Evidence map›Paper›PMID 25313407›Full record

ArticleThe Journal of cell biology2014

Isotropic actomyosin dynamics promote organization of the apical cell cortex in epithelial cells.

Christoph Klingner, Anoop V Cherian, Johannes Fels, Philipp M Diesinger, Roland Aufschnaiter, Nicola Maghelli, Thomas Keil, Gisela Beck, Iva M Tolić-Nørrelykke, Mark Bathe and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact, top 96% 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

18 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Plasticity of the brush border - the yin and yang of intestinal homeostasis.Nature reviews. Gastroenterology & hepatology · 2016
    Review
  16. Article
  17. Article
  18. Move your microvilli.The Journal of cell biology · 2014
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 4 countries.

Christoph KlingnerCellular Dynamics and Cell Patterning and Department of Molecular Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany Institute of Cell Dynamics and Imaging and Cells-In-Motion Cluster of Excellence (EXC1003-CiM), University of Münster, 48149 Münster, Germany Institute of Cell Dynamics and Imaging and Cells-In-Motion Cluster of Excellence (EXC1003-CiM), University of Münster, 48149 Münster, Germany.
Anoop V CherianCellular Dynamics and Cell Patterning and Department of Molecular Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.
Johannes FelsInstitute of Cell Dynamics and Imaging and Cells-In-Motion Cluster of Excellence (EXC1003-CiM), University of Münster, 48149 Münster, Germany Institute of Cell Dynamics and Imaging and Cells-In-Motion Cluster of Excellence (EXC1003-CiM), University of Münster, 48149 Münster, Germany.
Philipp M DiesingerLaboratory for Computational Biology & Biophysics, Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.
Roland AufschnaiterCellular Dynamics and Cell Patterning and Department of Molecular Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany Institute of Cell Dynamics and Imaging and Cells-In-Motion Cluster of Excellence (EXC1003-CiM), University of Münster, 48149 Münster, Germany Institute of Cell Dynamics and Imaging and Cells-In-Motion Cluster of Excellence (EXC1003-CiM), University of Münster, 48149 Münster, Germany.
Nicola MaghelliMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.
Thomas KeilCellular Dynamics and Cell Patterning and Department of Molecular Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.
Gisela BeckCellular Dynamics and Cell Patterning and Department of Molecular Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany Institute of Cell Dynamics and Imaging and Cells-In-Motion Cluster of Excellence (EXC1003-CiM), University of Münster, 48149 Münster, Germany Institute of Cell Dynamics and Imaging and Cells-In-Motion Cluster of Excellence (EXC1003-CiM), University of Münster, 48149 Münster, Germany.
Iva M Tolić-NørrelykkeMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany Division of Molecular Biology, Ruđer Bošković Institute, 10000 Zagreb, Croatia.
Mark BatheLaboratory for Computational Biology & Biophysics, Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.
Roland Wedlich-SoldnerCellular Dynamics and Cell Patterning and Department of Molecular Structural Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany Institute of Cell Dynamics and Imaging and Cells-In-Motion Cluster of Excellence (EXC1003-CiM), University of Münster, 48149 Münster, Germany Institute of Cell Dynamics and Imaging and Cells-In-Motion Cluster of Excellence (EXC1003-CiM), University of Münster, 48149 Münster, Germany wedlich@uni-muenster.de.
Biologie cellulaire et Cancer · FRDynamique du noyau · FRMassachusetts Institute of Technology · USMax Planck Institute of Biochemistry · DEMax Planck Institute of Molecular Cell Biology and Genetics · DEUniversity of Münster · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although cortical actin plays an important role in cellular mechanics and morphogenesis, there is surprisingly little information on cortex organization at the apical surface of cells. In this paper, we characterize organization and dynamics of microvilli (MV) and a previously unappreciated actomyosin network at the apical surface of Madin-Darby canine kidney cells. In contrast to short and static MV in confluent cells, the apical surfaces of nonconfluent epithelial cells (ECs) form highly dynamic protrusions, which are often oriented along the plane of the membrane. These dynamic MV exhibit complex and spatially correlated reorganization, which is dependent on myosin II activity. Surprisingly, myosin II is organized into an extensive network of filaments spanning the entire apical membrane in nonconfluent ECs. Dynamic MV, myosin filaments, and their associated actin filaments form an interconnected, prestressed network. Interestingly, this network regulates lateral mobility of apical membrane probes such as integrins or epidermal growth factor receptors, suggesting that coordinated actomyosin dynamics contributes to apical cell membrane organization.

Indexed as

ActomyosinAnimalsCell Line, TumorCell MembraneCell PolarityCell ProliferationDogsEpithelial CellsEpitheliumHeLa CellsHepatocyte Growth FactorHeterocyclic Compounds, 4 or More RingsHumansIntercellular JunctionsMadin Darby Canine Kidney CellsMCF-7 CellsActomyosinblebbistatinHepatocyte Growth FactorHeterocyclic Compounds, 4 or More RingsMyosin Type II

Identifiers

PMID25313407
PMCPMC4195824
OpenAlexW1526240474

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.