Evidence map›Paper›PMID 34723790›Full record

ArticleeLife2021

CA1 pyramidal cell diversity is rooted in the time of neurogenesis.

Davide Cavalieri, Alexandra Angelova, Anas Islah, Catherine Lopez, Marco Bocchio, Yannick Bollmann, Agnès Baude, Rosa Cossart

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.6field-weighted citation impact, top 7% of its field
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

32 citing papers in PubMed, 38 citations in OpenAlex.

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  13. A conserved logic for the development of cortical layering in tetrapods.bioRxiv : the preprint server for biology · 2025
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  17. Development of Differential Sublaminar Feedforward Inhibitory Circuits in CA1 Hippocampus RequiresThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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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

8 authors at 1 institution in 1 country.

Davide CavalieriAix Marseille Université, Inserm, INMED, Turing Center for Living Systems, Marseille, France.ORCID 0000-0003-2369-647X
Alexandra AngelovaAix Marseille Université, Inserm, INMED, Turing Center for Living Systems, Marseille, France.
Anas IslahAix Marseille Université, Inserm, INMED, Turing Center for Living Systems, Marseille, France.
Catherine LopezAix Marseille Université, Inserm, INMED, Turing Center for Living Systems, Marseille, France.
Marco BocchioAix Marseille Université, Inserm, INMED, Turing Center for Living Systems, Marseille, France.ORCID 0000-0002-7005-3453
Yannick BollmannAix Marseille Université, Inserm, INMED, Turing Center for Living Systems, Marseille, France.
Agnès BaudeAix Marseille Université, Inserm, INMED, Turing Center for Living Systems, Marseille, France.ORCID 0000-0002-7025-364X
Rosa CossartAix Marseille Université, Inserm, INMED, Turing Center for Living Systems, Marseille, France.ORCID 0000-0003-2111-6638
Inserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular diversity supports the computational capacity and flexibility of cortical circuits. Accordingly, principal neurons at the CA1 output node of the murine hippocampus are increasingly recognized as a heterogeneous population. Their genes, molecular content, intrinsic morpho-physiology, connectivity, and function seem to segregate along the main anatomical axes of the hippocampus. Since these axes reflect the temporal order of principal cell neurogenesis, we directly examined the relationship between birthdate and CA1 pyramidal neuron diversity, focusing on the ventral hippocampus. We used a genetic fate-mapping approach that allowed tagging three groups of age-matched principal neurons: pioneer, early-, and late-born. Using a combination of neuroanatomy, slice physiology, connectivity tracing, and cFos staining in mice, we show that birthdate is a strong predictor of CA1 principal cell diversity. We unravel a subpopulation of pioneer neurons recruited in familiar environments with remarkable positioning, morpho-physiological features, and connectivity. Therefore, despite the expected plasticity of hippocampal circuits, given their role in learning and memory, the diversity of their main components is also partly determined at the earliest steps of development.

Indexed as

NeurogenesisAnimalsCA1 Region, HippocampalFemaleMaleMicePyramidal CellsDevelopmentHippocampusmouseNeuronal diversityneurosciencePyramidal cell

Identifiers

PMID34723790
PMCPMC8660020
OpenAlexW3209905200

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.