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Mapping dEndritic inforMation prOcessing in behaving mice using simultaneous spatio-tempoRal voltage and calcium Imaging and wholE-cell electrophySiology

Project description

Learning about memory formation with unprecedented imaging in behaving mice

Unlike most other cells in the body, neurons have a very special morphology critical to signal processing. A highly branched and dynamically changing 'dendritic tree' receives many inputs from other cells, opening ion channels and creating rapid changes in voltage for long-term modifications in structure and function related to learning and memory. Other voltage changes within the neurons may also modulate signals but observing these intracellular dynamics in awake and behaving animals was not possible until recently. MEMORIES has developed a pioneering technique and is planning to apply it for the first time ever to behaving mice. The experiments promise unprecedented insight into the neurobiological substrates of learning and memory.

Objective

Dendritic information processing is fundamental to how we perceive and interact with the world around us. Spatio-temporal maps of dendritic voltage reveal how information is processed in the brain, but remain unexplored in awake animals, since no recording technique was previously available to study them.
I recently developed a novel technique for spatio-temporal mapping of dendritic processing in unparalleled detail (Roome and Kuhn, 2018). My pioneering experiments provided the first observation of spatio-temporal dendritic voltage signalling in vivo. For the first time, I combined simultaneous dendritic voltage and calcium imaging with somatic recording in cerebellar Purkinje neurons of awake mice to reveal complex dendritic processes, including discrete dendritic spikelets, back-propagating action potentials and localized subthreshold signalling.
Using my novel technique to record from neocortical Pyramidal neurons, I will now investigate dendritic processing in behaving mice, to explore how memories are formed during learning. I will focus on how back-propagating action potentials contribute to dendritic processing, through modulation of synaptic plasticity. The Laboratory of Sensory Processing (Prof. Carl Petersen) at EPFL, Switzerland, is specialized for investigating synaptic mechanisms of sensory processing and highly experienced in whole-cell recording and optical imaging during animal behaviour and training; all of which are critical for the success of this project.
This fellowship will be instrumental in propelling a technique, that I have been committed to developing, towards state-of-the-art research in neuroscience. It will provide an ideal avenue for introducing a new technique to Europe, through a world leading laboratory, and prove invaluable for sharing skills I acquired abroad, while establishing networks and collaborations as I re-integrate into the European neuroscience community, in pursuit of a professional research carrier based in Europe.

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Topic(s)

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Funding Scheme

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MSCA-IF - Marie Skłodowska-Curie Individual Fellowships (IF)

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Call for proposal

Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.

(opens in new window) H2020-MSCA-IF-2018

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Coordinator

ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE
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.

€ 203 149,44
Address
BATIMENT CE 3316 STATION 1
1015 LAUSANNE
Switzerland

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Region
Schweiz/Suisse/Svizzera Région lémanique Vaud
Activity type
Higher or Secondary Education Establishments
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Total cost

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.

€ 203 149,44
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