Evidence map›Paper›PMID 22649227›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

Fgf-dependent glial cell bridges facilitate spinal cord regeneration in zebrafish.

Yona Goldshmit, Tamar E Sztal, Patricia R Jusuf, Thomas E Hall, Mai Nguyen-Chi, Peter D Currie

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 159 papers.

0numbers the graph read from it
0cells of the map it votes in
159citing papers in PubMed
11.0field-weighted citation impact, top 1% 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

159 citing papers in PubMed, 285 citations in OpenAlex.

  1. Purinergic Receptor P2Y2 Regulates Neurogenesis and Functional Recovery Following Spinal Cord Injury in Zebrafish.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Astrocytic Ryk signaling coordinates scarring and wound healing after spinal cord injury.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  17. Article
  18. Review
  19. Review
  20. A potential role of Fgf3 for epibranchial formation in zebrafish.Frontiers in cell and developmental biology · 2025
    Article

99 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 at 2 institutions in 1 country.

Yona GoldshmitAustralian Regenerative Medicine Institute, Monash University, Clayton, Victoria 3800, Australia. yona.goldshmit@med.monash.edu.au
Tamar E Sztal
Patricia R Jusuf
Thomas E Hall
Mai Nguyen-Chi
Peter D Currie
Australian Regenerative Medicine Institute · AUMonash University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adult zebrafish show a remarkable capacity to regenerate their spinal column after injury, an ability that stands in stark contrast to the limited repair that occurs within the mammalian CNS post-injury. The reasons for this interspecies difference in regenerative capacity remain unclear. Here we demonstrate a novel role for Fgf signaling during glial cell morphogenesis in promoting axonal regeneration after spinal cord injury. Zebrafish glia are induced by Fgf signaling, to form an elongated bipolar morphology that forms a bridge between the two sides of the resected spinal cord, over which regenerating axons actively migrate. Loss of Fgf function inhibits formation of this "glial bridge" and prevents axon regeneration. Despite the poor potential for mammalian axonal regeneration, primate astrocytes activated by Fgf signaling adopt a similar morphology to that induced in zebrafish glia. This suggests that differential Fgf regulation, rather than intrinsic cell differences, underlie the distinct responses of mammalian and zebrafish glia to injury.

Indexed as

Analysis of VarianceAnimalsAnimals, Genetically ModifiedBromodeoxyuridineCell DifferentiationCell MovementCell ProliferationDextransDisease Models, AnimalEnzyme InhibitorsFibroblast Growth Factor 2Fibroblast Growth Factor 3Fibroblast Growth Factor 8Gene Expression RegulationGlial Fibrillary Acidic ProteinGreen Fluorescent ProteinsBromodeoxyuridineDextransEnzyme Inhibitorsfgf3 protein, zebrafishFGF8 protein, humanFibroblast Growth Factor 2Fibroblast Growth Factor 3Fibroblast Growth Factor 8Fluoro-RubyGlial Fibrillary Acidic ProteinGreen Fluorescent ProteinsIntermediate Filament ProteinsKi-67 AntigenMitogen-Activated Protein Kinase KinasesNerve Tissue ProteinsNES protein, humanNestinPyrrolesReceptor, Fibroblast Growth Factor, Type 1RhodaminesRNA, Messengerspry4 protein, zebrafishSU 5402Zebrafish Proteins

Identifiers

PMID22649227
PMCPMC6703582
OpenAlexW2031649134

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.