Evidence map›Paper›PMID 20053920›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

Glycine release from radial cells modulates the spontaneous activity and its propagation during early spinal cord development.

Anne-Laure Scain, Hervé Le Corronc, Anne-Emilie Allain, Emilie Muller, Jean-Michel Rigo, Pierre Meyrand, Pascal Branchereau, Pascal Legendre

Open access · hybridAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Glycine encephalopathy.The Egyptian journal of neurology, psychiatry and neurosurgery · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Persistent Sodium Current Drives Excitability of Immature Renshaw Cells in Early Embryonic Spinal Networks.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  13. Glycine Promotes the Survival of a Subpopulation of Neural Stem Cells.Frontiers in cell and developmental biology · 2018
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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 at 5 institutions in 4 countries.

Anne-Laure ScainCentre National de la Recherche Scientifique, Unité Mixte de Recherche 7102, Université Pierre et Marie Curie, F-75005 Paris, France.
Hervé Le Corronc
Anne-Emilie Allain
Emilie Muller
Jean-Michel Rigo
Pierre Meyrand
Pascal Branchereau
Pascal Legendre
Centre National de la Recherche Scientifique · FRUnit of Functional and Adaptive Biology · FRCentre National pour la Recherche Scientifique et Technique (CNRST) · MAHasselt University · BESorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rhythmic electrical activity is a hallmark of the developing embryonic CNS and is required for proper development in addition to genetic programs. Neurotransmitter release contributes to the genesis of this activity. In the mouse spinal cord, this rhythmic activity occurs after embryonic day 11.5 (E11.5) as waves spreading along the entire cord. At E12.5, blocking glycine receptors alters the propagation of the rhythmic activity, but the cellular source of the glycine receptor agonist, the release mechanisms, and its function remain obscure. At this early stage, the presence of synaptic activity even remains unexplored. Using isolated embryonic spinal cord preparations and whole-cell patch-clamp recordings of identified motoneurons, we find that the first synaptic activity develops at E12.5 and is mainly GABAergic. Using a multiple approach including direct measurement of neurotransmitter release (i.e., outside-out sniffer technique), we also show that, between E12.5 and E14.5, the main source of glycine in the embryonic spinal cord is radial cell progenitors, also known to be involved in neuronal migration. We then demonstrate that radial cells can release glycine during synaptogenesis. This spontaneous non-neuronal glycine release can also be evoked by mechanical stimuli and occurs through volume-sensitive chloride channels. Finally, we find that basal glycine release upregulates the propagating spontaneous rhythmic activity by depolarizing immature neurons and by increasing membrane potential fluctuations. Our data raise the question of a new role of radial cells as secretory cells involved in the modulation of the spontaneous electrical activity of embryonic neuronal networks.

Indexed as

PeriodicityAnimalsCells, CulturedCHO CellsCricetinaeCricetulusFemaleGlycineMiceMotor NeuronsPregnancySpinal CordSynaptic PotentialsGlycine

Identifiers

PMID20053920
PMCPMC6632542
OpenAlexW2017255456

What OpenQuestion holds

Textmetadata
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.