The proposed studies will examine the mechanisms by which retinal projection neurons make precise and functional connections with their central targets. The hypothesis that neurotrophic factors modulate optic axon arborization, and synapse formation and stabilization will be tested in the live developing brain. Specifically, the cellular and molecular mechanisms by which the neurotrophin brain-derived neurotrophic factor (BDNF) controls axon and dendritic arborization, and synapse formation/stabilization will be examined in live, anesthetized tadpoles. The Xenopus laevis visual system offers a uniquely accessible vertebrate model in which the development of neuronal connections can be followed over time in the intact embryo. Embryologic manipulations and in vivo imaging techniques (time-lapse confocal microscopy and calcium imaging techniques) will be combined to follow, in real time, the morphological differentiation of pre- and post-synaptic partners and the formation of synaptic connections between the retina and its target optic tectum. By imaging individual optic axon terminal arbors and/or tectal neuron dendritic arbors while simultaneously visualizing synaptic sites in the intact animal, the following hypotheses will be tested: ? ? BDNF modulates activity-dependent competition between developing retinal inputs by promoting synapse stabilization between optic axons and target tectal neurons. ? ? Target-derived BDNF directly influences optic axon terminals to modulate axon arborization and synapse formation. The BDNF-elicited changes in optic axon arbor complexity lead to structural changes in tectal neuron synaptic complexity. ? ? BDNF induces localized changes in intracellular calcium levels in arborizing optic axons that are responsible for synapse stabilization and the formation of new branches. ? ? The results of these studies will provide valuable insights into fundamental mechanisms of synaptogenesis in the living brain, and will further our understanding of the mechanisms that control the development of visual pathways, that are critically important in the maintenance of normal visual function.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY011912-07
Application #
6658951
Study Section
Visual Sciences B Study Section (VISB)
Program Officer
Oberdorfer, Michael
Project Start
1998-08-01
Project End
2006-07-31
Budget Start
2003-08-01
Budget End
2004-07-31
Support Year
7
Fiscal Year
2003
Total Cost
$303,000
Indirect Cost
Name
University of California Irvine
Department
Other Basic Sciences
Type
Schools of Arts and Sciences
DUNS #
046705849
City
Irvine
State
CA
Country
United States
Zip Code
92697
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Igarashi, Miki; Santos, Rommel A; Cohen-Cory, Susana (2015) Impact of maternal n-3 polyunsaturated fatty acid deficiency on dendritic arbor morphology and connectivity of developing Xenopus laevis central neurons in vivo. J Neurosci 35:6079-92
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Manitt, Colleen; Nikolakopoulou, Angeliki M; Almario, David R et al. (2009) Netrin participates in the development of retinotectal synaptic connectivity by modulating axon arborization and synapse formation in the developing brain. J Neurosci 29:11065-77
Cohen-Cory, Susana (2008) Spatially patterned gradients of synaptic connectivity are established early in the developing retina. J Biol 7:15
Sanchez, Analiza L; Matthews, Benjamin J; Meynard, Margarita M et al. (2006) BDNF increases synapse density in dendrites of developing tectal neurons in vivo. Development 133:2477-86

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