Evidence map›Paper›PMID 20943924›Full record

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

Analysis of the astray/robo2 zebrafish mutant reveals that degenerating tracts do not provide strong guidance cues for regenerating optic axons.

Cameron Wyatt, Anselm Ebert, Michell M Reimer, Kendall Rasband, Melissa Hardy, Chi-Bin Chien, Thomas Becker, Catherina G Becker

Open access · bronzeAbstract read
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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Serotonin neuromodulation directs optic nerve regeneration.Development (Cambridge, England) · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Regeneration of Dopaminergic Neurons in Adult Zebrafish Depends on Immune System Activation and Differs for Distinct Populations.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Robo2--slit and Dcc--netrin1 coordinate neuron axonal pathfinding within the embryonic axon tracts.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    Article
  14. In vivo nerve-macrophage interactions following peripheral nerve injury.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    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 2 institutions in 2 countries.

Cameron WyattCentre for Neuroregeneration, School of Biomedical Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Anselm Ebert
Michell M Reimer
Kendall Rasband
Melissa Hardy
Chi-Bin Chien
Thomas Becker
Catherina G Becker
University of Edinburgh · GBUniversity of Utah · US

Funding

University of Utah, Core Vision Research GrantP30EY014800 · NEI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI PAUL STEVEN BERNSTEIN · 2005 to 2026
$14.6M
RETINAL AXON PATHFINDING MUTANTS IN ZEBRAFISHR01EY012873 · NEI · UNIVERSITY OF UTAH · PI VETTER, MONICA L · 2000 to 2011
$4.0M
Biotechnology and Biological Sciences Research CouncilNEI NIH HHS P30 EY014800NEI NIH HHS R01 EY012873NEI NIH HHS R01 EY12873Wellcome TrustWellcome Trust WT078052
6 · The paper itself

Abstract

During formation of the optic projection in astray/robo2 mutant zebrafish, optic axons exhibit rostrocaudal pathfinding errors, ectopic midline crossing and increased terminal arbor size. Here we show that these errors persist into adulthood, even when robo2 function is conditionally reduced only during initial formation of the optic projection. Adult errors include massive ectopic optic tracts in the telencephalon. During optic nerve regeneration in astray/robo2 animals, these tracts are not repopulated and ectopic midline crossing is reduced compared with unlesioned mutants. This is despite a comparable macrophage/microglial response and upregulation of contactin1a in oligodendrocytes of entopic and ectopic tracts. However, other errors, such as expanded termination areas and ectopic growth into the tectum, were frequently recommitted by regenerating optic axons. Retinal ganglion cells with regenerating axons reexpress robo2 and expression of slit ligands is maintained in some areas of the adult optic pathway. However, slit expression is reduced rostral and caudal to the chiasm, compared with development and ubiquitous overexpression of Slit2 did not elicit major pathfinding phenotypes. This shows that (1) there is not an efficient correction mechanism for large-scale pathfinding errors of optic axons during development; (2) degenerating tracts do not provide a strong guidance cue for regenerating optic axons in the adult CNS, unlike the PNS; and (3) robo2 is less important for pathfinding of optic axons during regeneration than during development.

Indexed as

AnimalsAxonsImmunohistochemistryIn Situ HybridizationNerve DegenerationNerve RegenerationOptic NerveReceptors, ImmunologicRoundabout ProteinsZebrafishZebrafish ProteinsReceptors, Immunologicrobo2 protein, zebrafishRoundabout ProteinsZebrafish Proteins

Identifiers

PMID20943924
PMCPMC3058139
OpenAlexW2025616602

What OpenQuestion holds

Textmetadata
LicenceTDM
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.