Probably the most important part of the growing axon is the structure at its tip, the growth cone. Nerve growth cones are essential for directed axonal outgrowth. They are complex sensory-motor machines that respond to environmental cues through cell surface receptors or changes in ion channel permeability. They locally process this information using signal transduction pathways that regulate the motility mechanism responsible for driving forward advancement through the environment. Relatively little is known about the specific mechanisms that integrate the information and regulate its affect on motility. Although signal transduction pathways have been implicated, it has been difficult to link these pathways to specific effecter mechanisms of motility that persist over time. One effecter mechanism is the generation of force by myosin. Myosin activity has multiple roles that include the control of growth cone shape changes and the generation of traction force that drives forward advancement. It is an important effecter of growth cone motility that may be essential for changes in direction of advancement. My overall goal is to identify the various myosins responsible for modulating growth cone motility, understand how pathways that are stimulated by specific environmental cues control myosin activity and how the force that is developed is coupled to the extracellular environment to provide traction force. I propose that myosin II is the most important of the myosins identified in growth cones for regulating motility and producing traction force. I will test this proposal by eliminating the activity of myosin II and then measuring key aspects of motility including traction force. I also plan to identify the major pathways involved in growth cone myosin II regulation. Combined these results will provide the framework for understanding the molecular basis of growth cone motility and how environmental cues stimulate specific pathways to regulate this motility. This is essential for understanding the formation of neuronal circuitry during development and the mechanisms required for successful nerve regeneration.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
2R01NS026150-12A2
Application #
6613084
Study Section
Molecular, Cellular and Developmental Neurosciences 2 (MDCN)
Program Officer
Tagle, Danilo A
Project Start
1988-04-01
Project End
2008-01-31
Budget Start
2003-02-04
Budget End
2004-01-31
Support Year
12
Fiscal Year
2003
Total Cost
$254,363
Indirect Cost
Name
Washington University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Brown, Jacquelyn A; Wysolmerski, Robert B; Bridgman, Paul C (2009) Dorsal root ganglion neurons react to semaphorin 3A application through a biphasic response that requires multiple myosin II isoforms. Mol Biol Cell 20:1167-79
Kollins, K M; Hu, J; Bridgman, P C et al. (2009) Myosin-II negatively regulates minor process extension and the temporal development of neuronal polarity. Dev Neurobiol 69:279-98
Brown, Jacquelyn A; Bridgman, Paul C (2009) Disruption of the cytoskeleton during Semaphorin 3A induced growth cone collapse correlates with differences in actin organization and associated binding proteins. Dev Neurobiol 69:633-46
Goeckeler, Zoe M; Bridgman, Paul C; Wysolmerski, Robert B (2008) Nonmuscle myosin II is responsible for maintaining endothelial cell basal tone and stress fiber integrity. Am J Physiol Cell Physiol 295:C994-1006
Turney, Stephen G; Bridgman, Paul C (2005) Laminin stimulates and guides axonal outgrowth via growth cone myosin II activity. Nat Neurosci 8:717-9
Young, Michael E; Cooper, John A; Bridgman, Paul C (2004) Yeast actin patches are networks of branched actin filaments. J Cell Biol 166:629-35
Bridgman, Paul C (2004) Myosin-dependent transport in neurons. J Neurobiol 58:164-74
Brown, Michael E; Bridgman, Paul C (2003) Retrograde flow rate is increased in growth cones from myosin IIB knockout mice. J Cell Sci 116:1087-94
Bridgman, Paul C; Brown, Michael E; Balan, Irina (2003) Biolistic transfection. Methods Cell Biol 71:353-68
Bridgman, Paul C (2002) Growth cones contain myosin II bipolar filament arrays. Cell Motil Cytoskeleton 52:91-6

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