Evidence map›Paper›PMID 10516309›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1999

Reorganization and movement of microtubules in axonal growth cones and developing interstitial branches.

E W Dent, J L Callaway, G Szebenyi, P W Baas, K Kalil

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers.

0numbers the graph read from it
0cells of the map it votes in
109citing 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

109 citing papers in PubMed.

  1. Article
  2. Fidgetin binds spastin to attenuate the microtubule-severing activity.Biochimica et biophysica acta. Molecular cell research · 2025
    Article
  3. Review
  4. Article
  5. Molecular cartography within axons.Current opinion in cell biology · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. The Role of Spastin in Axon Biology.Frontiers in cell and developmental biology · 2022
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

49 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

5 authors.

E W DentNeuroscience Training Program, University of Wisconsin, Madison, Wisconsin 53706, USA.
J L Callaway
G Szebenyi
P W Baas
K Kalil

Funding

NEUROSCIENCE TRAINING PROGRAMT32GM007507 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI HALLORAN, MARY C · 1985 to 2017
$9.3M
DEVELOPMENTAL STUDIES ON THE MOTOR SYSTEMR01NS014428 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI KALIL, KATHERINE · 1985 to 2015
$3.6M
DYNAMICS OF THE NEURONAL CYTOSKELETONR01NS034270 · NINDS · UNIVERSITY OF WISCONSIN MADISON · PI BAAS, PETER W · 1996 to 2003
$1.4M
Developmental Studies on the Motor SystemR56NS014428 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI KALIL, KATHERINE · 2010 to 2010
$361k
NIGMS NIH HHS GM07507NIGMS NIH HHS T32 GM007507NINDS NIH HHS NS 14428NINDS NIH HHS NS 34270NINDS NIH HHS R01 NS014428NINDS NIH HHS R01 NS034270NINDS NIH HHS R56 NS014428
6 · The paper itself

Abstract

Local changes in microtubule organization and distribution are required for the axon to grow and navigate appropriately; however, little is known about how microtubules (MTs) reorganize during directed axon outgrowth. We have used time-lapse digital imaging of developing cortical neurons microinjected with fluorescently labeled tubulin to follow the movements of individual MTs in two regions of the axon where directed growth occurs: the terminal growth cone and the developing interstitial branch. In both regions, transitions from quiescent to growth states were accompanied by reorganization of MTs from looped or bundled arrays to dispersed arrays and fragmentation of long MTs into short MTs. We also found that long-term redistribution of MTs accompanied the withdrawal of some axonal processes and the growth and stabilization of others. Individual MTs moved independently in both anterograde and retrograde directions to explore developing processes. Their velocities were inversely proportional to their lengths. Our results demonstrate directly that MTs move within axonal growth cones and developing interstitial branches. Our findings also provide the first direct evidence that similar reorganization and movement of individual MTs occur in the two regions of the axon where directed outgrowth occurs. These results suggest a model whereby short exploratory MTs could direct axonal growth cones and interstitial branches toward appropriate locations.

Indexed as

AnimalsAxonsCattleCells, CulturedCerebral CortexGrowth ConesMicroscopy, FluorescenceMicrotubulesNeuronal PlasticityNeurons

Identifiers

PMID10516309
PMCPMC6782770

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.