4.7 Article

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

Journal

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
Volume 284, Issue 1, Pages C44-C50

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpcell.00184.2002

Keywords

divalent metal transporter 1; transport; intestine

Funding

  1. NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES [R01ES008755, P01ES008131, P30ES003819] Funding Source: NIH RePORTER
  2. NIEHS NIH HHS [R01 ES 08755, P01 ES 08131, ES 03819] Funding Source: Medline

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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.

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