Evidence map›Paper›PMID 29490253›Full record

ArticleBiophysical journal2018

Spatial Fluctuations at Vertices of Epithelial Layers: Quantification of Regulation by Rho Pathway.

Étienne Fodor, Vishwajeet Mehandia, Jordi Comelles, Raghavan Thiagarajan, Nir S Gov, Paolo Visco, Frédéric van Wijland, Daniel Riveline

Abstract read
In one paragraph

Article in Biophysical journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Sculpting tissues by phase transitions.Nature communications · 2022
    Review
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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

8 authors.

Étienne FodorDAMTP, Centre for Mathematical Sciences, University of Cambridge, Cambridge, United Kingdom; Laboratoire Matière et Systèmes Complexes, UMR 7057 CNRS/P7, Université Paris Diderot, Paris cedex 13, France.
Vishwajeet MehandiaLaboratory of Cell Physics, ISIS/IGBMC, Université de Strasbourg and CNRS (UMR 7006), Strasbourg, France; Development and Stem Cells Program, IGBMC, CNRS (UMR 7104), INSERM (U964), Université de Strasbourg, Illkirch, France; School of Mechanical, Materials and Energy Engineering, Indian Institute of Technology, Ropar, India.
Jordi ComellesLaboratory of Cell Physics, ISIS/IGBMC, Université de Strasbourg and CNRS (UMR 7006), Strasbourg, France; Development and Stem Cells Program, IGBMC, CNRS (UMR 7104), INSERM (U964), Université de Strasbourg, Illkirch, France.
Raghavan ThiagarajanLaboratory of Cell Physics, ISIS/IGBMC, Université de Strasbourg and CNRS (UMR 7006), Strasbourg, France; Development and Stem Cells Program, IGBMC, CNRS (UMR 7104), INSERM (U964), Université de Strasbourg, Illkirch, France.
Nir S GovDepartment of Chemical Physics, Weizmann Institute of Science, Rehovot, Israel.
Paolo ViscoLaboratoire Matière et Systèmes Complexes, UMR 7057 CNRS/P7, Université Paris Diderot, Paris cedex 13, France.
Frédéric van WijlandLaboratoire Matière et Systèmes Complexes, UMR 7057 CNRS/P7, Université Paris Diderot, Paris cedex 13, France.
Daniel RivelineLaboratory of Cell Physics, ISIS/IGBMC, Université de Strasbourg and CNRS (UMR 7006), Strasbourg, France; Development and Stem Cells Program, IGBMC, CNRS (UMR 7104), INSERM (U964), Université de Strasbourg, Illkirch, France. Electronic address: riveline@unistra.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In living matter, shape fluctuations induced by acto-myosin are usually studied in vitro via reconstituted gels, whose properties are controlled by changing the concentrations of actin, myosin, and cross-linkers. Such an approach deliberately avoids consideration of the complexity of biochemical signaling inherent to living systems. Acto-myosin activity inside living cells is mainly regulated by the Rho signaling pathway, which is composed of multiple layers of coupled activators and inhibitors. Here, we investigate how such a pathway controls the dynamics of confluent epithelial tissues by tracking the displacements of the junction points between cells. Using a phenomenological model to analyze the vertex fluctuations, we rationalize the effects of different Rho signaling targets on the emergent tissue activity by quantifying the effective diffusion coefficient, and the persistence time and length of the fluctuations. Our results reveal an unanticipated correlation between layers of activation/inhibition and spatial fluctuations within tissues. Overall, this work connects regulation via biochemical signaling with mesoscopic spatial fluctuations, with potential application to the study of structural rearrangements in epithelial tissues.

Indexed as

ActomyosinAnimalsDogsEpithelial CellsKidneyMadin Darby Canine Kidney Cellsrho GTP-Binding ProteinsSignal TransductionActomyosinrho GTP-Binding Proteins

Identifiers

PMID29490253
PMCPMC5984978

What OpenQuestion holds

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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.