Evidence map›Paper›PMID 22681863›Full record

ArticleNeural development2012

Dynamics of degeneration and regeneration in developing zebrafish peripheral axons reveals a requirement for extrinsic cell types.

Rosario Villegas, Seanna M Martin, Kelley C O'Donnell, Simon A Carrillo, Alvaro Sagasti, Miguel L Allende

Open access · goldAbstract read
In one paragraph

Article in Neural development, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

40 citing papers in PubMed, 88 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Hair Cell Regeneration: From Animals to Humans.Clinical and experimental otorhinolaryngology · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Current neuropharmacology · 2022
    Review
  14. Lessons from Injury: How Nerve Injury Studies Reveal Basic Biological Mechanisms and Therapeutic Opportunities for Peripheral Nerve Diseases.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2021
    Review
  15. Article
  16. Review
  17. Article
  18. Role of Macrophages and Microglia in Zebrafish Regeneration.International journal of molecular sciences · 2020
    Review
  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

6 authors at 2 institutions in 2 countries.

Rosario VillegasFONDAP Center for Genome Regulation, Facultad de Ciencias, Universidad de Chile, Las Palmeras 3425, Santiago, Chile.
Seanna M Martin
Kelley C O'Donnell
Simon A Carrillo
Alvaro Sagasti
Miguel L Allende
University of California, Los Angeles · USUniversity of Chile · CL

Funding

UCLA-Caltech Medical Scientist Training ProgramT32GM008042 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AJIJOLA, OLUJIMI A, DAWSON, DAVID WAYNE · 1985 to 2023
$29.9M
TRAINING PROGRAM IN NEURAL REPAIRT32NS007449 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHESSELET, MARIE-FRANCOISE S · 1998 to 2012
$1.9M
NIGMS NIH HHS T32 GM008042NINDS NIH HHS 5/T32/NS07449:13
6 · The paper itself

Abstract

backgroundUnderstanding the cellular mechanisms regulating axon degeneration and regeneration is crucial for developing treatments for nerve injury and neurodegenerative disease. In neurons, axon degeneration is distinct from cell body death and often precedes or is associated with the onset of disease symptoms. In the peripheral nervous system of both vertebrates and invertebrates, after degeneration of detached fragments, axons can often regenerate to restore function. Many studies of axonal degeneration and regeneration have used in vitro approaches, but the influence of extrinsic cell types on these processes can only be fully addressed in live animals. Because of its simplicity and superficial location, the larval zebrafish posterior lateral line (pLL) nerve is an ideal model system for live studies of axon degeneration and regeneration.

resultsWe used laser axotomy and time-lapse imaging of pLL axons to characterize the roles of leukocytes, Schwann cells and target sensory hair cells in axon degeneration and regeneration in vivo. Immune cells were essential for efficient removal of axonal debris after axotomy. Schwann cells were required for proper fasciculation and pathfinding of regenerating axons to their target cells. Intact target hair cells were not themselves required for regeneration, but chemical ablation of neuromasts caused axons to transiently deviate from their normal paths.

conclusionsMacrophages, Schwann cells, and target sensory organs are required for distinct aspects of pLL axon degeneration or regeneration in the zebrafish larva. Our work introduces a powerful vertebrate model for analyzing axonal degeneration and regeneration in the living animal and elucidating the role of extrinsic cell types in these processes.

Indexed as

Analysis of VarianceAnimalsAnimals, Genetically ModifiedAxonsAxotomyCopperEmbryo, NonmammalianEnzyme InhibitorsGene Expression Regulation, DevelopmentalGreen Fluorescent ProteinsMutationNerve DegenerationNerve RegenerationNeuronsOligodeoxyribonucleotides, AntisensePeripheral NervesAtoh1a protein, zebrafishCopperEnzyme InhibitorsGreen Fluorescent ProteinsOligodeoxyribonucleotides, AntisenseProto-Oncogene ProteinsProto-Oncogene Protein Spi-1QuinazolinesRTKI cpdTrans-ActivatorsTranscription FactorsTyrphostinsZebrafish Proteins

Identifiers

PMID22681863
PMCPMC3780720
OpenAlexW2130059100

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.