A key aspect of retinal physiology is the phagocytosis by the retinal pigmented epithelium of rod outer segment discs shed during the process of rod-renewal. Little is known of the molecular events associated with this process. We shall investigate the hypothesis that carbohydrate components on the membranes of these organelles are involved in recognition phenomena with the cells of the retinal pigmented epithelium as an aspect of their engulfment. Initially, we shall examine a model system of carbohydrate recognition by these cells by investigating their ability to carry out the process of adsorptive endocytosis of glycoproteins which differ in their carbohydrate composition. The biological tool for these studies will be the pigmented epithelium cell of the embryonic chick, maintained in culture; the target molecules will be a series of 125I-neoglycoproteins which differ in the type of carbohydrate present, as well as iodinated, purified lysosomal enzymes with established markers for their uptake by other cells. These studies may reveal the presence in the retinal pigment epithelial cell of recognition systems for the endocytosis of glycoproteins involving specific carbohydrates. The second phase of these studies will investigate the ability of the pigmented epithelium cell, in culture, to engulf bovine rod outer segments, disc membranes, and rhodopsin-liposomes, and the influence on this process of modifying their carbohydrates by chemical and enzymatic means. Special emphasis will be placed on the effect of modifying the carbohydrates of rhodopsin in these membranes. Biochemical, isotopic, and electron-microscopic techniques will be used to follow these reactions.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY003685-05
Application #
3258111
Study Section
(VID)
Project Start
1981-05-01
Project End
1987-04-30
Budget Start
1985-05-01
Budget End
1987-04-30
Support Year
5
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Case Western Reserve University
Department
Type
Schools of Medicine
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Kean, E L (1999) The dolichol pathway in the retina and its involvement in the glycosylation of rhodopsin. Biochim Biophys Acta 1473:272-85
Kean, E L (1993) Topography of basal and stimulated biosynthesis of GlcNAc-P-P-dolichol and (GlcNAc)2-P-P-dolichol: variation in effect of proteolysis. Biochim Biophys Acta 1168:321-9
Kean, E L (1992) Studies on the activation by dolichol-P-mannose of the biosynthesis of GlcNAc-P-P-dolichol and the topography of the GlcNAc-transferases concerned with the synthesis of GlcNAc-P-P-dolichol and (GlcNAc)2-P-P-dolichol: a review. Biochem Cell Biol 70:413-21
Prasad, A V; Plantner, J J; Kean, E L (1992) Effect of enzymatic deglycosylation on the regenerability of bovine rhodopsin. Exp Eye Res 54:913-20
Prasad, A V; Ju, J M; Plantner, J J et al. (1992) Reductively methylated, tritiated rhodopsin of high specific activity;a convenient sensitive tracer for use in the radioimmunoassay of rhodopsin. Curr Eye Res 11:267-73
Ju, J M; Kean, E L (1992) In vitro galactosylation of rhodopsin and opsin: kinetics, properties and characterization. Exp Eye Res 55:589-604
Kean, E L (1991) Topographical orientation in microsomal vesicles of the N-acetylglucosaminyltransferases which catalyze the biosynthesis of N-acetylglucosaminylpyrophosphoryldolichol and N-acetylglucosaminyl-N-acetylglucosaminylpyrophosphoryldolichol. J Biol Chem 266:942-6
Plantner, J J; Le, M L; Kean, E L (1991) Enzymatic deglycosylation of bovine rhodopsin. Exp Eye Res 53:269-74
Kean, E L (1991) Sialic acid activation. Glycobiology 1:441-7
Plantner, J J; Lentrichia, B B; Kean, E L (1988) Biogenesis and content of rhodopsin in the retina of the chick during development. Curr Eye Res 7:503-10

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