Evidence map›Paper›PMID 24647935›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Selective microtubule-based transport of dendritic membrane proteins arises in concert with axon specification.

Jennifer D Petersen, Stefanie Kaech, Gary Banker

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 93 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Cellular and pathological functions of tau.Nature reviews. Molecular cell biology · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Axonal transport during injury on a theoretical axon.Frontiers in cellular neuroscience · 2023
    Article
  12. Article
  13. Article
  14. Oxidative Stress in Tauopathies: From Cause to Therapy.Antioxidants (Basel, Switzerland) · 2022
    Review
  15. Article
  16. Review
  17. Review
  18. Trafficking mechanisms underlying NaChannels (Austin, Tex.) · 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

3 authors at 2 institutions in 1 country.

Jennifer D PetersenJungers Center for Neurosciences Research, Department of Neurology, Oregon Health and Science University, Portland, Oregon 97239.
Stefanie Kaech
Gary Banker
Center for Neurosciences · USOregon Health & Science University · US

Funding

Ultrastructure and Single Particle Microscopy CoreP30NS061800 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI AICHER, SUE A · 2009 to 2020
$6.6M
Neuronal Polarity and Membrane TraffikingR01MH066179 · NIMH · RENSSELAER POLYTECHNIC INSTITUTE · PI BENTLEY, MARVIN · 2002 to 2017
$6.6M
NIMH NIH HHS MH066179NIMH NIH HHS R01 MH066179NINDS NIH HHS P30 NS061800
6 · The paper itself

Abstract

The polarized distribution of membrane proteins to axonal or somatodendritic neuronal compartments is fundamental to nearly every aspect of neuronal function. The polarity of dendritic proteins depends on selective microtubule-based transport; the vesicles that carry these proteins are transported into dendrites but do not enter the axon. We used live-cell imaging of fluorescently tagged dendritic and axonal proteins combined with immunostaining for initial segment and cytoskeletal markers to evaluate different models of dendrite-selective transport in cultured rat hippocampal neurons. In mature neurons, dendritic vesicles that entered the base of the axon stopped at the proximal edge of the axon initial segment, defined by immunostaining for ankyrinG, rather than moving into the initial segment itself. In contrast, axonal vesicles passed through the initial segment without impediment. During development, dendrite-selective transport was detected shortly after axons formed, several days before initial segment assembly, before the appearance of a dense actin meshwork in the initial segment, and before dendrites acquire microtubules of mixed polarity orientation. Indeed, some elements of selective transport were detected even before axon specification. These findings are inconsistent with models for selective transport that depend on the presence of an F-actin-based cytoplasmic filter in the initial segment or that posit that transport into dendrites is mediated by dyneins translocating along minus-end out microtubules. Instead our results suggest that selective transport involves the coordinated regulation of the different motor proteins that mediate dendritic vesicle transport and that the selectivity of motor-microtubule interactions is one facet of this process.

Indexed as

AnimalsAxonsCell PolarityHippocampusMembrane ProteinsMicrotubulesNerve Tissue ProteinsNeuronsProtein TransportRatsRats, Sprague-DawleyMembrane ProteinsNerve Tissue Proteinsaxondendritehippocampusinitial segmentmembrane trafficking

Identifiers

PMID24647935
PMCPMC3960460
OpenAlexW2004368634

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.