Iron metabolism in mammalian cells

被引:22
作者
Walker, BL
Tiong, JWC
Jefferies, WA
机构
[1] Univ British Columbia, Biotechnol Lab, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Biomed Res Ctr, Vancouver, BC V6T 1Z3, Canada
[3] Univ British Columbia, Dept Med Genet Microbiol & Immunol, Vancouver, BC V6T 1Z3, Canada
[4] Univ British Columbia, Dept Zool, Vancouver, BC V6T 1Z3, Canada
来源
INTERNATIONAL REVIEW OF CYTOLOGY - A SURVEY OF CELL BIOLOGY, VOL 211 | 2001年 / 211卷
关键词
iron metabolism; iron absorption; DMT-1; IREG; transferrin; transferrin receptor; melanotransferrin; ferritin;
D O I
10.1016/S0074-7696(01)11020-X
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Most living things require iron to exist. Iron has many functions within cells but is rarely found unbound because of its propensity to catalyze the formation of toxic free radicals. Thus the regulation of iron requirements by cells and the acquisition and uptake of iron into tissues in multicellular organisms is tightly regulated. In humans, understanding iron transport and utility has recently been advanced by a "great conjunction" of molecular genetics in simple organisms, identifying genes involved in genetic diseases of metal metabolism and by the application of traditional cell physiology approaches. We are now able to approach a rudimentary understanding of the "iron cycle" within mammals. In the future, this information will be applied toward modulating the outcome of therapies designed to overcome diseases involving metals. © 2001 Academic Press.
引用
收藏
页码:241 / 278
页数:38
相关论文
共 244 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]   Genotypic/phenotypic correlations in genetic hemochromatosis: Evolution of diagnostic criteria [J].
Adams, PC ;
Chakrabarti, S .
GASTROENTEROLOGY, 1998, 114 (02) :319-323
[3]  
ALEMANY R, 1993, J CELL SCI, V104, P1155
[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]  
Alvarez-Hernandez X, 1998, BLOOD, V91, P3974
[6]   Apo-transferrin is internalized and routed differently from Fe-transferrin by Caco-2 cells: a confocal microscopy study of vesicular transport in intestinal cells [J].
Alvarez-Hernandez, X ;
Smith, M ;
Glass, J .
BLOOD, 2000, 95 (02) :721-723
[7]   APOLACTOFERRIN STRUCTURE DEMONSTRATES LIGAND-INDUCED CONFORMATIONAL CHANGE IN TRANSFERRINS [J].
ANDERSON, BF ;
BAKER, HM ;
NORRIS, GE ;
RUMBALL, SV ;
BAKER, EN .
NATURE, 1990, 344 (6268) :784-787
[8]   Medical progress: Disorders of iron metabolism [J].
Andrews, NC .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (26) :1986-1995
[9]  
Andrews NC, 2000, NEW ENGL J MED, V342, P364
[10]   THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :129-157