Evidence map›Paper›PMID 38243089›Full record

ArticleNature neuroscience2024

Dynamic and selective engrams emerge with memory consolidation.

Douglas Feitosa Tomé, Ying Zhang, Tomomi Aida, Olivia Mosto, Yifeng Lu, Mandy Chen, Sadra Sadeh, Dheeraj S Roy, Claudia Clopath

Abstract read
In one paragraph

Article in Nature neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Article
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  6. Article
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  8. Article
  9. Reductionism in Engram Neuroscience.The European journal of neuroscience · 2026
    Review
  10. Review
  11. Article
  12. Modular inhibitory coding in binary networks.Frontiers in network physiology · 2026
    Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
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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

9 authors.

Douglas Feitosa Tomé *Department of Bioengineering, Imperial College London, London, UK. douglas.feitosatome@ist.ac.at.ORCID http://orcid.org/0000-0002-6535-8412
Ying Zhang *McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA. y_zhang@mail.tsinghua.edu.cn.ORCID http://orcid.org/0000-0001-6675-3273
Tomomi AidaMcGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA.ORCID http://orcid.org/0000-0003-2021-4439
Olivia MostoMcGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Yifeng LuCenter for Life Sciences & IDG/McGovern Institute for Brain Research, School of Life Sciences, Tsinghua University, Beijing, China.
Mandy ChenMcGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Sadra SadehDepartment of Bioengineering, Imperial College London, London, UK.
Dheeraj S RoyStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA. dsroy@buffalo.edu.ORCID http://orcid.org/0000-0002-5218-1216
Claudia ClopathDepartment of Bioengineering, Imperial College London, London, UK. c.clopath@imperial.ac.uk.ORCID http://orcid.org/0000-0003-4507-8648

Funding

Determining the Role of Distinct Parafascicular Thalamic Circuits in Motor Behaviors Relevant to Parkinson’s DiseaseK99NS125131 · NINDS · BROAD INSTITUTE, INC. · PI ROY, DHEERAJ · 2022 to 2023
$217k
NINDS NIH HHS K99 NS125131Wellcome Trust
6 · The paper itself

Abstract

Episodic memories are encoded by experience-activated neuronal ensembles that remain necessary and sufficient for recall. However, the temporal evolution of memory engrams after initial encoding is unclear. In this study, we employed computational and experimental approaches to examine how the neural composition and selectivity of engrams change with memory consolidation. Our spiking neural network model yielded testable predictions: memories transition from unselective to selective as neurons drop out of and drop into engrams; inhibitory activity during recall is essential for memory selectivity; and inhibitory synaptic plasticity during memory consolidation is critical for engrams to become selective. Using activity-dependent labeling, longitudinal calcium imaging and a combination of optogenetic and chemogenetic manipulations in mouse dentate gyrus, we conducted contextual fear conditioning experiments that supported our model's predictions. Our results reveal that memory engrams are dynamic and that changes in engram composition mediated by inhibitory plasticity are crucial for the emergence of memory selectivity.

Indexed as

Memory ConsolidationMemory, EpisodicAnimalsFearMental RecallMiceNeurons

Identifiers

PMID38243089
PMCPMC10917686

What OpenQuestion holds

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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.