The axons of newly born neurons extend long distances before reaching their targets in the vertebrate brain. Pioneering retinal ganglion cell (RGC) axons in Xenopus laevis make this 450 Mum journey unerringly through a variety of cellular terrains. How are these early axons guided? The present proposal specifically addresses this question by investigating the interactions of the tips of RGC axons with their microenvironment as they pioneer the pathway. The experiments propose three main lines of investigation: 1) Light and electron microscopy of dye-filled RGC axons will be used to characterize the morphology and the microenvironment of pioneering growth cones at different stages of their advancement along the optic pathway. 2) Intracellular injection of Lucifer Yellow into RGCs will reveal whether their growth comes become dye-coupled to other cells in the pathway. If such coupling does occur, antibodies that specifically block gap junctional conductance will be used to test whether intercellular communication is necessary for axonal navigation. 3) To find out when the embryonic nervous system first becomes permissive to axonal pathfinding, eye primordia will be transplanted to progressively younger embryos. The earliest stage that directed axonal growth is supported will be determined and it will be asked whether specific guidance structures, identified ultrastructurally or immunologically, are associated with the onset of these permissive conditions. These experiments will provide a better understanding of the factors that influence the behavior of growing axons in vivo and help to define the cellular basis of axonal navigation in the embryonic CNS.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS023780-02
Application #
3407652
Study Section
Neurology B Subcommittee 1 (NEUB)
Project Start
1986-09-01
Project End
1990-08-31
Budget Start
1988-09-01
Budget End
1989-08-31
Support Year
2
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Type
Schools of Arts and Sciences
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
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Holt, C E; Harris, W A (1998) Target selection: invasion, mapping and cell choice. Curr Opin Neurobiol 8:98-105
Lom, B; Hopker, V; McFarlane, S et al. (1998) Fibroblast growth factor receptor signaling in Xenopus retinal axon extension. J Neurobiol 37:633-41
Worley, T L; Cornel, E; Holt, C E (1997) Overexpression of c-src and n-src in the developing Xenopus retina differentially impairs axonogenesis. Mol Cell Neurosci 9:276-92
Walz, A; McFarlane, S; Brickman, Y G et al. (1997) Essential role of heparan sulfates in axon navigation and targeting in the developing visual system. Development 124:2421-30
Worley, T L; Holt, C E (1996) Expression and herbimycin A-sensitive localization of pp125FAK in retinal growth cones. Neuroreport 7:1133-7
Burns, J C; McNeill, L; Shimizu, C et al. (1996) Retrovirol gene transfer in Xenopus cell lines and embryos. In Vitro Cell Dev Biol Anim 32:78-84
Worley, T; Holt, C (1996) Inhibition of protein tyrosine kinases impairs axon extension in the embryonic optic tract. J Neurosci 16:2294-306
McFarlane, S; Cornel, E; Amaya, E et al. (1996) Inhibition of FGF receptor activity in retinal ganglion cell axons causes errors in target recognition. Neuron 17:245-54
Riehl, R; Johnson, K; Bradley, R et al. (1996) Cadherin function is required for axon outgrowth in retinal ganglion cells in vivo. Neuron 17:837-48

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