Objective
Conditioned fear memory in response to an auditory stimulus serves as a prototype for studying the pathological emotional states as well as understanding the neural mechanisms of memory allocation, storage, retrieval and extinction. The conditioned fear memory in mice has been found to be allocated and stored within a subgroup of neurons in the amygdala, a critical region for expression of this type of memory. Expression levels of the transcription factor CREB (cyclic adenosine 3’-5’ monophospate response element –binding protein) has been shown to modulate allocation of memory to a specific group of neurons, constituting the memory trace, and neuronal excitability could play a role. Our goals in this proposal are, first, to investigate the synaptic properties in pairs of LA neurons before and after fear conditioning, and second, to delineate the neural mechanisms that allow a neuron to encode a specific memory and become part of the memory trace. In approaching our goals, we will conduct electrophysiological experiments in mice transfected with viral vectors that co-express CREB tagged with the green fluorescent protein (GFP) and the gene for channelrhodopsin2 (ChR2) allowing for specific activation of the transfected neurons. We will study the synaptic properties in pairs of transfected neurons by stimulating one neuron with a laser and performing whole-cell patch clamp recordings in another one. In addition, we will construct a network of amygdala neuron models based on experimental data which will allow us to simulate the emergence of plasticity changes observed in neurons that encode the same memory, and study the underlying biophysical mechanisms of these plasticity changes. The results from behavioral, electrophysiological and modeling experiments will give us insights on how neurons compete with each other for allocation to a specific memory.
Fields of science (EuroSciVoc)
CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques. See: The European Science Vocabulary.
CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques. See: The European Science Vocabulary.
- natural sciences biological sciences biochemistry biomolecules proteins
- natural sciences physical sciences optics laser physics
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Programme(s)
Multi-annual funding programmes that define the EU’s priorities for research and innovation.
Multi-annual funding programmes that define the EU’s priorities for research and innovation.
Topic(s)
Calls for proposals are divided into topics. A topic defines a specific subject or area for which applicants can submit proposals. The description of a topic comprises its specific scope and the expected impact of the funded project.
Calls for proposals are divided into topics. A topic defines a specific subject or area for which applicants can submit proposals. The description of a topic comprises its specific scope and the expected impact of the funded project.
Call for proposal
Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.
Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.
FP7-PEOPLE-2009-IOF
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Funding Scheme
Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.
Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.
Coordinator
700 13 IRAKLEIO
Greece
The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.