Iron overload and immunity

被引:0
作者
Graca Porto
Maria De Sousa
机构
[1] IBMC
[2] ICBAS Abel Salazar Institute for the Biomedical Sciences
[3] Institute of Molecular and Cellular Biology
[4] Porto
[5] Porto 823 4150
[6] Portugal HGSA
[7] Santo António General Hospital
关键词
Iron; Iron overload; Innate immunity; Adaptive immunity;
D O I
暂无
中图分类号
R55 [血液及淋巴系疾病];
学科分类号
1002 ; 100201 ;
摘要
Progress in the characterization of genes involved in the control of iron homeostasis in humans and in mice has improved the definition of iron overload and of the cells affected by it.The cell involved in iron overload with the greatest effect on immunity is the macrophage. Intriguing evidence has emerged,however,in the last 12 years indicating that parenchymal iron overload is linked to genes classically associated with the immune system.This review offers an update of the genes and proteins relevant to iron metabolism expressed in cells of the innate immune system,and addresses the question of how this system is affected in clinical situations of iron overload.The relationship between iron and the major cells of adaptive immunity,the T lymphocytes, will also be reviewed.Most studies addressing this last question in humans were performed in the clinical model of Hereditary Hemochromatosis.Data will also be reviewed demonstrating how the disruption of molecules essentially involved in adaptive immune responses result in the spontaneous development of iron overload and how they act as modifiers of iron overload.
引用
收藏
页码:4707 / 4715
页数:9
相关论文
共 20 条
[1]  
Expression of iron transport proteins divalent metal transporter‐1, Ferroportin‐1, HFE and transferrin receptor‐1 in human monocyte‐derived dendritic cells[J] . MartinBrinkmann,ReginaTeuffel,NihayLaham,RachelEhrlich,PatriceDecker,Francois A.Lemonnier,StevePascolo.Cell Biochem. Funct. . 2007 (3)
[2]   Prohepcidin localises to the Golgi compartment and secretory pathway in hepatocytes [J].
Wallace, DF ;
Summerville, L ;
Lusby, PE ;
Subramaniam, VN .
JOURNAL OF HEPATOLOGY, 2005, 43 (04) :720-728
[3]  
Hepcidin: A direct link between iron metabolism and immunity[J] . International Journal of Biochemistry and Cell Biology . 2005 (9)
[4]   Transferrin is required for early T-cell differentiation [J].
Macedo, MF ;
de Sousa, M ;
Ned, RM ;
Mascarenhas, C ;
Andrews, NC ;
Correia-Neves, M .
IMMUNOLOGY, 2004, 112 (04) :543-549
[5]   Molecular analysis of iron overload in β2-microglobulin-deficient mice [J].
Muckenthaler, MU ;
Rodrigues, P ;
Macedo, MG ;
Minana, B ;
Brennan, K ;
Cardoso, EM ;
Hentze, MW ;
de Sousa, M .
BLOOD CELLS MOLECULES AND DISEASES, 2004, 33 (02) :125-131
[6]  
TOLL-LIKE RECEPTORS[J] . Kiyoshi Takeda,Tsuneyasu Kaisho,Shizuo Akira.Annual Review of Immunology . 2003
[7]   The neutrophil lipocalin NGAL is a bacteriostatic agent that interferes with siderophore-mediated iron acquisition [J].
Goetz, DH ;
Holmes, MA ;
Borregaard, N ;
Bluhm, ME ;
Raymond, KN ;
Strong, RK .
MOLECULAR CELL, 2002, 10 (05) :1033-1043
[8]   Decreased liver hepcidin expression in the Hfe knockout mouse [J].
Ahmad, KA ;
Ahmann, JR ;
Migas, MC ;
Waheed, A ;
Britton, RS ;
Bacon, BR ;
Sly, WS ;
Fleming, RE .
BLOOD CELLS MOLECULES AND DISEASES, 2002, 29 (03) :361-366
[9]   Peripheral lymphocytes and intracellular cytokines in C282Y homozygous hemochromatosis patients [J].
Fabio, G ;
Zarantonello, M ;
Mocellin, C ;
Bonara, P ;
Corengia, C ;
Fargion, S ;
Fiorelli, G .
JOURNAL OF HEPATOLOGY, 2002, 37 (06) :753-761
[10]   Antiviral activities of lactoferrin [J].
van der Strate, BWA ;
Beljaars, L ;
Molema, G ;
Harmsen, MC ;
Meijer, DKF .
ANTIVIRAL RESEARCH, 2001, 52 (03) :225-239