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Fundamental Themes in Neuroscience Seminar - Suzanne Paradis PhD

January 23, 2014 - 12:00pm to 1:00pm
Clark Center Auditorium

Suzanne Paradis, PhD, Biology Department, Brandeis University

"Signaling pathways that instruct rapid changes in neuronal connectivity"

Website: Paradis lab Web Site

A conversation with Suzanne Paradis with the Stanford group Neuwrite West can be streamed or downloaded here: Paradis conversation

Abstract:

The overall structure and function of circuits in the central nervous system is established by a variety of carefully orchestrated processes, including the formation of synapses and the morphogenesis of the dendritic arbor of individual neurons. Further, while it is well-established that sensory experience sculpts connections in the nervous system, it is not at all understood how this is accomplished at the molecular level. My lab focuses on identifying and defining the function of genes that regulate neuronal connectivity and structural plasticity both in the context of changes in sensory experience and nervous system development. We recently discovered that the activity-dependent expression of the GTPase Rem2 functions as a critical regulator of activity-dependent dendritic branching, as dialing Rem2 expression up or down in the context of increased sensory experience in an intact circuit decreases or increases dendritic branching accordingly. Overall, our studies of Rem2 reveal a previously unappreciated signaling paradigm whereby increased neuronal activity simultaneously initiates signal transduction networks that either promote or restrict dendritic arborization. In addition, our studies of synapse formation revealed that treatment of cultured neurons with the extracellular domain of the protein Sema4D causes a rapid increase (i.e. within 2 hours) in the density of functional GABAergic synapses. Using an organotypic hippocampal slice culture as an in vitro model of epileptiform activity, we demonstrated that acute Sema4D treatment rapidly and dramatically alters the hyperexcitability found in these slices in a manner consistent with a Sema4D-mediated increase in network inhibition. Our studies suggest the tantalizing possibility that Sema4D, as well as other molecules that instruct formation of GABAergic synapses, could be used as a disease-modifying treatment for epilepsy.

Recent Papers:

[1] Ghiretti, A.E., Kenny, K., Marr, M.T.2nd and Paradis, S. 2013. CaMKII-dependent phosphorylation of the GTPase Rem2 is required to restrict dendritic complexity. J Neurosci. 33(15):6504-15.

[2] Kuzirian, M., Moore, A. R., Staudenmaier, E., Friedel, R.H., and Paradis, S. 2013. The class 4 Semaphorin Sema4D promotes the rapid assembly of GABAergic synapses in rodent hippocampus. J Neurosci. 33: 8961-73. PMCID PMC3666179

Event Sponsor: 
Stanford Neurosciences Institute
Contact Email: 
ksn@stanford.edu
Contact Phone: 
650-498-7454

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