The generation of axon collateral branches is a fundamental aspect of the development of synaptic connectivity between neurons and their targets, and branching/sprouting is also involved in the recovery of the nervous system following injury. The protrusion of axonal filopodia is the first step in the initiation of a collateral branch. Filopodia that become invaded by axonal microtubules subsequently mature into collateral branches. In this proposal we seek to determine the mechanisms of the initiation of axonal filopodia and their maturation into nascent collateral branches. In the first period of support for this project, our studies have unveiled the earliest steps in the cytoskeletal dynamics underlying the formation of axonal filopodia. We demonstrated that axonal filopodia are formed from precursor structures that we term axonal F-actin patches. The competitive renewal application for this project is based on the novel observation of axonal microdomains of phosphoinositide 3-kinase (PI3K) activity that precede the formation of axonal filopodia, which is in turn dependent on PI3K activity. The studies we propose will advance the field by testing a specific hypothesis that merges the earliest signaling and cytoskeletal events underlying branch formation into a coherent model. Using in vitro and in vivo approaches we will test the hypothesis that localized axonal microdomains of PI3K activity orchestrate the formation of axonal F-actin patches through the recruitment and activity of the Rac1 GTPase, the F-actin nucleating system Arp2/3 and septin GTPases, resulting in the coordinated reorganization of the actin and microtubule cytoskeleton giving rise to collateral branches.

Public Health Relevance

Axon collaterals are fundamental in the establishment of neuronal connectivity patterns and contribute to the regenerative response of injured axons in the nervous system. We propose to test the hypothesis that localized axonal microdomains of phosphoinositide 3-kinase activity orchestrate the functions of Rac1, Arp2/3 and septins in the reorganization of the axonal cytoskeleton during the first steps in the formation of axon collateral branches.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
High Priority, Short Term Project Award (R56)
Project #
2R56NS048090-06A1
Application #
8088996
Study Section
Synapses, Cytoskeleton and Trafficking Study Section (SYN)
Program Officer
Riddle, Robert D
Project Start
2004-04-01
Project End
2012-06-30
Budget Start
2010-07-15
Budget End
2012-06-30
Support Year
6
Fiscal Year
2010
Total Cost
$385,000
Indirect Cost
Name
Drexel University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
002604817
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Gallo, Gianluca (2013) Mechanisms underlying the initiation and dynamics of neuronal filopodia: from neurite formation to synaptogenesis. Int Rev Cell Mol Biol 301:95-156
Greif, Karen F; Asabere, Nana; Lutz, Gordon J et al. (2013) Synaptotagmin-1 promotes the formation of axonal filopodia and branches along the developing axons of forebrain neurons. Dev Neurobiol 73:27-44
Hu, Jianli; Bai, Xiaobo; Bowen, Jonathan R et al. (2012) Septin-driven coordination of actin and microtubule remodeling regulates the collateral branching of axons. Curr Biol 22:1109-15
Spillane, Mirela; Ketschek, Andrea; Donnelly, Chris J et al. (2012) Nerve growth factor-induced formation of axonal filopodia and collateral branches involves the intra-axonal synthesis of regulators of the actin-nucleating Arp2/3 complex. J Neurosci 32:17671-89
Bowen, Jonathan R; Hwang, Daniel; Bai, Xiaobo et al. (2011) Septin GTPases spatially guide microtubule organization and plus end dynamics in polarizing epithelia. J Cell Biol 194:187-97
Spillane, Mirela; Ketschek, Andrea; Jones, Steven L et al. (2011) The actin nucleating Arp2/3 complex contributes to the formation of axonal filopodia and branches through the regulation of actin patch precursors to filopodia. Dev Neurobiol 71:747-58
DeMay, Bradley S; Bai, Xiaobo; Howard, Louisa et al. (2011) Septin filaments exhibit a dynamic, paired organization that is conserved from yeast to mammals. J Cell Biol 193:1065-81
Gallo, Gianluca (2011) The cytoskeletal and signaling mechanisms of axon collateral branching. Dev Neurobiol 71:201-20
Ketschek, Andrea; Gallo, Gianluca (2010) Nerve growth factor induces axonal filopodia through localized microdomains of phosphoinositide 3-kinase activity that drive the formation of cytoskeletal precursors to filopodia. J Neurosci 30:12185-97
Kilinc, Devrim; Gallo, Gianluca; Barbee, Kenneth A (2009) Mechanical membrane injury induces axonal beading through localized activation of calpain. Exp Neurol 219:553-61

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