The ganglion cells of the mature retina project to the visual nuclei of the brain in a highly organized fashion. We have shown that during early development these projections are much less organized. This study will further characterize the optic projections in the immature visual system and investigate possible developmental mechanisms for the establishment and refinement of these early projections. There are five major lines of investigation. First, the degree of order between growing optic axons in the optic nerve, tract and tectum will be examined. This is to determine if there is sufficient order between ingrowing axons to account for the initial order in the terminal field. Second, the retinal ganglion cells giving rise to the earliest tectal projection will be identified. This is to evaluate the role fo temporal gradients in orienting the retinal map on the tectum. Third, timing will again be evaluated as a mechanism for determining the laminar distribution of ganglion cell axons in the tectum. This will involve determining the time and pattern of ingrowth of axons from the different ganglion cell classes to the tectum. Fourth, we will determine whether cell death is responsible for removing aberrantly projecting ganglion cells from the developing retina or if these cells can retract their aberrant collaterals. This will require labeling aberrantly projecting cells early in development and determining whether these labeled cells survive through the development of the visual system. Fifth, we will further characterize the role of the central visual nuclei in developmental cell death in the retina. This will involve attempts to alter the cell death in the ganglion cell layer by increasing the size of the tectum and attempts to demonstrate a specific trophic action of the tectum on retina.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY005371-03
Application #
3260411
Study Section
Visual Sciences B Study Section (VISB)
Project Start
1983-09-01
Project End
1987-04-30
Budget Start
1985-05-01
Budget End
1987-04-30
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
Schools of Medicine
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Wu, H H; Williams, C V; McLoon, S C (1994) Involvement of nitric oxide in the elimination of a transient retinotectal projection in development. Science 265:1593-6
Williams, C V; Nordquist, D; McLoon, S C (1994) Correlation of nitric oxide synthase expression with changing patterns of axonal projections in the developing visual system. J Neurosci 14:1746-55
Williams, C V; Stechmann, C L; McLoon, S C (1992) Subtractive immunization techniques for the production of monoclonal antibodies to rare antigens. Biotechniques 12:842-7
Williams, C V; McLoon, S C (1991) Elimination of the transient ipsilateral retinotectal projection is not solely achieved by cell death in the developing chick. J Neurosci 11:445-53
McLoon, S C (1991) A monoclonal antibody that distinguishes between temporal and nasal retinal axons. J Neurosci 11:1470-7
Nordquist, D; McLoon, S C (1991) Morphological patterns in the developing vertebrate retina. Anat Embryol (Berl) 184:433-40
McLoon, S C; Barnes, R B (1989) Early differentiation of retinal ganglion cells: an axonal protein expressed by premigratory and migrating retinal ganglion cells. J Neurosci 9:1424-32
McLoon, S C; McLoon, L K; Palm, S L et al. (1988) Transient expression of laminin in the optic nerve of the developing rat. J Neurosci 8:1981-90
Rogers, S L; Edson, K J; Letourneau, P C et al. (1986) Distribution of laminin in the developing peripheral nervous system of the chick. Dev Biol 113:429-35
McLoon, S C (1986) Response of astrocytes in the visual system to Wallerian degeneration: an immunohistochemical analysis of laminin and glial fibrillary acidic protein (GFAP). Exp Neurol 91:613-21

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