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J. Nutr. First published February 11, 2009; doi:10.3945/jn.108.096354
Journal of Nutrition, doi:10.3945/jn.108.096354
Vol. 139, No. 4, 672-679, April 2009

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© 2009 American Society for Nutrition


Ingestive Behavior and Neurosciences

Iron Is Essential for Neuron Development and Memory Function in Mouse Hippocampus1–3,

Erik S. Carlson4–7, Ivan Tkac8, Rhamy Magid6, Michael B. O'Connor9,10, Nancy C. Andrews11, Timothy Schallert10,11, Hiromi Gunshin14,15, Michael K. Georgieff5–7* and Anna Petryk6,9

4 Medical Scientist Training Program, 5 Graduate Program in Neuroscience, 6 Pediatrics, 7 Center for Neurobehavioral Development, 8 Center for Magnetic Resonance Research, and 9 Genetics, Cell Biology and Development, University of Minnesota Medical School, Minneapolis, MN 55455; 10 Howard Hughes Medical Institute, Chevy Chase, MD 20815; 11 Duke University School of Medicine, Durham, NC 27710; 12 Institute for Neuroscience, and 13 Department of Psychology, University of Texas, Austin, TX 78712; and 14 Department of Nutrition, University of Massachusetts, Amherst, MA 01003

Iron deficiency (ID) is the most prevalent micronutrient deficiency in the world and it affects neurobehavioral outcome. It is unclear whether the effect of dietary ID on the brain is due to the lack of neuronal iron or from other processes occurring in conjunction with ID (e.g. hypoxia due to anemia). We delineated the role of murine Slc11a2 [divalent metal ion transporter-1 (DMT-1)] in hippocampal neuronal iron uptake during development and memory formation. Camk2a gene promoter-driven cre recombinase (Cre) transgene (Camk2a-Cre) mice were mated with Slc11a2 flox/flox mice to obtain nonanemic Slc11a2hipp/hipp (double mutant, hippocampal neuron-specific knockout of Slc11a2hipp/hipp) mice, the first conditionally targeted model of iron uptake in the brain. Slc11a2hipp/hipp mice had lower hippocampal iron content; altered developmental expression of genes involved in iron homeostasis, energy metabolism, and dendrite morphogenesis; reductions in markers for energy metabolism and glutamatergic neurotransmission on magnetic resonance spectroscopy; and altered pyramidal neuron dendrite morphology in area 1 of Ammon's Horn in the hippocampus. Slc11a2hipp/hipp mice did not reach the criterion on a difficult spatial navigation test but were able to learn a spatial navigation task on an easier version of the Morris water maze (MWM). Learning of the visual cued task did not differ between the Slc11a2WT/WT and Slc11a2hipp/hipp mice. Slc11a2WT/WT mice had upregulation of genes involved in iron uptake and metabolism in response to MWM training, and Slc11a2hipp/hipp mice had differential expression of these genes compared with Slc11a2WT/WT mice. Neuronal iron uptake by DMT-1 is essential for normal hippocampal neuronal development and Slc11a2 expression is induced by spatial memory training. Deletion of Slc11a2 disrupts hippocampal neuronal development and spatial memory behavior.


* To whom correspondence should be addressed. E-mail: georg001{at}umn.edu.

Manuscript received 26 August 2008. Initial review completed 21 October 2008. Revision accepted 13 January 2009.

Published online 11 February 2009.







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