Evidence map›Paper›PMID 28205572›Full record

ArticleScientific reports2017

Ran-dependent TPX2 activation promotes acentrosomal microtubule nucleation in neurons.

Wen-Shin Chen, Yi-Ju Chen, Yung-An Huang, Bing-Yuan Hsieh, Ho-Chieh Chiu, Pei-Ying Kao, Chih-Yuan Chao, Eric Hwang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

21 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Building on-chip cytoskeletal circuits via branched microtubule networks.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Article
  9. How Microtubules Build the Spindle Branch by Branch.Annual review of cell and developmental biology · 2022
    Review
  10. An in vitro model of neuronal ensembles.Nature communications · 2022
    Article
  11. Article
  12. Review
  13. Article
  14. Dynamic microtubules at the synapse.Current opinion in neurobiology · 2020
    Review
  15. Article
  16. Review
  17. Microtubule control of functional architecture in neurons.Current opinion in neurobiology · 2019
    Review
  18. Article
  19. PAR3-PAR6-atypical PKC polarity complex proteins in neuronal polarization.Cellular and molecular life sciences : CMLS · 2018
    Review
  20. Article
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

8 authors at 1 institution in 1 country.

Wen-Shin ChenDepartment of Biological Science and Technology, National Chiao Tung University, Hsinchu, Taiwan.
Yi-Ju ChenInstitute of Molecular Medicine and Bioengineering, National Chiao Tung University, Hsinchu, Taiwan.
Yung-An HuangDepartment of Biological Science and Technology, National Chiao Tung University, Hsinchu, Taiwan.
Bing-Yuan HsiehInstitute of Molecular Medicine and Bioengineering, National Chiao Tung University, Hsinchu, Taiwan.
Ho-Chieh ChiuInstitute of Molecular Medicine and Bioengineering, National Chiao Tung University, Hsinchu, Taiwan.
Pei-Ying KaoInstitute of Bioinformatics and Systems Biology, National Chiao Tung University, Hsinchu, Taiwan.
Chih-Yuan ChaoInstitute of Molecular Medicine and Bioengineering, National Chiao Tung University, Hsinchu, Taiwan.
Eric HwangDepartment of Biological Science and Technology, National Chiao Tung University, Hsinchu, Taiwan.
National Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The microtubule (MT) cytoskeleton is essential for the formation of morphologically appropriate neurons. The existence of the acentrosomal MT organizing center in neurons has been proposed but its identity remained elusive. Here we provide evidence showing that TPX2 is an important component of this acentrosomal MT organizing center. First, neurite elongation is compromised in TPX2-depleted neurons. In addition, TPX2 localizes to the centrosome and along the neurite shaft bound to MTs. Depleting TPX2 decreases MT formation frequency specifically at the tip and the base of the neurite, and these correlate precisely with the regions where active GTP-bound Ran proteins are enriched. Furthermore, overexpressing the downstream effector of Ran, importin, compromises MT formation and neuronal morphogenesis. Finally, applying a Ran-importin signaling interfering compound phenocopies the effect of TPX2 depletion on MT dynamics. Together, these data suggest a model in which Ran-dependent TPX2 activation promotes acentrosomal MT nucleation in neurons.

Indexed as

alpha KaryopherinsAnimalsbeta KaryopherinsCell Cycle ProteinsCentrosomeGuanosine TriphosphateHippocampusMice, Inbred C57BLMicrotubule-Associated ProteinsMicrotubulesModels, BiologicalMorphogenesisNeuritesNeuronsNuclear ProteinsProtein Bindingalpha Karyopherinsbeta KaryopherinsCell Cycle ProteinsGuanosine TriphosphateimportazoleMicrotubule-Associated ProteinsNuclear ProteinsQuinazolinesran GTP-Binding ProteinTPX2 protein, mouse

Identifiers

PMID28205572
PMCPMC5304320
OpenAlexW2589113976

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.