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Interneurons GATing of aversivE or rewarding information from the basolateral amygdala to ventral hippocampus.

Project description

Understanding how neuronal networks store and process information

Neuronal networks rely on inhibitory interneurons (INs) to process and store information. However, our understanding of how INs connect with pyramidal cells and engram cells, which encode memories, remains limited. With support from the Marie Skłodowska-Curie Actions programme, the InGATE project will focus on specific circuits in the amygdala and hippocampus related to valence coding. In this context, memories with negative or positive emotions are stored in different engram cells in the basolateral amygdala (BLA). The project will investigate how two subclasses of inhibitory neurons (parvalbumin (PV) and somatostatin (SST) expressing neurons) regulate the flow of aversive or rewarding information from the BLA to the CA1 region of the ventral hippocampus.

Objective

The ability of neuronal networks to process and store information relies on the activity of diverse subclasses of inhibitory interneurons (INs). While the importance of inhibition in controlling key features of network function is being increasingly appreciated, the understanding of the role of INs in neuronal networks function is limited by the incomplete knowledge of the connectivity between the different IN subclasses and pyramidal cells. Such gap of knowledge is even more evident when considering the connectivity between INs and engram cells, i.e. subgroups of pyramidal neurons encoding specific memories. In this conceptual framework, the InGATE project will analyze specific amygdalo-hippocampal circuits involved in valence coding, where memories of stimuli imbued with negative or positive valence segregate in different engram cells in the BLA. InGATE will test the hypothesis that two broad INs subclasses, the parvalbumin (PV) and somatostatin (SST) expressing INs, differentially gate aversive or rewarding information from the BLA to the CA1 region of the ventral hippocampus. To this end, I will analyze the functional connectivity between BLA aversive or rewarding engram cells (formed during fear or reward conditioning) to pyramidal cells and PV/SST interneurons in vCA1. In parallel, I will study vCA3 Schaffer collaterals converging on those vCA1 pyramidal cells and PV/SST interneurons that receive inputs from the BLA aversive or rewarding engram cells. Thus, the ultimate goal of InGATE is to clarify how PV or SST interneurons shape engram cells in vCA1 by integrating valence-related information from BLA and multisensory contextual information from the vCA3 area. InGATE will combine several state-of-the-art methodological approaches to generate, identify and manipulate aversive or rewarding BLA engrams and isolate their targets in vCA1. In addition, it will exploit an in vivo approach to measure population activity of excitatory and inhibitory neurons in vCA1.

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Programme(s)

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Topic(s)

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Funding Scheme

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HORIZON-TMA-MSCA-PF-EF - HORIZON TMA MSCA Postdoctoral Fellowships - European Fellowships

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Call for proposal

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(opens in new window) HORIZON-MSCA-2023-PF-01

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Coordinator

FONDAZIONE ISTITUTO ITALIANO DI TECNOLOGIA
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 188 590,08
Address
VIA MOREGO 30
16163 GENOVA
Italy

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Region
Nord-Ovest Liguria Genova
Activity type
Research Organisations
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Total cost

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