Iron and copper interactions in development and the effect on pregnancy outcome

Journal of Nutrition

Volumn 133, Issue 5 SUPPL. 2, 2003, Pages

  Gambling, Lorraine ^a   Danzeisen, Ruth ^a   Fosset, Cedric ^a   Andersen, Henriette S ^a   Dunford, Susan ^a   Srai, S Kaila S ^b   McArdle, Harry J ^a  

^a ROWETT RESEARCH INSTITUTE   (United Kingdom)

^b ROYAL FREE HOSPITAL   (United Kingdom)

Author keywords

BeWo cells; Deficiency; Human; Micronutrients; Placental transfer; Rat

Indexed keywords

CERULOPLASMIN; COPPER; IRON; NATURAL RESISTANCE ASSOCIATED MACROPHAGE PROTEIN 2; OXIDOREDUCTASE; TRACE ELEMENT; TRANSFERRIN RECEPTOR; TUMOR NECROSIS FACTOR ALPHA; TUMOR NECROSIS FACTOR RECEPTOR 1;

CONFERENCE PAPER; COPPER DEFICIENCY; FETUS DEVELOPMENT; GENE; HUMAN; HUMAN CELL; INTRAUTERINE GROWTH RETARDATION; IRON DEFICIENCY; IRON OVERLOAD; IRON REGULATED GENE 1; IRON RESPONSIVE ELEMENT; NONHUMAN; PLACENTAL TRANSFER; PREGNANCY;

EID: 0038670714     PISSN: 00223166     EISSN: None     Source Type: Journal    
DOI: 10.1093/jn/133.5.1554s     Document Type: Conference Paper

References (20)

1. Schwartz, W. J., 3rd & Thurnau, G. R. (1995) Iron deficiency anemia in pregnancy. Clin. Obstet. Gynecol. 38: 443-454.
2. Bothwell, T. H. (2000) Iron requirements in pregnancy and strategies to meet them. Am. J. Clin. Nutr. 72: 257S-264S.
3. Allen, L. H. (2000) Anemia and iron deficiency: effects on pregnancy outcome. Am. J. Clin. Nutr. 71: 1280S-1284S.
4. Godfrey, K. M., Redman, C. W., Barker, D. J. & Osmond, C. (1991) The effect of maternal anaemia and iron deficiency on the ratio of fetal weight to placental weight Br. J. Obstet. Gynaecol. 98: 886-891.
5. Kwik-Udbe, C. L., Gietzen, D., German, J. B., Golub, M. S. & Keen, C. L. (2000) Chronic marginal iron intakes during early development in mice result in persistent changes in dopamine metabolism and myelin composition. J. Nutr. 130: 2821-2830.
6. Tuttle, S., Aggett, P. J., Campbell, D. & MacGillivray, I. (1985) Zinc and copper nutrition in human pregnancy: a longitudinal study in normal primigravidae and in primigravidae at risk of delivering a growth retarded baby. Am. J. Clin. Nutr. 41: 1032-1041.
7. Linder, M. (1991) The Biochemistry of Copper. Plenum Press, New York.
8. Krachler, M., Rossipal, E. & Micetic-Turk, D. (1999) Trace element transfer from the mother to the newborn-investigations on triplets of colostrum, maternal and umbilical cord sera. Eur. J. Clin. Nutr. 53: 486-494.
9. Keen, C. L., Uriu-Hare, J. Y., Hawk, S. N., Jankowski, M. A., Daston, G. P., Kwik-Uribe, C. L. & Rucker, R. B. (1998) Effect of copper deficiency on prenatal development and pregnancy outcome. Am. J. Clin. Nutr. 67: 1003S-1011S.
10. Wapnir, R. A., Gyasi, I., Harper, R. G., Moyse, J. & Teichberg, S. (1996) Placental copper transport in the rat. II: Effect of maternal copper deficiency. Placenta 17: 479-486.
11. Tong, K. K. & McArdle, H. J. (1995) Copper uptake by cultured trophoblast cells isolated from human term placenta. Biochim. Biophys. Acta 1269: 233-236.
12. McArdle, H. J. & van den Berg, G. J. (1992) The accumulation of copper by microvillar vesicles isolated from human placenta. J. Nutr. 122: 1260-1265.
13. Lee, S. H., Lancey, R., Montaser, A., Madani, N. & Linder, M. C., (1993) Ceruloplasmin and copper transport during the latter part of gestation in the rat. Proc. Soc. Exp. Biol. Med. 203: 428-439.
14. Hilton, M., Spenser, D. C., Ross, P., Ramsey, A. & McArdle, H. J. (1995) Characterisation of the copper uptake mechanism and isolation of the ceruloplasmin receptor/copper transporter in human placental vesicles. Biochim. Biophys. Acta 1245: 153-160.
15. Harris, Z. L., Durley, A. P., Man, T. K. & Gitlin, J. D. (1999) Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux. Proc. Natl. Acad. Sci. USA 96: 10812-10817.
16. Zhou, B. & Gitschier, J. (1997) hCTR1: a human gene for copper uptake identified by complementation in yeast. Proc. Natl. Acad. Sci. USA 94: 7481-7486.
17. Kuo, Y. M., Zhou, B., Cosco, D. & Gitschier, J. (2001) The copper transporter CTR1 provides an essential function in mammalian embryonic development. Proc. Natl. Acad. Sci. USA 98: 6836-6841.
18. Lee, J., Prohaska, J. R. & Thiele, D. J. (2001) Essential role for mammalian copper transporter Ctrl in copper homeostasis and embryonic development. Proc. Natl. Acad. Sci. USA 98: 6842-6847.
19. Kuo, Y. M., Gitschier, J. & Packman, S. (1999) Developmental expression of the mouse mottled and toxic milk genes. Adv. Exp. Med. Biol. 448: 109-114.
20. Buiakova, O. I., Xu, J., Lutsenko, S., Zeitlin, S., Das, K., Das, S., Ross, B. M., Mekios, C., Scheinberg, H. & Gilliam, T. C. (1999) Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation. Hum. Mol. Genet. 8: 1665-1671.