The long term objectives of this proposal are to determine the anatomical relationships between the retina and various retinal targets and to elucidate the rules that determine the organization of the retinal optic fibers in the pathways that lead them to their targets. This information will be applied to regenerating optic nerve axons to determine how the regeneration process leads to recovery of visual function. Such information may assist in establishing the methods and conditions necessary to achieve central nervous system regeneration in species that do not have this ability. Experiments are designed to determine whether in fact regenerating optic nerve fibers by-pass incorrect termination zones to terminate only in correct loci. In the course of these experiments, it will be determined whether different sectors of the retina normally project to different non-tectal retinal targets and whether different morphological types of retinal ganglion cells project to different targets. Another aim is to characterize the morphology of retinal ganglion cells and to examine the retinal ganglion cells to determine which cell types in which part of the retina lead the regenerative process. The methods to be used are both light and electronmicroscopy of optic axons filled with cobaltous-lysine. The cobalt method is extremely sensitive and is capable of filling optic axons at all stages of regeneration. It is also effective for retrogradely filling retinal ganglion cell bodies and dendrites when applied to the optic nerve. Radioautography will serve to complement the cobaltous-lysine method. Determining the projection of specific parts of the retina will be accomplished by applying cobaltous-lysine to a small retinal cut or by ablating part of the retina and applying cobaltous-lysine to the surviving axons from the intact part of the retina.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
2R01EY003552-04A1
Application #
3257901
Study Section
Visual Sciences B Study Section (VISB)
Project Start
1981-08-01
Project End
1986-11-30
Budget Start
1985-09-30
Budget End
1986-11-30
Support Year
4
Fiscal Year
1985
Total Cost
Indirect Cost
Name
New York Medical College
Department
Type
Schools of Medicine
DUNS #
City
Valhalla
State
NY
Country
United States
Zip Code
10595
Springer, A D; Morel, K D; Wilson, B R (1990) Topographic disorganization of the optic tracts following long-term optic nerve regeneration: a quantitative image analysis study. J Comp Neurol 298:458-71
Springer, A D; Sabban, E L; Morel, K D et al. (1990) Enhanced labeling of mitotic retinal cells with an intraocular [3H]thymidine injection. Neurosci Lett 118:1-4
Springer, A D; Wilson, B R (1989) Light microscopic study of degenerating cobalt-filled optic axons in goldfish: role of microglia and radial glia in debris removal. J Comp Neurol 282:119-32
Springer, A D; Morel, K D; Grobman, S L et al. (1989) Axonal redirection at the dorsoventral intraretinal boundary. J Comp Neurol 283:405-14
Mednick, A S; Berk, M F; Springer, A D (1988) Asymmetric distribution of cells in the inner nuclear and cone mosaic layers of the goldfish retina. Neurosci Lett 94:241-6
Mednick, A S; Springer, A D (1988) Asymmetric distribution of retinal ganglion cells in goldfish. J Comp Neurol 268:49-59
Springer, A D; Mednick, A S (1986) Simple and complex retinal ganglion cell axonal rearrangements at the optic chiasm. J Comp Neurol 247:233-45
Springer, A D; Mednick, A S (1986) Retinotopic and chronotopic organization of goldfish retinal ganglion cell axons throughout the optic nerve. J Comp Neurol 247:221-32
Springer, A D; Mednick, A S (1986) Relationship of ocular pigmentation to the boundaries of dorsal and ventral retina in a nonmammalian vertebrate. J Comp Neurol 245:74-82
Springer, A D; Mednick, A S (1985) Retinofugal and retinopetal projections in the cichlid fish Astronotus ocellatus. J Comp Neurol 236:179-96

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