Several significant findings from this laboratory during the current funding period indicate that regulation of iron (Fe) availability is a crucial component of ocular homeostasis, and that availability of Fe may play a pivotal role in ocular pathology. In the current proposal, we plan to investigate these observations in greater detail and to elucidate the mechanisms involved in Fe storage in the lens in normal and pathological conditions. The hypothesis to be addressed is that lenticular uptake and storage of Fe is essential for ocular homeostasis under normal conditions. This ability is compromised in inflammation or cataractogenesis, resulting in increased lenticular Fe concentration. Deleterious changes in lenticular function then occur due to Fe-catalyzed oxidative reactions. Because of the demonstrated importance of Fe to ocular pathophysiology and because virtually nothing is presently known about ocular Fe homeostasis, experiments in this proposal are designed to fill this gap. These studies will begin with experiments using lens epithelial cell cultures and then will be extended to whole lens cultures and finally to the in vivo situation. Mechanisms for Fe transport and storage in the lens will be defined using both whole rabbit lenses and epithelial cell cultures from normal rabbit and canine lenses, and canine cataractous lenses. The limits of lenticular capacity for transport and storage of Fe will be determined. The effects of exceeding capacity on lens function and the mechanisms underlying these alterations will then be determined. Since the lens is likely to be an important regulator of ocular Fe homeostasis in vivo, the effects of aphakia on ocular Fe homeostasis in normal and inflamed eyes will be determined. The results of these experiments will provide essential information about lenticular Fe homeostasis and about the contributions of the lens to ocular Fe homeostasis. Detailed information about the functions of Fe in ocular pathology is likely to provide important insights for rational design of new and more effective therapeutic regimes.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY004900-11
Application #
3259507
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1986-04-01
Project End
1997-06-30
Budget Start
1993-07-01
Budget End
1994-06-30
Support Year
11
Fiscal Year
1993
Total Cost
Indirect Cost
Name
North Carolina State University Raleigh
Department
Type
Schools of Veterinary Medicine
DUNS #
City
Raleigh
State
NC
Country
United States
Zip Code
27695
Goralska, Malgorzata; Fleisher, Lloyd N; McGahan, M Christine (2017) Vitreous Humor Changes Expression of Iron-Handling Proteins in Lens Epithelial Cells. Invest Ophthalmol Vis Sci 58:1187-1195
Harned, Jill; Nagar, Steven; McGahan, M Christine (2014) Hypoxia controls iron metabolism and glutamate secretion in retinal pigmented epithelial cells. Biochim Biophys Acta 1840:3138-44
Goralska, Ma?gorzata; Fleisher, Lloyd N; McGahan, M Christine (2014) Hypoxia induced changes in expression of proteins involved in iron uptake and storage in cultured lens epithelial cells. Exp Eye Res 125:135-41
Lall, Marilyn M; Harned, Jill; McGahan, M Christine (2013) Hydrogen peroxide and extracellular signal-related kinase 1/2 pathway regulate ferritin levels in retinal pigmented and lens epithelial cells. Mol Vis 19:2106-12
Goralska, Ma?gorzata; Nagar, Steven; Fleisher, Lloyd N et al. (2013) Source-dependent intracellular distribution of iron in lens epithelial cells cultured under normoxic and hypoxic conditions. Invest Ophthalmol Vis Sci 54:7666-73
Harned, J; Ferrell, J; Nagar, S et al. (2012) Ceruloplasmin alters intracellular iron regulated proteins and pathways: ferritin, transferrin receptor, glutamate and hypoxia-inducible factor-1ýý. Exp Eye Res 97:90-7
Harned, Jill; Ferrell, Jenny; Lall, Marilyn M et al. (2010) Altered ferritin subunit composition: change in iron metabolism in lens epithelial cells and downstream effects on glutathione levels and VEGF secretion. Invest Ophthalmol Vis Sci 51:4437-46
Goralska, Malgorzata; Nagar, Steven; Colitz, Carmen M H et al. (2009) Changes in ferritin H- and L-chains in canine lenses with age-related nuclear cataract. Invest Ophthalmol Vis Sci 50:305-10
Goralska, M; Ferrell, J; Harned, J et al. (2009) Iron metabolism in the eye: a review. Exp Eye Res 88:204-15
Goralska, M; Nagar, S; Fleisher, L N et al. (2009) Distribution of ferritin chains in canine lenses with and without age-related nuclear cataracts. Mol Vis 15:2404-10