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Am J Physiol Gastrointest Liver Physiol 296: G798-G804, 2009. First published January 29, 2009; doi:10.1152/ajpgi.90342.2008
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LIVER AND BILIARY TRACT

Small molecule inhibitors of divalent metal transporter-1

Peter D. Buckett and Marianne Wessling-Resnick

Harvard School of Public Health, Department of Genetics and Complex Diseases, Boston, Massachusetts

Submitted 19 May 2008 ; accepted in final form 28 January 2009

Divalent metal transporter-1 (DMT1) is a divalent cation transporter that plays a key role in iron metabolism by mediating ferrous iron uptake across the small intestine. We have previously identified several small molecule inhibitors of iron uptake (4). Using a cell line that stably overexpresses DMT1, we screened the ability of these inhibitors to specifically block this transporter's activity. One compound, NSC306711, inhibited DMT1-mediated iron uptake in a reversible and competitive manner. This inhibitor is a polysulfonated dye containing two copper centers. Although one of these two sites could be chelated by Triethylenetetramine copper chelation did not perturb NSC306711 inhibition of DMT1 activity. Several other polysulfonated dyes with structural features similar to NSC306711 were identified as potential DMT1 transport inhibitors. This study characterizes important pharmacological tools that can be used to probe DMT1's mechanism of iron transport and its role in iron metabolism.

iron; iron transport inhibitors



Address for reprint requests and other correspondence: M. Wessling-Resnick, Harvard School of Public Health, Dept. of Genetics and Complex Diseases, 665 Huntington Ave., Boston, MA 02115 (e-mail: wessling{at}hsph.harvard.edu)







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