[1]   Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis [J].
Bridle, KR ;
Frazer, DM ;
Wilkins, SJ ;
Dixon, JL ;
Purdie, DM ;
Crawford, DHG ;
Subramaniam, VN ;
Powell, LW ;
Anderson, GJ ;
Ramm, GA .
LANCET, 2003, 361 (9358) :669-673
[2]   Juvenile and adult hemochromatosis are distinct genetic disorders [J].
Camaschella, C ;
Roetto, A ;
Cicilano, M ;
Pasquero, P ;
Bosio, S ;
Gubetta, L ;
Di Vito, F ;
Girelli, D ;
Totaro, A ;
Carella, M ;
Grifa, A ;
Gasparini, P .
EUROPEAN JOURNAL OF HUMAN GENETICS, 1997, 5 (06) :371-375
[3]   C/EBPα regulates hepatic transcription of hepcidin, an antimicrobial peptide and regulator of iron metabolism [J].
Courselaud, B ;
Pigeon, C ;
Inoue, Y ;
Inoue, J ;
Gonzalez, FJ ;
Leroyer, P ;
Gilot, D ;
Boudjema, K ;
Guguen-Guillouzo, C ;
Brissott, P ;
Loréal, O ;
Ilyin, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (43) :41163-41170
[4]   Hepcidin expression inversely correlates with the expression of duodenal iron transporters and iron absorption in rats [J].
Frazer, DM ;
Wilkins, SJ ;
Becker, EM ;
Vulpe, CD ;
McKie, AT ;
Trinder, D ;
Anderson, GJ .
GASTROENTEROLOGY, 2002, 123 (03) :835-844
[5]   The orchestration of body iron intake: how and where do enterocytes receive their cues? [J].
Frazer, DM ;
Anderson, GJ .
BLOOD CELLS MOLECULES AND DISEASES, 2003, 30 (03) :288-297
[6]   Delayed hepcidin response explains the lag period in iron absorption following a stimulus to increase erythropoiesis [J].
Frazer, DM ;
Inglis, HR ;
Wilkins, SJ ;
Millard, KN ;
Steele, TM ;
McLaren, GD ;
McKie, AT ;
Vulpe, CD ;
Anderson, GJ .
GUT, 2004, 53 (10) :1509-1515
[7]   Increased hepcidin expression and hypoferraemia associated with an acute phase response are not affected by inactivation of HFE [J].
Frazer, DM ;
Wilkins, SJ ;
Millard, KN ;
McKie, AT ;
Vulpe, CD ;
Anderson, GJ .
BRITISH JOURNAL OF HAEMATOLOGY, 2004, 126 (03) :434-436
[8]   Is TfR2 the iron sensor? [J].
Ganz, T .
BLOOD, 2004, 104 (13) :3839-3840
[9]   Balancing acts: Molecular control of mammalian iron metabolism [J].
Hentze, MW ;
Muckenthaler, MU ;
Andrews, NC .
CELL, 2004, 117 (03) :285-297
[10]   The solution structure of human hepcidin, a peptide hormone with antimicrobial activity that is involved in iron uptake and hereditary hemochromatosis [J].
Hunter, HN ;
Fulton, DB ;
Ganz, T ;
Vogel, HJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (40) :37597-37603