During embryonic development, vast numbers of neurons must form connections with their proper targets. Axons are guided to their targets by growth cones, which integrate and convert guidance signals into mechanical forces required for locomotion. Movement arises from dynamic regulation of cytoskeletal polymers and associated proteins. The Ena/VASP protein family functions in various axon guidance pathways and is known to regulate the assembly of actin filaments. Ena/VASP proteins are concentrated in the tips of growth cone filopodia, where the initial response to guidance signals occurs. Several signaling pathways implicated in axon guidance regulate Ena/VASP function. Therefore, Ena/VASP proteins are well positioned to act as key convergence points between signals from guidance pathways and the actin cytoskeleton. We will test the hypothesis that Ena/VASP proteins regulate actin remodeling in response to guidance signals. We propose to examine the role of Ena/VASP in growth cone guidance and translocation using high-resolution light and electron microscopy to analyze cytoskeletal dynamics and geometry. We will also employ genetic manipulation to perturb Ena/VASP function and biochemical approaches to study Ena/VASP's role in signaling pathways. This work should yield valuable insight into how the nervous system develops and how to design methods to repair it after injury.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM068678-03
Application #
6931627
Study Section
Molecular, Cellular and Developmental Neurosciences 2 (MDCN)
Program Officer
Rodewald, Richard D
Project Start
2003-08-01
Project End
2007-07-31
Budget Start
2005-08-01
Budget End
2006-07-31
Support Year
3
Fiscal Year
2005
Total Cost
$277,595
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Vidaki, Marina; Drees, Frauke; Saxena, Tanvi et al. (2017) A Requirement for Mena, an Actin Regulator, in Local mRNA Translation in Developing Neurons. Neuron 95:608-622.e5
McConnell, Russell E; Edward van Veen, J; Vidaki, Marina et al. (2016) A requirement for filopodia extension toward Slit during Robo-mediated axon repulsion. J Cell Biol 213:261-74
Menon, Shalini; Boyer, Nicholas Patrick; Winkle, Cortney Chelise et al. (2015) The E3 Ubiquitin Ligase TRIM9 Is a Filopodia Off Switch Required for Netrin-Dependent Axon Guidance. Dev Cell 35:698-712
Winkle, Cortney C; McClain, Leslie M; Valtschanoff, Juli G et al. (2014) A novel Netrin-1-sensitive mechanism promotes local SNARE-mediated exocytosis during axon branching. J Cell Biol 205:217-32
Pinheiro, Elaine M; Xie, Zhigang; Norovich, Amy L et al. (2011) Lpd depletion reveals that SRF specifies radial versus tangential migration of pyramidal neurons. Nat Cell Biol 13:989-95
Dent, Erik W; Gupton, Stephanie L; Gertler, Frank B (2011) The growth cone cytoskeleton in axon outgrowth and guidance. Cold Spring Harb Perspect Biol 3:
Hao, Joe C; Adler, Carolyn E; Mebane, Leslie et al. (2010) The tripartite motif protein MADD-2 functions with the receptor UNC-40 (DCC) in Netrin-mediated axon attraction and branching. Dev Cell 18:950-60
Gupton, Stephanie L; Gertler, Frank B (2010) Integrin signaling switches the cytoskeletal and exocytic machinery that drives neuritogenesis. Dev Cell 18:725-36
Menna, Elisabetta; Disanza, Andrea; Cagnoli, Cinzia et al. (2009) Eps8 regulates axonal filopodia in hippocampal neurons in response to brain-derived neurotrophic factor (BDNF). PLoS Biol 7:e1000138
Kwiatkowski, Adam V; Garner, Craig C; Nelson, W James et al. (2009) Cell autonomous defects in cortical development revealed by two-color chimera analysis. Mol Cell Neurosci 41:44-50

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