Divalent metal transporter 1 in lead and cadmium transport

被引:195
作者
Bressler, JP
Olivi, L
Cheong, JH
Kim, Y
Bannon, D
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 USA
[3] Sahmyook Univ, Sch Pharm, Seoul, South Korea
[4] Soonchunhyang Univ, Dept Prevent Med, Chunan, South Korea
来源
REDOX-ACTIVE METALS IN NEUROLOGICAL DISORDERS | 2004年 / 1012卷
关键词
divalent metal transporter 1 (DMT1); transport; cadmium (Cd); lead (Pb); diet;
D O I
10.1196/annals.1306.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The effect of exposure to cadmium (Cd) and lead (Pb) on human health has been recognized for many years and recent information suggests that minimal exposure levels are themselves too high. Common scenarios for Ph exposure include occupational, residential, and/or behavioral (hand-to-mouth activity) settings. The main source of Cd exposure for nonsmokers is dietary, through plants or animals that accumulate the metal. Specific cellular importers for Ph and Cd are unlikely as these metals are nonessential and toxic. Accordingly, in the intestine, the operational mechanism is assumed to be inadvertent uptake through pathways intended for essential nutrients such as iron. Results from experimental and epidemiological Studies indicated that diets low in iron (Fe) result in increased absorption of Pb and Cd, suggesting common molecular mechanisms of Cd and Ph transport. Indeed, recent mechanistic studies found that the intestinal transporter for nonheme iron, divalent metal transporter 1 (DMT1), mediates the transport of Pb and Cd. DMT1 is regulated, in part, by dietary iron, and chemical species of Cd and Ph that are transported by DMTI would be made available through digestion and are also found in plasma. Accordingly, the involvement of DMT1 in metal uptake offers a mechanistic explanation for why an iron-deficient diet is a risk factor for Ph and Cd poisoning. It also suggests that diets rich in iron-containing food could be protective against heavy metal poisoning.
引用
收藏
页码:142 / 152
页数:11
相关论文
共 87 条
  • [1] A novel mammalian iron-regulated protein involved in intracellular iron metabolism
    Abboud, S
    Haile, DJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (26) : 19906 - 19912
  • [2] Chemistry and biology of eukaryotic iron metabolism
    Aisen, P
    Enns, C
    Wessling-Resnick, M
    [J]. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2001, 33 (10) : 940 - 959
  • [3] Cadmium exposure in pregnancy and lactation in relation to iron status
    Åkesson, A
    Berglund, M
    Schütz, A
    Bjellerup, P
    Bremme, K
    Vahter, M
    [J]. AMERICAN JOURNAL OF PUBLIC HEALTH, 2002, 92 (02) : 284 - 287
  • [4] EXPERIMENTAL LOCALIZATION OF INTESTINAL UPTAKE SITES FOR METALS (CD, HG, ZN, SE) IN-VIVO IN MICE
    ANDERSEN, O
    NIELSEN, JB
    SORENSEN, JA
    SCHERREBECK, L
    [J]. ENVIRONMENTAL HEALTH PERSPECTIVES, 1994, 102 : 199 - 206
  • [5] The ceruloplasmin homolog hephaestin and the control of intestinal iron absorption
    Anderson, GJ
    Frazer, DM
    McKie, AT
    Vulpe, CD
    [J]. BLOOD CELLS MOLECULES AND DISEASES, 2002, 29 (03) : 367 - 375
  • [6] DMT1, a physiologically relevant apical Cu1+ transporter of intestinal cells
    Arredondo, M
    Muñoz, P
    Mura, CV
    Núñez, MT
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2003, 284 (06): : C1525 - C1530
  • [7] KINETIC CHARACTERIZATION OF INVITRO LEAD TRANSPORT ACROSS THE RAT SMALL-INTESTINE - MECHANISM OF INTESTINAL LEAD TRANSPORT
    AUNGST, BJ
    FUNG, HL
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 1981, 61 (01) : 39 - 47
  • [8] Effect of DMT1 knockdown on iron, cadmium, and lead uptake in Caco-2 cells
    Bannon, DI
    Abounader, R
    Lees, PSJ
    Bressler, JP
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2003, 284 (01): : C44 - C50
  • [9] Uptake of lead and iron by divalent metal transporter 1 in yeast and mammalian cells
    Bannon, DI
    Portnoy, ME
    Olivi, L
    Lees, PSJ
    Culotta, VC
    Bressler, JP
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 295 (04) : 978 - 984
  • [10] ACTIVE-TRANSPORT OF PB-210 BY EVERTED SEGMENTS OF RAT DUODENUM
    BARTON, JC
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1984, 247 (02): : G193 - G198