Evidence map›Paper›PMID 26161965›Full record

ArticlePloS one2015

Co-Orientation: Quantifying Simultaneous Co-Localization and Orientational Alignment of Filaments in Light Microscopy.

Robert P J Nieuwenhuizen, Leila Nahidiazar, Erik M M Manders, Kees Jalink, Sjoerd Stallinga, Bernd Rieger

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
6.2field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Intercellular Communication Through Microtubular Highways.Results and problems in cell differentiation · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Kinesin-dependent transport of keratin filaments: a unified mechanism for intermediate filament transport.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. 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

6 authors at 3 institutions in 1 country.

Robert P J NieuwenhuizenQuantitative Imaging group, Department of Imaging Physics, Delft University of Technology, Delft, The Netherlands.
Leila NahidiazarCell Biophysics group, Department of Cell biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Erik M M MandersVan Leeuwenhoek Centre for Advanced Microscopy, Molecular Cytology, Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, The Netherlands.
Kees JalinkCell Biophysics group, Department of Cell biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Sjoerd StallingaQuantitative Imaging group, Department of Imaging Physics, Delft University of Technology, Delft, The Netherlands.
Bernd RiegerQuantitative Imaging group, Department of Imaging Physics, Delft University of Technology, Delft, The Netherlands.
Delft University of Technology · NLThe Netherlands Cancer Institute · NLUniversity of Amsterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Co-localization analysis is a widely used tool to seek evidence for functional interactions between molecules in different color channels in microscopic images. Here we extend the basic co-localization analysis by including the orientations of the structures on which the molecules reside. We refer to the combination of co-localization of molecules and orientational alignment of the structures on which they reside as co-orientation. Because the orientation varies with the length scale at which it is evaluated, we consider this scale as a separate informative dimension in the analysis. Additionally we introduce a data driven method for testing the statistical significance of the co-orientation and provide a method for visualizing the local co-orientation strength in images. We demonstrate our methods on simulated localization microscopy data of filamentous structures, as well as experimental images of similar structures acquired with localization microscopy in different color channels. We also show that in cultured primary HUVEC endothelial cells, filaments of the intermediate filament vimentin run close to and parallel with microtubuli. In contrast, no co-orientation was found between keratin and actin filaments. Co-orientation between vimentin and tubulin was also observed in an endothelial cell line, albeit to a lesser extent, but not in 3T3 fibroblasts. These data therefore suggest that microtubuli functionally interact with the vimentin network in a cell-type specific manner.

Indexed as

3T3 CellsAlgorithmsAnimalsCell LineCells, CulturedComputational BiologyComputer SimulationFibroblastsHumansHuman Umbilical Vein Endothelial CellsIntermediate FilamentsMiceMicroscopy, FluorescenceModels, BiologicalProtein BindingTubulinTubulinVimentin

Identifiers

PMID26161965
PMCPMC4498647
OpenAlexW1862553826

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.