Evidence map›Paper›PMID 18524906›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2008

Axonal injury and regeneration in the adult brain of Drosophila.

Derya Ayaz, Maarten Leyssen, Marta Koch, Jiekun Yan, Mohammed Srahna, Vasu Sheeba, Keri J Fogle, Todd C Holmes, Bassem A Hassan

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

61 citing papers in PubMed, 108 citations in OpenAlex.

  1. Article
  2. The Repair Manual of a Fruit Fly Brain.International journal of molecular sciences · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. TBI and Tau Loss of Function Both Affect Naïve Ethanol Sensitivity inInternational journal of molecular sciences · 2024
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Drosophila as a model to explore secondary injury cascades after traumatic brain injury.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2021
    Review
  13. A molecular toolkit for superorganisms.Trends in genetics : TIG · 2021
    Review
  14. Article
  15. Modeling Neurodegenerative Disorders inInternational journal of molecular sciences · 2020
    Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

1 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

9 authors at 2 institutions in 3 countries.

Derya AyazLaboratory of Neurogenetics, Department of Molecular and Developmental Genetics, Flanders Institute for Biotechnology (VIB), 3000 Leuven, Belgium.
Maarten Leyssen
Marta Koch
Jiekun Yan
Mohammed Srahna
Vasu Sheeba
Keri J Fogle
Todd C Holmes
Bassem A Hassan
Vlaams Instituut voor Biotechnologie · BEUniversity of California, Irvine · US

Funding

Electrical Signaling in a Circadian Pacemaker CircuitR01NS046750 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI HOLMES, TODD C · 2004 to 2013
$2.4M
NINDS NIH HHS R01 NS046750NINDS NIH HHS R01-NS046750
6 · The paper itself

Abstract

Drosophila melanogaster is a leading genetic model system in nervous system development and disease research. Using the power of fly genetics in traumatic axonal injury research will significantly speed up the characterization of molecular processes that control axonal regeneration in the CNS. We developed a versatile and physiologically robust preparation for the long-term culture of the whole Drosophila brain. We use this method to develop a novel Drosophila model for CNS axonal injury and regeneration. We first show that, similar to mammalian CNS axons, injured adult wild-type fly CNS axons fail to regenerate, whereas adult-specific enhancement of protein kinase A activity increases the regenerative capacity of lesioned neurons. Combined, these observations suggest conservation of neuronal regeneration mechanisms after injury. We next exploit this model to explore pathways that induce robust regeneration and find that adult-specific activation of c-Jun N-terminal protein kinase signaling is sufficient for de novo CNS axonal regeneration injury, including the growth of new axons past the lesion site and into the normal target area.

Indexed as

Age FactorsAnimalsAxonsBrainCells, CulturedDiffuse Axonal InjuryDisease Models, AnimalDrosophila melanogasterNerve RegenerationOrgan Culture Techniques

Identifiers

PMID18524906
PMCPMC2693324
OpenAlexW1987798862

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.