Synaptic connectivity -- that is, synapse number and strength -- determines the computational power of neural networks. This begs the question; how are synaptic connections made, maintained and modified to accomplish the computational power of the mammalian brain? To address this question, I will image presynaptic proteins tagged with the green fluorescent protein (GFP), and its photoactivatable derivative (paGFP), in vivo and measure the following fundamental parameters as a function of development and experience: 1) How do axons branch and what fraction of new axonal branches are maintained into adulthood? 2) What fraction of presynaptic terminals formed during development are maintained into adulthood? 3) Does synaptic activity correlate with synaptic maintenance? These experiments will represent firsts in the characterization of cortical neurons in vivo during development and in the tracking of individual protein populations in vivo -- methodologies which will bridge the gap between molecular and cellular neurophysiology.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32NS053066-01
Application #
6994085
Study Section
Special Emphasis Panel (ZRG1-F03A (20))
Program Officer
Talley, Edmund M
Project Start
2005-07-01
Project End
2008-06-30
Budget Start
2005-07-01
Budget End
2006-06-30
Support Year
1
Fiscal Year
2005
Total Cost
$49,928
Indirect Cost
Name
Cold Spring Harbor Laboratory
Department
Type
DUNS #
065968786
City
Cold Spring Harbor
State
NY
Country
United States
Zip Code
11724