Evidence map›Paper›PMID 28826501›Full record

ArticleeLife2017

Electrical activity controls area-specific expression of neuronal apoptosis in the mouse developing cerebral cortex.

Oriane Blanquie, Jenq-Wei Yang, Werner Kilb, Salim Sharopov, Anne Sinning, Heiko J Luhmann

Abstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 1 pooled it
–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

67 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  7. Developmental and Early-Life Stress-Induced Effects on 5-HTbioRxiv : the preprint server for biology · 2025
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  15. Oligodendrocyte Maturation Alters the Cell Death Mechanisms That Cause Demyelination.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
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7 more citing papers are in PubMed but not listed here.

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

6 authors.

Oriane BlanquieInstitute of Physiology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.ORCID http://orcid.org/0000-0003-2361-7129
Jenq-Wei YangInstitute of Physiology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Werner KilbInstitute of Physiology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Salim SharopovInstitute of Physiology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Anne Sinning *Institute of Physiology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.ORCID http://orcid.org/0000-0002-1518-7272
Heiko J Luhmann *Institute of Physiology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.ORCID http://orcid.org/0000-0002-7934-8661

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Programmed cell death widely but heterogeneously affects the developing brain, causing the loss of up to 50% of neurons in rodents. However, whether this heterogeneity originates from neuronal identity and/or network-dependent processes is unknown. Here, we report that the primary motor cortex (M1) and primary somatosensory cortex (S1), two adjacent but functionally distinct areas, display striking differences in density of apoptotic neurons during the early postnatal period. These differences in rate of apoptosis negatively correlate with region-dependent levels of activity. Disrupting this activity either pharmacologically or by electrical stimulation alters the spatial pattern of apoptosis and sensory deprivation leads to exacerbated amounts of apoptotic neurons in the corresponding functional area of the neocortex. Thus, our data demonstrate that spontaneous and periphery-driven activity patterns are important for the structural and functional maturation of the neocortex by refining the final number of cortical neurons in a region-dependent manner.

Indexed as

ApoptosisElectrophysiological PhenomenaAgingAnesthesiaAnimalsAnimals, NewbornCaspase 3Cell CountCerebral CortexMiceMotor CortexNeuronsSomatosensory CortexCaspase 3activity patternsapoptosiscell deathcerebral cortexdevelopmentdevelopmental biologymouseneurosciencestem cellswhisker deafferentation

Identifiers

PMID28826501
PMCPMC5582867

What OpenQuestion holds

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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.