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Am J Physiol Renal Physiol (July 22, 2003). doi:10.1152/ajprenal.00064.2003
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Submitted on February 14, 2003
Accepted on July 17, 2003

Altered dietary iron intake is a strong modulator of renal DMT1 expression

Mark Wareing1, Carole J. Ferguson1, Mathieu Delannoy1, Alan G. Cox2, Raymond F.T. McMahon3, Roger Green1, Daniela Riccardi1, and Craig P. Smith1*

1 School of Biological Sciences, University of Manchester, Manchester, Greater Manchester, United Kingdom
2 Centre for Analytical Sciences, University of Sheffield, Sheffield, Yorkshire, United Kingdom
3 Laboratory Medicine Academic Group, Faculty of Medicine, University of Manchester and Department of Histopathology, Manchester Royal Infirmary, Manchester, Greater Manchester, United Kingdom

* To whom correspondence should be addressed. E-mail: Craig.Smith{at}man.ac.uk.

Divalent metal transporter1 (DMT1, also known as DCT1 or NRAMP2) is an important component of the cellular machinery responsible for dietary iron absorption in the duodenum. DMT1 is also highly expressed in the kidney where it has been suggested to play a role in urinary iron handling. In this study we determined the effect on renal DMT1 expression of feeding an iron-restricted diet (50mg/kg) or an iron-enriched diet (5g/kg) for four weeks and measured urinary and fecal iron excretion rates. Feeding the low iron diet caused a reduction in serum iron concentration, fecal iron output rate and an increase in renal DMT1 expression. Feeding an iron-enriched diet had the converse effect. Therefore, DMT1 expression in the kidney is sensitive to dietary iron intake, and the level of expression is inversely related to the dietary iron content. Changes in DMT1 expression occurred intracellularly in the proximal tubule and in the apical membrane and sub apical region of the distal convoluted tubule. Increased DMT1 expression was accompanied by a decrease in urinary iron excretion rate, and vice versa when DMT1 expression was reduced. Together these findings suggest that modulation of renal DMT1 expression may influence renal iron excretion rate.




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