Recent advances in mammalian haem transport

被引:84
作者
Latunde-Dada, GO
Simpson, RJ
McKie, AT
机构
[1] Kings Coll London, Dept Biochem, London SE1 9NH, England
[2] Kings Coll London, Div Nutr Sci, London SE1 9NH, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1016/j.tibs.2006.01.005
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
Haem is a structural component of numerous cellular proteins and contributes greatly to iron metabolic processes in mammals. Haem-carrier protein 1 (HCP1) has recently been cloned and characterized as a putative transporter in the apical region of the duodenum, and is responsible for uptake of haem into the gut cells. Its expression is regulated pre- and post-translationally in hypoxic and iron-deficient mice, respectively. The identification of HCP1 has revealed the long-sought mechanism by which haem - an important source of dietary iron - is absorbed from the diet by the gut. Feline leukaemic virus receptor (FLCVR) and ABC transporter ABCG2, characterized in haematopoietic cells, have also recently been shown to export haem, particularly under stress. FLVCR protects developing erythroid cells from haem toxicity during the early stages of differentiation, and ABCG2 averts protoporphyrin accumulation (particularly under hypoxic conditions). These haem-efflux proteins are expressed in other cells and tissues including the intestine where they might function as apical haem exporters to prevent toxicity in the enterocytes.
引用
收藏
页码:182 / 188
页数:7
相关论文
共 70 条
[1]   A novel mammalian iron-regulated protein involved in intracellular iron metabolism [J].
Abboud, S ;
Haile, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (26) :19906-19912
[2]   RETROVIRUS-INDUCED FELINE PURE RED-CELL APLASIA - HEMATOPOIETIC PROGENITORS ARE INFECTED WITH FELINE LEUKEMIA-VIRUS AND ERYTHROID BURST-FORMING CELLS ARE UNIQUELY SENSITIVE TO HETEROLOGOUS COMPLEMENT [J].
ABKOWITZ, JL ;
HOLLY, RD ;
GRANT, CK .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 80 (04) :1056-1063
[3]   Hepatic iron metabolism [J].
Anderson, GJ ;
Frazer, DM .
SEMINARS IN LIVER DISEASE, 2005, 25 (04) :420-432
[4]   PORPHYRIN ACCUMULATION IN THE HARDERIAN GLANDS OF FEMALE SYRIAN-HAMSTER RESULTS IN MITOCHONDRIAL DAMAGE AND CELL-DEATH [J].
ANTOLIN, I ;
URIA, H ;
TOLIVIA, D ;
RODRIGUEZCOLUNGA, MJ ;
RODRIGUEZ, C ;
KOTLER, ML ;
MENENDEZPELAEZ, A .
ANATOMICAL RECORD, 1994, 239 (04) :349-359
[5]   Promoter characterization and genomic organization of the human breast cancer resistance protein (ATP-binding cassette transporter G2) gene [J].
Bailey-Dell, KJ ;
Hassel, B ;
Doyle, LA ;
Ross, DD .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2001, 1520 (03) :234-241
[6]  
BANNERMAN RM, 1965, NEW YORK STATE J MED, V65, P1634
[7]   TIN-MESOPORPHYRIN INHIBITS HEME OXYGENASE ACTIVITY AND HEME-IRON ABSORPTION IN THE INTESTINE [J].
BONI, RE ;
BONI, RAH ;
GALBRAITH, RA ;
DRUMMOND, GS ;
KAPPAS, A .
PHARMACOLOGY, 1993, 47 (05) :318-329
[8]   In vitro formation of a c-type cytochrome [J].
Daltrop, O ;
Allen, JWA ;
Willis, AC ;
Ferguson, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (12) :7872-7876
[9]   The human ATP-binding cassette (ABC) transporter superfamily [J].
Dean, M ;
Rzhetsky, A ;
Allikmets, R .
GENOME RESEARCH, 2001, 11 (07) :1156-1166
[10]   A physiological model to study iron recycling in macrophages [J].
Delaby, C ;
Pilard, N ;
Hetet, G ;
Driss, F ;
Grandchamp, B ;
Beaumont, C ;
Canonne-Hergaux, F .
EXPERIMENTAL CELL RESEARCH, 2005, 310 (01) :43-53