Evidence map›Paper›PMID 39443498›Full record

ArticleNature communications2024

Sensory experience steers representational drift in mouse visual cortex.

Joel Bauer, Uwe Lewin, Elizabeth Herbert, Julijana Gjorgjieva, Carl E Schoonover, Andrew J P Fink, Tobias Rose, Tobias Bonhoeffer, Mark Hübener

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Changes in perceptual sampling contribute to representational drift.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Coordinated Representational Drift Across the Mouse Cortex.bioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Representational drift reflects ongoing balancing of stochastic changes by Hebbian learning.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Representational drift without synaptic plasticity.bioRxiv : the preprint server for biology · 2025
    Article
  14. 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

9 authors.

Joel Bauer *Max Planck Institute for Biological Intelligence, Martinsried, Germany. joel.bauer@ucl.ac.uk.ORCID 0000-0001-5858-166X
Uwe Lewin *Max Planck Institute for Biological Intelligence, Martinsried, Germany.ORCID 0009-0008-6388-7637
Elizabeth HerbertSchool of Life Sciences, Technical University of Munich, Freising, Germany.ORCID 0000-0002-5893-9657
Julijana GjorgjievaSchool of Life Sciences, Technical University of Munich, Freising, Germany.ORCID 0000-0001-7118-4079
Carl E SchoonoverMortimer B. Zuckerman Mind Brain Behavior Institute, Department of Neuroscience, Columbia University, New York, NY, USA.ORCID 0000-0002-6397-1010
Andrew J P FinkMortimer B. Zuckerman Mind Brain Behavior Institute, Department of Neuroscience, Columbia University, New York, NY, USA.ORCID 0000-0003-4191-3298
Tobias RoseMax Planck Institute for Biological Intelligence, Martinsried, Germany.ORCID 0000-0002-7156-4714
Tobias BonhoefferMax Planck Institute for Biological Intelligence, Martinsried, Germany.ORCID 0000-0001-7897-6634
Mark HübenerMax Planck Institute for Biological Intelligence, Martinsried, Germany. mark.huebener@bi.mpg.de.ORCID 0000-0001-8367-9132

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) 1188 03580EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 804824
6 · The paper itself

Abstract

Representational drift-the gradual continuous change of neuronal representations-has been observed across many brain areas. It is unclear whether drift is caused by synaptic plasticity elicited by sensory experience, or by the intrinsic volatility of synapses. Here, using chronic two-photon calcium imaging in primary visual cortex of female mice, we find that the preferred stimulus orientation of individual neurons slowly drifts over the course of weeks. By using cylinder lens goggles to limit visual experience to a narrow range of orientations, we show that the direction of drift, but not its magnitude, is biased by the statistics of visual input. A network model suggests that drift of preferred orientation largely results from synaptic volatility, which under normal visual conditions is counteracted by experience-driven Hebbian mechanisms, stabilizing preferred orientation. Under deprivation conditions these Hebbian mechanisms enable adaptation. Thus, Hebbian synaptic plasticity steers drift to match the statistics of the environment.

Indexed as

Neuronal PlasticityNeuronsVisual CortexAnimalsCalciumFemaleMiceMice, Inbred C57BLModels, NeurologicalOrientationPhotic StimulationPrimary Visual CortexSynapsesVisual PerceptionCalcium

Identifiers

PMID39443498
PMCPMC11499870

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.