Evidence map›Paper›PMID 25355216›Full record

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

Maturational conversion of dendritic early endosomes and their roles in L1-mediated axon growth.

Zofia M Lasiecka, Chan Choo Yap, Joshua Katz, Bettina Winckler

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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
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  4. Dynein Is Required for Rab7-Dependent Endosome Maturation, Retrograde Dendritic Transport, and Degradation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  5. Review
  6. Review
  7. Spatial control of membrane traffic in neuronal dendrites.Molecular and cellular neurosciences · 2020
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
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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

4 authors at 1 institution in 1 country.

Zofia M LasieckaDepartment of Neuroscience, University of Virginia, Charlottesville, Virginia 22908.
Chan Choo YapDepartment of Neuroscience, University of Virginia, Charlottesville, Virginia 22908.
Joshua KatzDepartment of Neuroscience, University of Virginia, Charlottesville, Virginia 22908.
Bettina WincklerDepartment of Neuroscience, University of Virginia, Charlottesville, Virginia 22908 BWinckler@virginia.edu.ORCID http://orcid.org/0000-0002-7924-9313
University of Virginia · US

Funding

Organization and Function of Neuronal EndosomesR01NS083378 · NINDS · UNIVERSITY OF VIRGINIA · PI Bettina R Winckler · 2013 to 2026
$5.2M
NINDS NIH HHS R01 NS083378NINDS NIH HHS R01NS083378
6 · The paper itself

Abstract

The function of endosomes is intricately linked to cellular function in all cell types, including neurons. Intriguingly, neurons express cell type-specific proteins that localize to endosomes, but little is known about how these neuronal proteins interface with canonical endosomes and ubiquitously expressed endosomal components, such as EEA1 (Early Endosomal Antigen 1). NEEP21 (Neuronal Early Endosomal Protein 21 kDa) localizes to somatodendritic endosomes, and downregulation of NEEP21 perturbs the correct trafficking of multiple receptors, including glutamate receptors (GluA2) during LTP and amyloidogenic processing of βAPP. Our own work implicated NEEP21 in correct trafficking of the axonal cell adhesion molecule L1/neuron-glia cell adhesion molecule (NgCAM). NEEP21 dynamically localizes with EEA1-positive early endosomes but is also found in EEA1-negative endosomes. Live imaging reveals that NEEP21-positive, EEA1-negative endosomes arise as a consequence of maturational conversion of EEA1/NEEP21 double-positive endosomes. Interfering with EEA1 function causes missorting of L1/NgCAM, axon outgrowth defects on the L1 substrate, and disturbance of NEEP21 localization. Last, we uncover evidence that functional interference with NEEP21 reduces axon and dendrite growth of primary rat hippocampal neurons on L1 substrate but not on N-cadherin substrate, thus implicating endosomal trafficking through somatodendritic early endosomes in L1-mediated axon growth.

Indexed as

AnimalsAxonsCadherinsCells, CulturedDendritesEndocytosisEndosomesHippocampusNerve Tissue ProteinsNeural Cell Adhesion Molecule L1NeuronsRatsVesicular Transport ProteinsCadherinsearly endosome antigen 1Nerve Tissue ProteinsNeural Cell Adhesion Molecule L1Nsg1 protein, ratVesicular Transport Proteinsendosomeslive imagingNEEP21NgCAMNsg-1trafficking

Identifiers

PMID25355216
PMCPMC4212064
OpenAlexW2008163597

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.