Evidence map›Paper›PMID 41396684›Full record

ArticleeLife2025

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

Dario Cupolillo, Noelle Grosjean, Catherine Marneffe, Julio Viotti, Celia Reynaud, Severine Deforges, Mario Carta, Christophe Mulle

Abstract read
In one paragraph

Article in eLife, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Dario CupolilloInterdisciplinary Institute for Neuroscience, CNRS UMR 5297, University of Bordeaux, Bordeaux, France.
Noelle GrosjeanInterdisciplinary Institute for Neuroscience, CNRS UMR 5297, University of Bordeaux, Bordeaux, France.
Catherine MarneffeInterdisciplinary Institute for Neuroscience, CNRS UMR 5297, University of Bordeaux, Bordeaux, France.
Julio ViottiInterdisciplinary Institute for Neuroscience, CNRS UMR 5297, University of Bordeaux, Bordeaux, France.
Celia ReynaudInterdisciplinary Institute for Neuroscience, CNRS UMR 5297, University of Bordeaux, Bordeaux, France.
Severine DeforgesInterdisciplinary Institute for Neuroscience, CNRS UMR 5297, University of Bordeaux, Bordeaux, France.
Mario CartaInterdisciplinary Institute for Neuroscience, CNRS UMR 5297, University of Bordeaux, Bordeaux, France.
Christophe MulleInterdisciplinary Institute for Neuroscience, CNRS UMR 5297, University of Bordeaux, Bordeaux, France.ORCID https://orcid.org/0000-0003-2709-6615

Funding

Agence Nationale de la Recherche Hippencode 14-CE13-0015European Union MSCA ITN SYDAD 676144Fondation pour la Recherche Médicale FDT201904007898
6 · The paper itself

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 (PNs) 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 labeling 24 hr following a novel experience. Comparing FLEN+ and RAM+ neurons allows us 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 PNs 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 PNs undergo progressive plastic changes over the first day following a one-trial memory task.

Indexed as

CA3 Region, HippocampalPyramidal CellsStaining and LabelingAnimalsLearningMaleMemoryMiceMice, Inbred C57BLProto-Oncogene Proteins c-fosProto-Oncogene Proteins c-fosengramhippocampusintrinsic propertiesmemorymouseneurosciencesynapse

Identifiers

PMID41396684
PMCPMC12705066

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.