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bioRxiv · 10.1101/2024.11.29.625977

Early changes in the properties of CA3 engram cells explored with a novel viral tool

Cupolillo, D.·Grosjean, N.·Marneffe, C.·Viotti, J.·Reynaud, C.·Deforges, S.·Carta, M.·Mulle, C.
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Abstract

Forming new memories after a one-time experience requires initial encoding then consolidation over time. During learning, multimodal information converges onto the hippocampus, activating sparse neuronal assemblies which are thought to form a memory representation through concerted activity and synaptic interconnectivity. In this work, we use a novel tool for fast fluorescent labeling of engram neurons (FLEN). FLEN is based on c-Fos activity-dependent transient expression of a destabilized fluorescent marker ZsGreen1 rapidly after one-trial learning. With FLEN, we explore the electrophysiological properties of c-Fos activated CA3 pyramidal neurons a few hours following one-trial learning of an episodic-like memory. In parallel, we employ the Robust Activity Marker (RAM) system, which provides activity-dependent labelling 24 hours following a novel experience. Comparing FLEN+ and RAM+ neurons allows to characterize how the properties of neuronal assemblies evolve during an initial phase of consolidation. Whereas no difference was observed in the excitability of FLEN+ vs. FLEN-neurons, RAM+ neurons were more excitable than RAM-neurons. This suggests that CA3 pyramidal neurons recruited in an engram progressively acquire increased excitability as compared to neurons which were not activated by the one-trial contextual memory task. On the other hand, like RAM+ neurons, FLEN+ CA3 neurons show an increased number of excitatory inputs. Overall, with the FLEN strategy, we can show that both the intrinsic excitability and the synaptic properties of CA3 pyramidal neurons undergo progressive plastic changes over the first day following a one-trial memory task.

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Cupolillo, D., Grosjean, N., Marneffe, C., Viotti, J., Reynaud, C., Deforges, S., Carta, M., Mulle, C.. 2024-11-30. Early changes in the properties of CA3 engram cells explored with a novel viral tool. https://doi.org/10.1101/2024.11.29.625977

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