Neurons communicate through synapses, specialized junctions between presynaptic and postsynaptic neurons. Changes in synapse formation lead to altered synaptic plasticity and circuit formation, which can lead to changes in mood, behavior, and learning & memory. Additionally, some altered states, including disease and drug addiction, arise from alterations in synaptic efficacy. Recent work has identified cell adhesion molecules capable of inducing synapse formation. One of these is SynCAMI, the seminal member of the SynCAM family, which contains four related proteins. The objective of this proposal is to determine whether the individual SynCAMs have different synaptic induction properties and may thus contribute to a molecular code for synapse formation. The proposed studies are thus fundamental to understanding both the normal and diseased brain.
Three specific aims will be pursued to achieve this objective. In the first, the ability of the SynCAMs to induce presynaptic and postsynaptic terminals will be uncovered. In the second, the interactions between the SynCAMs that lead to this synapse induction will be determined in vitro. Here, the key question is to what extent each SynCAM preferentially interacts with itself or with others to induce a cellular response. In the third, these relationships between the SynCAMs will be tested in vivo. To address this aim, the localization of these molecules will first be determined. Then, the expression of each will be manipulated to determine whether specific synaptic types can be affected by perturbing SynCAM expression. In conclusion, these studies aim to elucidate fundamental mechanisms mediating induction and differentiation of synapses. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32DA021501-02
Application #
7494436
Study Section
Human Development Research Subcommittee (NIDA)
Program Officer
Babecki, Beth
Project Start
2007-09-01
Project End
2010-08-31
Budget Start
2008-09-01
Budget End
2009-08-31
Support Year
2
Fiscal Year
2008
Total Cost
$51,278
Indirect Cost
Name
Brown University
Department
Neurosciences
Type
Schools of Medicine
DUNS #
001785542
City
Providence
State
RI
Country
United States
Zip Code
02912
Akins, Michael R; Leblanc, Hannah F; Stackpole, Emily E et al. (2012) Systematic mapping of fragile X granules in the mouse brain reveals a potential role for presynaptic FMRP in sensorimotor functions. J Comp Neurol 520:3687-706
Christie, Sean B; Akins, Michael R; Schwob, James E et al. (2009) The FXG: a presynaptic fragile X granule expressed in a subset of developing brain circuits. J Neurosci 29:1514-24
Akins, Michael R; Berk-Rauch, Hanna E; Fallon, Justin R (2009) Presynaptic translation: stepping out of the postsynaptic shadow. Front Neural Circuits 3:17