Effect of DMT1 knockdown on iron, cadmium, and lead uptake in Caco-2 cells

被引:171
作者
Bannon, DI
Abounader, R
Lees, PSJ
Bressler, JP
机构
[1] Kennedy Krieger Inst, Dept Neurol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Environm Hlth Sci, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2003年 / 284卷 / 01期
关键词
divalent metal transporter 1; transport; intestine;
D O I
10.1152/ajpcell.00184.2002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
DMT1 (divalent metal transporter 1) is a hydrogen-coupled divalent metal transporter with a substrate preference for iron, although the protein when expressed in frog oocytes transports a broad range of metals, including the toxic metals cadmium and lead. Wild-type Caco-2 cells displayed saturable transport of lead and iron that was stimulated by acid. Cadmium and manganese inhibited transport of iron, but zinc and lead did not. The involvement of DMT1 in the transport of toxic metals was examined by establishing clonal DMT1 knockdown and control Caco-2 cell lines. Knockdown cell lines displayed much lower levels of DMT1 mRNA and a smaller V-max for iron uptake compared with control cell lines. One clone was further characterized and found to display an similar to50% reduction in uptake of iron across a pH range from 5.5 to 7.4. Uptake for cadmium also decreased 50% across the same pH range, but uptake for lead did not. These results show that DMT1 is important in iron and cadmium transport in Caco-2 cells but that lead enters these cells through an independent hydrogen-driven mechanism.
引用
收藏
页码:C44 / C50
页数:7
相关论文
共 33 条
[1]   Reversion of human glioblastoma malignancy by U1 small nuclear RNA/ribozyme targeting of scatter factor/hepatocyte growth factor and c-met expression [J].
Abounader, R ;
Ranganathan, S ;
Lal, B ;
Fielding, K ;
Book, A ;
Dietz, H ;
Burger, P ;
Laterra, J .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (18) :1548-1556
[2]   Chemistry and biology of eukaryotic iron metabolism [J].
Aisen, P ;
Enns, C ;
Wessling-Resnick, M .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2001, 33 (10) :940-959
[3]   Phlebotomy increases cadmium uptake in hemochromatosis [J].
Åkesson, A ;
Stål, P ;
Vahter, M .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2000, 108 (04) :289-291
[4]  
BANNON DI, 1994, CLIN CHEM, V40, P1730
[5]   Uptake of lead and iron by divalent metal transporter 1 in yeast and mammalian cells [J].
Bannon, DI ;
Portnoy, ME ;
Olivi, L ;
Lees, PSJ ;
Culotta, VC ;
Bressler, JP .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 295 (04) :978-984
[6]  
BARTON JC, 1994, J LAB CLIN MED, V124, P193
[7]   Iron deficiency associated with higher blood lead in children living in contaminated environments [J].
Bradman, A ;
Eskenazi, B ;
Sutton, P ;
Athanasoulis, M ;
Goldman, LR .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2001, 109 (10) :1079-1084
[8]   Cellular and subcellular localization of the Nramp2 iron transporter in the intestinal brush border and regulation by dietary iron [J].
Canonne-Hergaux, F ;
Gruenheid, S ;
Ponka, P ;
Gros, P .
BLOOD, 1999, 93 (12) :4406-4417
[9]  
CHANTRET I, 1987, CANCER RES, V47, P1426
[10]   Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter [J].
Donovan, A ;
Brownlie, A ;
Zhou, Y ;
Shepard, J ;
Pratt, SJ ;
Moynihan, J ;
Paw, BH ;
Drejer, A ;
Barut, B ;
Zapata, A ;
Law, TC ;
Brugnara, C ;
Kingsley, PD ;
Palis, J ;
Fleming, MD ;
Andrews, NC ;
Zon, LI .
NATURE, 2000, 403 (6771) :776-781