The broad goals of the proposed program are to study mechanisms involved in axonal pathfinding during development and regeneration. Of specific interest is the signaling that translates a chemorepellent's action on the growth cone into collapse. Our data indicate that generation of eicosanoids by 12/15-lipoxygenase is necessary and sufficient (at least partially) for semaphorin 3A-induced collapse. Other results suggest that synthesis of these eicosanoids is part of a cascade involving, upstream, cytosolic phospholipases A2 (cPLA/2) and, downstream, protein kinase C (PKC) and adhesion site proteins, whose phosphorylation may trigger adhesion site disassembly and detachment. In a series of cell biological studies we will test the hypothesis that this pathway regulates detachment of the growth cone periphery during collapse. Experiments will be focused on the effects of semaphorin 3A. In cultures of responsive neurons we will study growth structure and adhesion. In isolated growth cone preparations enriched in the semaphorin 3A receptor, neurophilin-1, we will analyze cPLA2 activation, eicosanoid synthesis and PKC stimulation, as well as phosphorylation of adhesion site proteins. These studies are expected (i) to provide new insights into the little understood signalling mechanisms activated by repellants and (ii) to establish a novel signalling pathway that is believed to trigger disassembly of growth cone adhesion sites. The analysis of the mechanisms of growth cone pathfinding and repulsion is fundamental to our understanding of nervous system development, and insight into the action of chemorepellants on growth cones is likely to reveal new options for promoting nerve regeneration in the adult CNS.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS041029-05
Application #
6825753
Study Section
Special Emphasis Panel (ZRG1-MDCN-1 (01))
Program Officer
Riddle, Robert D
Project Start
2000-12-01
Project End
2006-11-30
Budget Start
2004-12-01
Budget End
2006-11-30
Support Year
5
Fiscal Year
2005
Total Cost
$297,525
Indirect Cost
Name
University of Colorado Denver
Department
Biology
Type
Schools of Medicine
DUNS #
041096314
City
Aurora
State
CO
Country
United States
Zip Code
80045
Estrada-Bernal, Adriana; Sanford, Staci D; Sosa, Lucas J et al. (2012) Functional complexity of the axonal growth cone: a proteomic analysis. PLoS One 7:e31858
Sanford, Staci D; Yun, Bo Goen; Leslie, Christina C et al. (2012) Group IVA phospholipase Aýýý is necessary for growth cone repulsion and collapse. J Neurochem 120:974-84
Dupraz, Sebastián; Grassi, Diego; Bernis, María Eugenia et al. (2009) The TC10-Exo70 complex is essential for membrane expansion and axonal specification in developing neurons. J Neurosci 29:13292-301
Estrada-Bernal, Adriana; Gatlin, Jesse C; Sunpaweravong, Somkiat et al. (2009) Dynamic adhesions and MARCKS in melanoma cells. J Cell Sci 122:2300-10
Sanford, Staci D; Gatlin, Jesse C; Hokfelt, Tomas et al. (2008) Growth cone responses to growth and chemotropic factors. Eur J Neurosci 28:268-78
Hokfelt, Tomas; Stanic, Davor; Sanford, Staci D et al. (2008) NPY and its involvement in axon guidance, neurogenesis, and feeding. Nutrition 24:860-8
Gatlin, Jesse C; Estrada-Bernal, Adriana; Sanford, Staci D et al. (2006) Myristoylated, alanine-rich C-kinase substrate phosphorylation regulates growth cone adhesion and pathfinding. Mol Biol Cell 17:5115-30
Kraus, Damian M; Elliott, Gary S; Chute, Hilary et al. (2006) CSMD1 is a novel multiple domain complement-regulatory protein highly expressed in the central nervous system and epithelial tissues. J Immunol 176:4419-30
Wang, Xiaoxin X; Pfenninger, Karl H (2006) Functional analysis of SIRPalpha in the growth cone. J Cell Sci 119:172-83
Sosa, Lucas; Dupraz, Sebastian; Laurino, Lisandro et al. (2006) IGF-1 receptor is essential for the establishment of hippocampal neuronal polarity. Nat Neurosci 9:993-5

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