Evidence map›Paper›PMID 17234591›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2007

Ankyrin-dependent and -independent mechanisms orchestrate axonal compartmentalization of L1 family members neurofascin and L1/neuron-glia cell adhesion molecule.

Tatiana Boiko, Max Vakulenko, Helge Ewers, Chan Choo Yap, Caren Norden, Bettina Winckler

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

66 citing papers in PubMed, 110 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. DNA Methylation in Alzheimer's Disease.Current topics in behavioral neurosciences · 2025
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Imaging of the Axon Initial Segment.Current protocols in neuroscience · 2019
    Article
  16. Article
  17. Article
  18. Axon initial segments: structure, function, and disease.Annals of the New York Academy of Sciences · 2018
    Review
  19. The Axon Initial Segment: An Updated Viewpoint.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Review
  20. The nano-architecture of the axonal cytoskeleton.Nature reviews. Neuroscience · 2017
    Review

6 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

6 authors at 4 institutions in 1 country.

Tatiana BoikoDepartment of Neuroscience, University of Virginia, Charlottesville, Virginia 22908, USA.
Max Vakulenko
Helge Ewers
Chan Choo Yap
Caren Norden
Bettina Winckler
University of Virginia · USMaine School of Science and Mathematics · USUConn Health · USYale University · US

Funding

Targeting Pathways of Axonal Cell Adhesion MoleculesR01NS045969 · NINDS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI WINCKLER, BETTINA R · 2003 to 2007
$1.5M
NINDS NIH HHS 1R01NS 045969-01NINDS NIH HHS R01 NS045969
6 · The paper itself

Abstract

Axonal initial segments (IS) and nodes of Ranvier are functionally important membrane subdomains in which the clustering of electrogenic channels enables action potential initiation and propagation. In addition, the initial segment contributes to neuronal polarity by serving as a diffusion barrier. To study the mechanisms of axonal compartmentalization, we focused on two L1 family of cell adhesion molecules (L1-CAMs) [L1/neuron-glia cell adhesion molecule (L1/NgCAM) and neurofascin (NF)] and two neuronal ankyrins (ankB and ankG). NF and ankG accumulate specifically at the initial segment, whereas L1/NgCAM and ankB are expressed along the entire lengths of axons. We find that L1/NgCAM and NF show distinct modes of steady-state accumulation during axon outgrowth in cultured hippocampal neurons. Despite their different steady-state localizations, both L1/NgCAM and NF show slow diffusion and low detergent extractability specifically in the initial segment but fast diffusion and high detergent extractability in the distal axon. We propose that L1-CAMs do not strongly bind ankB in the distal axon because of spatial regulation of ankyrin affinity by phosphorylation. NF, conversely, is initially enriched in an ankyrin-independent manner in the axon generally and accumulates progressively in the initial segment attributable to preferential binding to ankG. Our results suggest that NF and L1/NgCAM accumulate in the axon by an ankyrin-independent pathway, but retention at the IS requires ankyrin binding.

Indexed as

Multigene FamilyAnimalsAnkyrinsAxonsCell Adhesion MoleculesCell Adhesion Molecules, Neuron-GliaCell LineCells, CulturedHumansNerve Growth FactorsNeural Cell Adhesion Molecule L1NeuronsProtein BindingRatsAnkyrinsCell Adhesion MoleculesCell Adhesion Molecules, Neuron-GliaNerve Growth FactorsNeural Cell Adhesion Molecule L1Nfasc protein, rat

Identifiers

PMID17234591
PMCPMC6672792
OpenAlexW1985234764

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.