ERKMEM
Erk1/2 SIGNALING IN MEMORY CONSOLIDATION AND ALLOCATION
| Coordinatore | UNIVERSITAT DE BARCELONA
Organization address
address: GRAN VIA DE LES CORTS CATALANES 585 contact info |
| Nazionalità Coordinatore | Spain [ES] |
| Totale costo | 87˙500 € |
| EC contributo | 87˙500 € |
| Programma | FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) |
| Code Call | FP7-PEOPLE-2013-CIG |
| Funding Scheme | MC-CIG |
| Anno di inizio | 2014 |
| Periodo (anno-mese-giorno) | 2014-03-01 - 2017-08-31 |
Partecipanti
| # | ||||
|---|---|---|---|---|
| 1 |
UNIVERSITAT DE BARCELONA
Organization address
address: GRAN VIA DE LES CORTS CATALANES 585 contact info |
ES (BARCELONA) | coordinator | 87˙500.00 |
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Obiettivo del progetto (Objective)
'The growing aging population of the EU predicts a steady increase in the health and economic burden of mental decline. Hence, the study of the molecular basis of long-term memory formation is a central topic in neuroscience with forseeable social implications. The Erk1/2 MAPK signaling pathway has been strongly implicated in the consolidation of episodic, hippocampus-dependent memories, and it also supports lasting forms of neuroplasticity. However, knowledge on neuronal Erk1/2 signaling is largely limited to mechanisms of activation. If left unchecked, Erk1/2 activation can be detrimental to cognition. It is therefore crucial to understand what intracellular processes rapidly inactivate Erk1/2 following stimulation by synaptic activity, and how they contribute to memory endurance and precision. Furthermore, although Erk1/2 couples to CREB activation, the role of CREB-mediated transcription in memory allocation is poorly defined. It is also not known how the multiple synaptic inputs innervating the hippocampus support memory-associated MAPK signaling. I propose to implement a multidisciplinary approach that will experimentally address these related gaps. We will explore novel forms of Erk1/2 regulation, from the role of tyrosine phosphatases to afferent neural projections and cellular ensembles. To achieve these goals, we will use a combination of transgenic mice, viral vectors for opto- and chemo-genetics, behavioral assays, biochemistry, and confocal imaging. These studies will yield basic insights into molecular mechanisms of memory and hippocampal physiology.'
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