Evidence map›Paper›PMID 28389579›Full record

ArticleJournal of cell science2017

Microtubule organization within mitotic spindles revealed by serial block face scanning electron microscopy and image analysis.

Faye M Nixon, Thomas R Honnor, Nicholas I Clarke, Georgina P Starling, Alison J Beckett, Adam M Johansen, Julia A Brettschneider, Ian A Prior, Stephen J Royle

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed, 50 citations in OpenAlex.

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  12. Anaphase B: Long-standing models meet new concepts.Seminars in cell & developmental biology · 2021
    Review
  13. Review
  14. Article
  15. Moonlighting of mitotic regulators in cilium disassembly.Cellular and molecular life sciences : CMLS · 2021
    Review
  16. Article
  17. Mitotic spindle: lessons from theoretical modeling.Molecular biology of the cell · 2021
    Article
  18. Article
  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

9 authors at 2 institutions in 1 country.

Faye M NixonCentre for Mechanochemical Cell Biology, Warwick Medical School, Coventry CV4 7AL, UK.ORCID 0000-0002-7029-2649
Thomas R HonnorDepartment of Statistics, University of Warwick, Coventry CV4 7AL, UK.
Nicholas I ClarkeCentre for Mechanochemical Cell Biology, Warwick Medical School, Coventry CV4 7AL, UK.
Georgina P StarlingCentre for Mechanochemical Cell Biology, Warwick Medical School, Coventry CV4 7AL, UK.
Alison J BeckettInstitute for Translational Medicine, University of Liverpool L69 3BX, UK.
Adam M JohansenDepartment of Statistics, University of Warwick, Coventry CV4 7AL, UK.
Julia A BrettschneiderDepartment of Statistics, University of Warwick, Coventry CV4 7AL, UK.
Ian A PriorInstitute for Translational Medicine, University of Liverpool L69 3BX, UK.ORCID 0000-0002-4055-5161
Stephen J RoyleCentre for Mechanochemical Cell Biology, Warwick Medical School, Coventry CV4 7AL, UK s.j.royle@warwick.ac.uk.ORCID 0000-0001-8927-6967
University of Liverpool · GBUniversity of Warwick · GB

Funding

Cancer Research UK 15182Cancer Research UK C25425/A15182
6 · The paper itself

Abstract

Serial block face scanning electron microscopy (SBF-SEM) is a powerful method to analyze cells in 3D. Here, working at the resolution limit of the method, we describe a correlative light-SBF-SEM workflow to resolve microtubules of the mitotic spindle in human cells. We present four examples of uses for this workflow that are not practical by light microscopy and/or transmission electron microscopy. First, distinguishing closely associated microtubules within K-fibers; second, resolving bridging fibers in the mitotic spindle; third, visualizing membranes in mitotic cells, relative to the spindle apparatus; and fourth, volumetric analysis of kinetochores. Our workflow also includes new computational tools for exploring the spatial arrangement of microtubules within the mitotic spindle. We use these tools to show that microtubule order in mitotic spindles is sensitive to the level of TACC3 on the spindle.

Indexed as

Image Processing, Computer-AssistedHeLa CellsHumansImaging, Three-DimensionalKinetochoresMicroscopy, Electron, ScanningMicrotubulesModels, BiologicalModels, MolecularSpindle Apparatus3D cell biologyElectron microscopyMicrotubulesMitosisMitotic spindleStatistics

Identifiers

PMID28389579
PMCPMC6173286
OpenAlexW2951645735

What OpenQuestion holds

Textmetadata
LicenceTDM
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.