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Investigating NMDA Receptor Contributions to Postsynaptic Potentials, Synaptic Integration and Hippocampal Network Dynamics

Project description

Rethinking brain signals for better health

When communication between brain cells falters, the consequences can be devastating, ranging from epilepsy and intellectual disability to speech impairments and psychiatric illnesses. Mutations in the GRIN2A gene, which encodes a subunit of the vital NMDA receptor, have been linked to these disorders. Yet, the precise mechanisms behind this dysfunction remain unclear. Supported by the Marie Skłodowska-Curie Actions programme, the Syn-to-Sum project is challenging long-held assumptions about how these receptors shape brain activity. Using genetically modified rat models, advanced electrophysiology, and calcium imaging, the project investigates how GluN2A subunit loss affects signal timing and processing in the hippocampus (the brain’s memory centre). By decoding this link, Syn-to-Sum aims to improve the futures for those living with GRIN2A-related conditions.

Objective

N-Methyl-D-Aspartate (NMDA) receptors, play a critical role in synaptic plasticity and are linked to various neurological disorders. Recent advancements in genetic sequencing have identified numerous variants in the GRIN2A gene, encoding the NMDAR receptor subunit GluN2A, to be associated with severe clinical outcomes, including intellectual disability, epileptic encephalopathy, speech and language impairments, and psychiatric illness. Yet, the specific mechanisms underlying the pathophysiology in these conditions remains elusive. Effective neuronal communication hinges on the precise coordination of synaptic signals. Conventionally, it is believed that the slow decay of NMDA receptor-mediated excitatory postsynaptic currents (EPSCs), is crucial for temporal summation and synaptic integration. However, my preliminary evidence from a Grin2a-depleted rat model challenges this view, suggesting that NMDA receptors do not contribute to the excitatory post synaptic potentials (EPSPs) of hippocampal pyramidal cells under physiological conditions. As such, this project seeks to further explore the impact of GluN2A depletion on temporal summation in inhibitory hippocampal cell populations. I will combine advanced electrophysiological techniques with ex vivo calcium imaging to assess how channel kinetics influence neuronal function, circuit plasticity and hippocampal network dynamics. Through this research, I aim to deepen our understanding of synaptic function, NMDA receptor physiology and the role of GluN2 subunit-conferred kinetics in neuronal computation and the sculpting of hippocampal network dynamics. By improving our understanding of how GRIN2A variants induce synaptic and network dysfunction, this research aims to provide novel insights into the pathogenesis of GRIN2A-associated disorders and identify novel targets for future development of targeted therapeutic interventions to improve the quality of life for affected individuals.

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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-2024-PF-01

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Coordinator

THE UNIVERSITY OF EDINBURGH
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.

€ 260 347,92
Address
OLD COLLEGE, SOUTH BRIDGE
EH8 9YL Edinburgh
United Kingdom

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Region
Scotland Eastern Scotland Edinburgh
Activity type
Higher or Secondary Education Establishments
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Total cost

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