Our proposed research deals with environmental light damage to the retina of normal mice and rats and of those undergoing various forms of inherited retinal degeneration. We will study the damaging effects of fluorescent lighting at illuminance levels often found in office and industrial work environments. Our research objectives are three-fold. First, we shall clarify the sequence of cytopathologic steps in light damage and explore the possible role of the retinal pigment epithelium and the interphotoreceptor matrix in the degenerative process. To do this we will define the subcellular changes by quantitative electron microscopy. In addition, we will carry out studies using histochemistry, immunocytochemistry, and autoradiography of protein metabolism and transport or diffusion of various sugars. Second, we will study two determinants of the severity of light damage: eye pigmentation and genetic factors. To assess the protective role of eye pigmentation, we will use quantitative morphlogical methods and coisogenic and congenic strains of animals. To characterize the recently described genetic factors that regulate the susceptibility of the retina to light damage, we will use classical genetic crosses and recombinant inbred strains of mice to determine a) whether resistance to light damage is imparted by a single-gene or polygenic factor, b) the genetic mode of inheritance, and c) the chromosomal localization of the gene(s). In addition, we will probe the cellular and molecular mechanisms of resistance to light damage by the use of experimental mouse chimeras and collaborative biochemical studies. Third, we will examine the potentially damaging effects of light on the rate and character of the inherited retinal degenerations in the nervous and Purkinje cell degeneration mutant mice and in the RCS rat with inherited retinal dystrophy.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY004753-07
Application #
3259221
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1983-04-01
Project End
1990-03-31
Budget Start
1989-04-01
Budget End
1990-03-31
Support Year
7
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
LaVail, M M; Gorrin, G M (1987) Protection from light damage by ocular pigmentation: analysis using experimental chimeras and translocation mice. Exp Eye Res 44:877-89
LaVail, M M; Gorrin, G M; Repaci, M A et al. (1987) Genetic regulation of light damage to photoreceptors. Invest Ophthalmol Vis Sci 28:1043-8
LaVail, M M; Gorrin, G M; Repaci, M A et al. (1987) Light-induced retinal degeneration in albino mice and rats: strain and species differences. Prog Clin Biol Res 247:439-54
LaVail, M M; Papermaster, D S; Bridges, C D et al. (1987) Absence of an inherited retinal degeneration in the WAG/Rij rat. Exp Eye Res 44:465-9
LaVail, M M; Gorrin, G M; Repaci, M A (1987) Strain differences in sensitivity to light-induced photoreceptor degeneration in albino mice. Curr Eye Res 6:825-34
LaVail, M M; Lawson, N R (1986) Development of a congenic strain of pigmented and albino rats for light damage studies. Exp Eye Res 43:867-9