Non-transferrin bound iron: A key role in iron overload and iron toxicity

被引:479
作者
Brissot, Pierre [1 ,2 ,3 ,4 ]
Ropert, Martine [1 ,4 ,5 ]
Le Lan, Caroline [1 ,3 ,4 ]
Loreal, Olivier [1 ,2 ,3 ,4 ]
机构
[1] INSERM, UMR991, F-35033 Rennes, France
[2] Univ Rennes 1, F-35043 Rennes, France
[3] CHU Rennes, Liver Dis Dept, F-35033 Rennes, France
[4] CHU Rennes, Natl Reference Ctr Rare Genet Iron Overload Disor, F-35033 Rennes, France
[5] CHU Rennes, Dept Biochem, F-35033 Rennes, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2012年 / 1820卷 / 03期
关键词
Non-transferrin bound iron (NTBI); Hepcidin; Ferroportin; Iron overload; Hemochromatosis; Thalassemia; LABILE PLASMA IRON; HEREDITARY HEMOCHROMATOSIS PROTEIN; RECEIVING INTRAVENOUS IRON; BLEOMYCIN-DETECTABLE IRON; ISOLATED RAT HEPATOCYTES; SICKLE-CELL-DISEASE; HFE KNOCKOUT MOUSE; CHELATION-THERAPY; DIETARY IRON; HEMODIALYSIS-PATIENTS;
D O I
10.1016/j.bbagen.2011.07.014
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
Background: Besides transferrin iron, which represents the normal form of circulating iron, non-transferrin bound iron (NTBI) has been identified in the plasma of patients with various pathological conditions in which transferrin saturation is significantly elevated. Scope of the review: To show that: i) NTBI is present not only during chronic iron overload disorders (hemochromatosis, transfusional iron overload) but also in miscellaneous diseases which are not primarily iron overloaded conditions; ii) this iron species represents a potentially toxic iron form due to its high propensity to induce reactive oxygen species and is responsible for cellular damage not only at the plasma membrane level but also towards different intracellular organelles; iii) the NTBI concept may be expanded to include intracytosolic iron forms which are not linked to ferritin, the major storage protein which exerts, at the cellular level, the same type of protective effect towards the intracellular environment as transferrin in the plasma. Major conclusions: Plasma NTBI and especially labile plasma iron determinations represent a new important biological tool since elimination of this toxic iron species is a major therapeutic goal. General significance: The NTBI approach represents an important mechanistic concept for explaining cellular iron excess and toxicity and provides new important biochemical diagnostic tools. This article is part of a Special Issue entitled Transferrins: Molecular mechanisms of iron transport and disorders. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:403 / 410
页数:8
相关论文
共 127 条
[41]  
Garrick LM, 1999, J CELL PHYSIOL, V178, P349, DOI 10.1002/(SICI)1097-4652(199903)178:3<349::AID-JCP9>3.0.CO
[42]  
2-R
[43]   No evidence for myocardial iron overload and free iron species in multitransfused patients with sickle/β0-thalassaemia [J].
Ghoti, Hussam ;
Goitein, Orly ;
Koren, Ariel ;
Levin, Carina ;
Kushnir, Tamar ;
Rachmilewitz, Eliezer ;
Konen, Eli .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2010, 84 (01) :59-63
[44]   Quantification of non-transferrin-bound iron in the presence of unsaturated transferrin [J].
Gosriwatana, I ;
Loreal, O ;
Lu, S ;
Brissot, P ;
Porter, J ;
Hider, RC .
ANALYTICAL BIOCHEMISTRY, 1999, 273 (02) :212-220
[45]   Characterisation of citrate and iron citrate uptake by cultured rat hepatocytes [J].
Graham, RM ;
Morgan, EH ;
Baker, E .
JOURNAL OF HEPATOLOGY, 1998, 29 (04) :603-613
[46]   Transferrin receptor 2 mediates uptake of transferrin-bound and non-transferrin-bound iron [J].
Graham, Ross M. ;
Reutens, Gail M. ;
Herbison, Carly E. ;
Delima, Roheeth D. ;
Chua, Anita C. G. ;
Olynyk, John K. ;
Trinder, Debbie .
JOURNAL OF HEPATOLOGY, 2008, 48 (02) :327-334
[47]  
GROOTVELD M, 1989, J BIOL CHEM, V264, P4417
[48]   Cybrd1 (duodenal cytochrome b) is not necessary for dietary iron absorption in mice [J].
Gunshin, H ;
Starr, CN ;
DiRenzo, C ;
Fleming, MD ;
Jin, J ;
Greer, EL ;
Sellers, VM ;
Galica, SM ;
Andrews, NC .
BLOOD, 2005, 106 (08) :2879-2883
[49]   Slc11a2 is required for intestinal iron absorption and erythropoiesis but dispensable in placenta and liver [J].
Gunshin, H ;
Fujiwara, Y ;
Custodio, AO ;
DiRenzo, C ;
Robine, S ;
Andrews, NC .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (05) :1258-1266
[50]   Cloning and characterization of a mammalian proton-coupled metal-ion transporter [J].
Gunshin, H ;
Mackenzie, B ;
Berger, UV ;
Gunshin, Y ;
Romero, MF ;
Boron, WF ;
Nussberger, S ;
Gollan, JL ;
Hediger, MA .
NATURE, 1997, 388 (6641) :482-488