Guided migration of axons is an important conserved feature of neuronal development. Precise regulation of cytoskeletal dynamics is critical for proper axonal motility and guidance. Many known signaling proteins contribute to cytoskeletal remodeling, but it is not yet understood how their activities are coordinated during turning responses. Aplysia neuronal growth cones turn towards substrate-coated beads, requiring actin polymerization and signaling by Src. Preliminary data indicates that Src and its substrate, the Rho GTPase inhibitor p190RhoGAP colocalize to the bead target site along with Rac GTPase early in the response. Potentially, Src/GTPase signaling coordinates a biphasic switch during turning responses from a polymerizing/noncontractile early phase characterized by high Rac activity / low Rho activity, to a high Rac / high Rho contractile phase. To test this hypothesis, I propose to 1) establish whether Rho and Rac GTPase activities are spatially coordinated into segregated domains using GFP-conjugated biosensors and a newly designed solvent-sensitive Rho biosensor and 2) correlate temporal changes in the spatial distributions of GTPase activities with cytoskeletal dynamic remodeling as visualized with TIRF-FSM. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32NS054487-02
Application #
7350892
Study Section
Special Emphasis Panel (ZRG1-F03A-M (20))
Program Officer
Riddle, Robert D
Project Start
2007-02-01
Project End
2010-01-31
Budget Start
2008-02-01
Budget End
2009-01-31
Support Year
2
Fiscal Year
2008
Total Cost
$51,278
Indirect Cost
Name
Yale University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Buck, Kenneth B; Schaefer, Andrew W; Schoonderwoert, Vincent T et al. (2017) Local Arp2/3-dependent actin assembly modulates applied traction force during apCAM adhesion site maturation. Mol Biol Cell 28:98-110