Evidence map›Paper›PMID 12040061›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2002

Slit2, a branching-arborization factor for sensory axons in the Mammalian CNS.

P Hande Ozdinler, Reha S Erzurumlu

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

34 citing papers in PubMed, 90 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. The Role of Neurodevelopmental Pathways in Brain Tumors.Frontiers in cell and developmental biology · 2021
    Review
  7. Article
  8. Article
  9. Development of tactile sensory circuits in the CNS.Current opinion in neurobiology · 2018
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. A sympathetic neuron autonomous role for Egr3-mediated gene regulation in dendrite morphogenesis and target tissue innervation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  17. Molecular control of axon branching.The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry · 2013
    Review
  18. Article
  19. Article
  20. Review
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

2 authors at 1 institution in 1 country.

P Hande OzdinlerDepartment of Cell Biology and Anatomy, Louisiana State University Health Sciences Center, New Orleans, Louisiana 70112, USA.
Reha S Erzurumlu
Louisiana State University Health Sciences Center New Orleans · US

Funding

Thalamocortical Boundary Markers and the Influence of SerotoninP01NS049048 · NINDS · WASHINGTON UNIVERSITY · PI JACQUIN, MARK F · 2006 to 2010
$5.8M
NINDS NIH HHS P01 NS049048
6 · The paper itself

Abstract

Axons that carry information from the sensory periphery first elongate unbranched and form precisely ordered tracts within the CNS. Later, they begin collateralizing into their proper targets and form terminal arbors. Target-derived factors that govern sensory axon elongation and branching-arborization are not well understood. Here we report that Slit2 is a major player in branching-arborization of central trigeminal axons in the brainstem. Embryonic trigeminal axons initially develop unbranched as they form the trigeminal tract within the lateral brainstem; later, they emit collateral branches into the brainstem trigeminal nuclei and form terminal arbors therein. In whole-mount explant cultures of this pathway, embryonic day 15 (E15) rat central trigeminal axons retain their unbranched growth within the tract, whereas E17 trigeminal axons show branching and arborization in the brainstem trigeminal nuclei, much like that seen in vivo. Similar observations were made in E13 and E15 mouse embryos. We cocultured Slit2-expressing tissues or cells with the whole-mount explant cultures of the central trigeminal pathway derived from embryonic rats or mice. When central trigeminal axons are exposed to ectopic Slit2 during their elongation phase, they show robust and premature branching and arborization. Blocking available Slit2 reverses this effect on axon growth. Spatiotemporal expression of Slit2 and Robo receptor mRNAs within the brainstem trigeminal nuclei and the trigeminal ganglion during elongation and branching-arborization further corroborates our experimental results.

Indexed as

AnimalsAxonsBrain StemCells, CulturedChoroid PlexusCoculture TechniquesGene Expression Regulation, DevelopmentalHumansIntercellular Signaling Peptides and ProteinsKidneyMiceNerve Tissue ProteinsNeurons, AfferentRatsReceptors, ImmunologicRNA, MessengerIntercellular Signaling Peptides and ProteinsNerve Tissue ProteinsReceptors, ImmunologicRNA, MessengerRoundabout ProteinsSlit Homolog 2 Protein

Identifiers

PMID12040061
PMCPMC4260804
OpenAlexW2152236543

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.