This competitive renewal grant is a request to support further analysis of age-related changes in membranes of human eye lens fiber-cells in order to elucidate major differences occurring in transparent and cataractous lenses. This proposal seeks to improve the methodology of membrane studies to the single lens level, which will allow us to consider donor health history information provided by the Eye Bank. The long-range goal is to understand the role of eye lens membranes in maintaining lens transparency. The lens membranes have unique lipid compositions and structures thought to maintain low oxygen concentration in the lens interior, and thus, protect against cataract formation. Our research will provide a basis to develop alternative strategies to prevent the onset or slow the progression of lens opacification. The emphasis will be on the role of the lipid bilayer portion of fiber-cell membranes in maintaining fiber-cell and lens homeostasis. Important progress in the previous grant period includes the identification of the role of cholesterol and the crucial role of cholesterol bilayer domains (CBDs) in particular. The presence of the CBD ensures that the surrounding phospholipid bilayer is saturated with cholesterol. The saturating cholesterol content in fiber-cell membranes keeps the bulk physical properties of lens-lipid membranes consistent and independent of changes in phospholipid composition. Thus, the CBD helps to maintain lens-membrane homeostasis while the membrane phospholipid composition changes significantly with age. We will (i) continue to adapt, refine, and improve our recently developed methods for the quantification of lipid domains in intact fiber-cell membranes to membranes derived from a single lens, and (ii) based on single lens measurements, examine changes in fiber-cell membranes occurring with age and cataract formation. Special attention will be paid to determine major differences in the organization of lipids in lens membranes of people with cataracts and age-matched clear lenses, as well as to the structure of lens membranes of people who retain clear lenses into their eighth and ninth decades. Finally (iii), we will test the hypothesis that an increase in oxygen tension in the lens (one of the causes of cataract formation) initiates lipid peroxidation and drastically changes the organization of lipids in fiber cell membranes, including the formation of CBDs and cholesterol crystals. Our studies will be based on the use of state-of-the-art EPR techniques and methods available and developed at the National Biomedical EPR Center at the Medical College of Wisconsin. EPR spin-labeling methods permit identification of membrane domains, give information about structure and molecular dynamics as a function of the membrane depth in coexisting domains, and allow quantification of lipids in these domains. They also are capable of measuring oxygen transport within and across membrane domains.

Public Health Relevance

Cataracts are a major cause of blindness throughout the world. At present surgery is the only effective treatment. The reason for the onset of cataracts is unknown, but a great deal of evidence suggests that the presence of high cholesterol and cholesterol bilayer domains in the eye lens helps to maintain transparency and prevent cataract formation. Our goal is to understand how fiber-cell plasma membranes in the lens, in particular their lipid bilayer portion, change during aging and cataract formation so that alternative strategies for preventing, slowing the progression, and curing cataracts can be devised and evaluated.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY015526-15
Application #
9709288
Study Section
Biology of the Visual System Study Section (BVS)
Program Officer
Araj, Houmam H
Project Start
2004-04-01
Project End
2020-05-31
Budget Start
2019-06-01
Budget End
2020-05-31
Support Year
15
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Medical College of Wisconsin
Department
Biophysics
Type
Schools of Medicine
DUNS #
937639060
City
Milwaukee
State
WI
Country
United States
Zip Code
53226
Plesnar, Elzbieta; Szczelina, Robert; Subczynski, Witold K et al. (2018) Is the cholesterol bilayer domain a barrier to oxygen transport into the eye lens? Biochim Biophys Acta Biomembr 1860:434-441
Mainali, Laxman; O'Brien, William J; Subczynski, Witold K (2018) Detection of cholesterol bilayer domains in intact biological membranes: Methodology development and its application to studies of eye lens fiber cell plasma membranes. Exp Eye Res 178:72-81
Subczynski, Witold Karol; Widomska, Justyna; Mainali, Laxman (2017) Factors Determining the Oxygen Permeability of Biological Membranes: Oxygen Transport Across Eye Lens Fiber-Cell Plasma Membranes. Adv Exp Med Biol 977:27-34
Mainali, Laxman; Raguz, Marija; O'Brien, William J et al. (2017) Changes in the Properties and Organization of Human Lens Lipid Membranes Occurring with Age. Curr Eye Res 42:721-731
Subczynski, Witold K; Mainali, Laxman; Raguz, Marija et al. (2017) Organization of lipids in fiber-cell plasma membranes of the eye lens. Exp Eye Res 156:79-86
Mainali, Laxman; Camenisch, Theodore G; Hyde, James S et al. (2017) Saturation recovery EPR spin-labeling method for quantification of lipids in biological membrane domains. Appl Magn Reson 48:1355-1373
Strangeway, Robert A; Hyde, James S; Camenisch, Theodore G et al. (2017) Broadband W-band Rapid Frequency Sweep Considerations for Fourier Transform EPR. Cell Biochem Biophys 75:259-273
Subczynski, Witold K; Pasenkiewicz-Gierula, Marta; Widomska, Justyna et al. (2017) High Cholesterol/Low Cholesterol: Effects in Biological Membranes: A Review. Cell Biochem Biophys 75:369-385
Widomska, Justyna; Subczynski, Witold K; Mainali, Laxman et al. (2017) Cholesterol Bilayer Domains in the Eye Lens Health: A Review. Cell Biochem Biophys 75:387-398
Zareba, M; Widomska, J; Burke, J M et al. (2016) Nitroxide free radicals protect macular carotenoids against chemical destruction (bleaching) during lipid peroxidation. Free Radic Biol Med 101:446-454

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