Evidence map›Paper›PMID 12122060›Full record

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

Microtubule reconfiguration during axonal retraction induced by nitric oxide.

Yan He, Wenqian Yu, Peter W Baas

Abstract 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 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
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

28 citing papers in PubMed.

  1. Article
  2. eLife · 2022
    Article
  3. Article
  4. Article
  5. FOXO Regulates Neuromuscular Junction Homeostasis DuringFrontiers in aging neuroscience · 2020
    Article
  6. Article
  7. Article
  8. Mitotic Motor KIFC1 Is an Organizer of Microtubules in the Axon.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  9. Article
  10. Article
  11. Article
  12. Different modes of growth cone collapse in NG 108-15 cells.European biophysics journal : EBJ · 2013
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. NMDA receptor activation suppresses microtubule growth and spine entry.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  18. Nitric oxide synthase regulates morphogenesis of zebrafish spinal cord motoneurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2010
    Article
  19. Article
  20. 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

3 authors.

Yan HeDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, Pennsylvania 19129, USA.
Wenqian Yu
Peter W Baas

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Axonal retraction is induced by different types of physiological cues and is responsible for the elimination of mistargeted axons. There is broad agreement that alterations in the cytoskeleton underlie axonal retraction. The prevailing view is that axonal retraction involves a wholesale depolymerization of microtubules and microfilaments. However, axons retracting physiologically display a very different morphology than axons induced to retract by experimental depolymerization of microtubules. Experimental depolymerization of microfilaments actually prevents retraction rather than causing it. We have proposed an alternative hypothesis, namely that axonal retraction involves a backward retreat of cytoskeletal elements rather than their wholesale depolymerization. In the present study, we sought to test this hypothesis with regard to microtubules. When a donor of nitric oxide was applied to cultured chick sensory neurons, the majority of axons retracted dramatically within 30-60 min. Retracting axons were characterized by an enlarged distal region, a thin trailing remnant, and sinusoidal bends along the shaft. Quantitative immunofluorescence analyses showed no detectable loss of microtubule mass during retraction, even with regard to the most labile microtubules. Instead, microtubules were reconfigured into coiling and sinusoidal bundles to accommodate the shortening of the axon. Stabilization of microtubules by taxol did not prevent the retraction, even at concentrations of the drug that actually caused microtubule levels to increase. The retractions induced by nitric oxide were remarkably similar to those observed when motor proteins are manipulated, suggesting that these retractions may result from alterations in the activities of the motors that configure microtubules.

Indexed as

AnimalsAntineoplastic AgentsAxonsCells, CulturedChick EmbryoCytoskeletonGanglia, SpinalHydrazinesMicroscopy, FluorescenceMicrotubulesNeuronsNitric OxideNitric Oxide DonorsNocodazolePaclitaxelTubulin3-(2-hydroxy-1-methyl-2-nitrosohydrazino)-N-methyl-1-propanamineAntineoplastic AgentsHydrazinesNitric OxideNitric Oxide DonorsNocodazolePaclitaxelTubulinTyrosine

Identifiers

PMID12122060
PMCPMC6757941

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.