Evidence map›Paper›PMID 24259577›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2013

Functional subpopulations of V3 interneurons in the mature mouse spinal cord.

Joanna Borowska, Christopher T Jones, Han Zhang, Jake Blacklaws, Martyn Goulding, Ying Zhang

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing 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

70 citing papers in PubMed.

  1. Gene expression programs underlying spinal commissural neuron differentiation and axon growth across the midline.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. A spinal substrate for modular control of natural behavior.bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Excitatory Spinal Lhx9-Derived Interneurons Modulate Locomotor Frequency in Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Excitatory and Inhibitory Descending Commissural Interneurons Differentially Integrate Supraspinal and Segmental Sensory Signals.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  20. Article

10 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.

Joanna BorowskaDepartments of Medical Neuroscience, and Mathematics and Statistics, Dalhousie University, Halifax, Nova Scotia B3H 4R2, Canada, and Molecular Neurobiology Laboratory, the Salk Institute for Biological Studies, La Jolla, California 92037.
Christopher T Jones
Han Zhang
Jake Blacklaws
Martyn Goulding
Ying Zhang

Funding

XENOPUS NOTCH AND NEURONAL DETERMINATIONP01NS031249 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI LEMKE, GREG E · 1993 to 2011
$16.6M
Functional Analysis of Inhibitory Spinal Cord InterneuronsR37NS037075 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI GOULDING, MARTYN D · 2006 to 2012
$3.6M
CIHR MOP-110950NINDS NIH HHS P01 NS031249NINDS NIH HHS R37 NS037075
6 · The paper itself

Abstract

V3 interneurons (INs) are a major group of excitatory commissural interneurons in the spinal cord, and they are essential for producing a stable and robust locomotor rhythm. V3 INs are generated from the ventral-most progenitor domain, p3, but migrate dorsally and laterally during postmitotic development. At birth, they are located in distinctive clusters in the ventral horn and deep dorsal horn. To assess the heterogeneity of this genetically identified group of spinal INs, we combined patch-clamp recording and anatomical tracing with cluster analysis. We examined electrophysiological and morphological properties of mature V3 INs identified by their expression of tdTomato fluorescent proteins in Sim1(Cre/+); Rosa(floxstop26TdTom) mice. We identified two V3 subpopulations with distinct intrinsic properties and spatial distribution patterns. Ventral V3 INs, primarily located in lamina VIII, possess a few branching processes and were capable of generating rapid tonic firing spikes. By contrast, dorsal V3 INs exhibited a more complex morphology and relatively slow average spike frequency with strong adaptation, and they also displayed large sag voltages and post-inhibitory rebound potentials. Our data suggested that hyperpolarization-activated cation channel currents and T-type calcium channel currents may account for some of the membrane properties of V3 INs. Finally, we observed that ventral and dorsal V3 INs were active in different ways during running and swimming, indicating that ventral V3 INs may act as premotor neurons and dorsal V3 INs as relay neurons mediating sensory inputs. Together, we detected two physiologically and topographically distinct subgroups of V3 INs, each likely playing different roles in locomotor activities.

Indexed as

Action PotentialsAnimalsAnimals, NewbornBasic Helix-Loop-Helix ProteinsBenzimidazolesCardiovascular AgentsCluster AnalysisCyclopropanesElectric StimulationInterneuronsIn Vitro TechniquesMiceMice, TransgenicMotor ActivityNaphthalenesNickelBasic Helix-Loop-Helix ProteinsBenzimidazolesCardiovascular AgentsCyclopropanesGt(ROSA)26Sor non-coding RNA, mouseICI D2788NaphthalenesNickelNNC 55-0396Proto-Oncogene Proteins c-fosPyrimidinesRepressor ProteinsRNA, UntranslatedSim1 protein, mouse

Identifiers

PMID24259577
PMCPMC3894417

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.