Genetic variants of the HFE gene are the leading cause of adult onset hereditary hemochromatosis (HH), the most common Mendelian genetic disease in the North American Caucasian population. The missense variants C282Y and H63D promote increased intestinal absorption and progressive tissue deposition of iron. HH has also been associated with derangements in the metabolism of other divalent metals, and it is thought these effects arise due to malregulation of divalent metal transporter (DMT1). Work in our laboratory has demonstrated that manganese can enter the central nervous system directly across the olfactory epithelium by a mechanism that involves DMT1. We therefore hypothesize that carriers of C282Y and/or H63D HFE alleles may be more susceptible to manganese exposure through the olfactory pathway, and consequently may have impaired olfactory function. Our model further suggests that Hfe-/- knockout mice would have increased 54Mn absorption through the olfactory system and that these animals would be more sensitive to manganese exposures causing impaired olfaction. This pilot project will test the hypothesis that HFE acts as a genetic determinant of olfactory manganese absorption and toxicity.

Public Health Relevance

Genetic variants of the HFE gene are the leading cause of adult onset hereditary hemochromatosis (HH), the most common Mendelian genetic disease in the North American Caucasian population. The missense variants C282Y and H63D promote increased intestinal absorption and progressive tissue deposition of iron. Our hypothesis is that HFE acts as a genetic determinant of olfactory manganese absorption and toxicity. To test this hypothesis, we will study a mouse model of HFE-associated hemochromatosis to test whether absorption of inhaled manganese is altered, and whether HFE therefore promotes a greater susceptibility to damage to olfaction - the sense of smell.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Small Research Grants (R03)
Project #
5R03DA027030-02
Application #
7941943
Study Section
Special Emphasis Panel (ZDA1-GXM-A (03))
Program Officer
Wideroff, Louise
Project Start
2009-09-30
Project End
2012-08-31
Budget Start
2010-09-01
Budget End
2012-08-31
Support Year
2
Fiscal Year
2010
Total Cost
$161,865
Indirect Cost
Name
Harvard University
Department
Genetics
Type
Schools of Public Health
DUNS #
149617367
City
Boston
State
MA
Country
United States
Zip Code
02115
Kim, Jonghan; Buckett, Peter D; Wessling-Resnick, Marianne (2013) Absorption of manganese and iron in a mouse model of hemochromatosis. PLoS One 8:e64944
Byrne, Shaina L; Krishnamurthy, Divya; Wessling-Resnick, Marianne (2013) Pharmacology of iron transport. Annu Rev Pharmacol Toxicol 53:17-36
Kim, Jonghan; Li, Yuan; Buckett, Peter D et al. (2012) Iron-responsive olfactory uptake of manganese improves motor function deficits associated with iron deficiency. PLoS One 7:e33533
Claus Henn, Birgit; Kim, Jonghan; Wessling-Resnick, Marianne et al. (2011) Associations of iron metabolism genes with blood manganese levels: a population-based study with validation data from animal models. Environ Health 10:97
Wessling-Resnick, Marianne (2010) Iron homeostasis and the inflammatory response. Annu Rev Nutr 30:105-22