Evidence map›Paper›PMID 8601604›Full record

ArticleThe Journal of cell biology1996

Microtubule transport and assembly during axon growth.

W Yu, M J Schwei, P W Baas

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Review
  3. Stability properties of neuronal microtubules.Cytoskeleton (Hoboken, N.J.) · 2016
    Review
  4. Article
  5. Signaling Over Distances.Molecular & cellular proteomics : MCP · 2016
    Review
  6. Review
  7. The enhancement effect of beta-boswellic acid on hippocampal neurites outgrowth and branching (an in vitro study).Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2010
    Article
  8. Loss of neurofilaments alters axonal growth dynamics.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2001
    Article
  9. Article
  10. Neurofilaments are transported rapidly but intermittently in axons: implications for slow axonal transport.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2000
    Article
  11. Article
  12. Reorganization and movement of microtubules in axonal growth cones and developing interstitial branches.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1999
    Article
  13. Different contributions of microtubule dynamics and transport to the growth of axons and collateral sprouts.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1999
    Article
  14. Article
  15. Article
  16. Microtubule transport from the cell body into the axons of growing neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1997
    Article
  17. Article
  18. Functional analysis of dynactin and cytoplasmic dynein in slow axonal transport.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1996
    Article
  19. Microtubule assembly in growing dendrites.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1996
    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

3 authors at 1 institution in 1 country.

W YuDepartment of Anatomy, University of Wisconsin Medical School, Madison, 53706, USA.
M J Schwei
P W Baas
University of Wisconsin System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is controversy concerning the mechanisms by which the axonal microtubule (MT) array is elaborated, with some models focusing on MT assembly and other models focusing on MT transport. We have proposed a composite model in which MT assembly and transport are both important (Joshi, H.C., and P.W. Baas. 1993. J. Cell Biol. 121:1191-1196). In the present study, we have taken a novel approach to evaluate the merits of this proposal. Biotinylated tubulin was microinjected into cultured neurons that had already grown short axons. The axons were then permitted to grow longer, after which the cells were prepared for immunoelectron microscopic analyses. We reasoned that any polymer that assembled or turned over subunits after the introduction of the probe should label for biotin, while any polymer that was already assembled but did not turnover should not label. Therefore, the presence in the newly grown region of the axon of any unlabeled MT polymer is indicative of MT transport. In sampled regions, the majority of the polymer was labeled, indicating that MT assembly events are active during axon growth. Varying amounts of unlabeled polymer were also present in the newly grown regions, indicating that MT transport also occurs. Together these findings demonstrate that MT assembly and transport both contribute to the elaboration of the axonal MT array.

Indexed as

AnimalsAxonsBiological TransportBiotinCells, CulturedMicroinjectionsMicroscopy, Phase-ContrastMicrotubulesRatsSympathetic Nervous SystemBiotin

Identifiers

PMID8601604
PMCPMC2120775
OpenAlexW2065498871

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.