Evidence map›Paper›PMID 30927191›Full record

ArticleBulletin of mathematical biology2019

Adapting a Plant Tissue Model to Animal Development: Introducing Cell Sliding into VirtualLeaf.

Henri B Wolff, Lance A Davidson, Roeland M H Merks

Abstract read
In one paragraph

Article in Bulletin of mathematical biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Modeling Plant Tissue Development Using VirtualLeaf.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  7. Review
  8. 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

3 authors.

Henri B WolffCentrum Wiskunde and Informatica, Science Park 123, 1098 XG, Amsterdam, The Netherlands.ORCID 0000-0003-3417-6955
Lance A DavidsonDepartments of Bioengineering, Developmental Biology, and Computational and Systems Biology, University of Pittsburgh, Bioscience Tower 3-5059 3501 Fifth Avenue, Pittsburgh, PA, USA. lad43@pitt.edu.ORCID 0000-0002-2956-0437
Roeland M H MerksCentrum Wiskunde and Informatica, Science Park 123, 1098 XG, Amsterdam, The Netherlands. merksrmh@math.leidenuniv.nl.ORCID 0000-0002-6152-687X

Funding

The Biomechanics of morphogenesis in the frogR01HD044750 · NICHD · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI DAVIDSON, LANCE A. · 2005 to 2020
$3.8M
Interaction between blood flow and ALK1 signaling in AVM developmentR01HL136566 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ROMAN, BETH L · 2017 to 2020
$1.7M
Mechanical Control of Mesenchymal-to-Epithelial TransitionR56HL134195 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DAVIDSON, LANCE A. · 2016 to 2016
$550k
Biophysics of development buffering: Temperature as a tool to study how the cytosR21ES019259 · NIEHS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DAVIDSON, LANCE A. · 2010 to 2011
$404k
NHLBI NIH HHS R01 HL136566NHLBI NIH HHS R56 HL134195NICHD NIH HHS R01 HD044750NIEHS NIH HHS R21 ES019259
6 · The paper itself

Abstract

Cell-based, mathematical modeling of collective cell behavior has become a prominent tool in developmental biology. Cell-based models represent individual cells as single particles or as sets of interconnected particles and predict the collective cell behavior that follows from a set of interaction rules. In particular, vertex-based models are a popular tool for studying the mechanics of confluent, epithelial cell layers. They represent the junctions between three (or sometimes more) cells in confluent tissues as point particles, connected using structural elements that represent the cell boundaries. A disadvantage of these models is that cell-cell interfaces are represented as straight lines. This is a suitable simplification for epithelial tissues, where the interfaces are typically under tension, but this simplification may not be appropriate for mesenchymal tissues or tissues that are under compression, such that the cell-cell boundaries can buckle. In this paper, we introduce a variant of VMs in which this and two other limitations of VMs have been resolved. The new model can also be seen as on off-the-lattice generalization of the Cellular Potts Model. It is an extension of the open-source package VirtualLeaf, which was initially developed to simulate plant tissue morphogenesis where cells do not move relative to one another. The present extension of VirtualLeaf introduces a new rule for cell-cell shear or sliding, from which cell rearrangement (T1) and cell extrusion (T2) transitions emerge naturally, allowing the application of VirtualLeaf to problems of animal development. We show that the updated VirtualLeaf yields different results than the traditional vertex-based models for differential adhesion-driven cell sorting and for the neighborhood topology of soft cellular networks.

Indexed as

Models, BiologicalMorphogenesisAnimalsBiomechanical PhenomenaCell AdhesionCell CommunicationCell MovementComputer SimulationDevelopmental BiologyEpithelial CellsEpitheliumMathematical ConceptsMonte Carlo MethodPlant DevelopmentSoftwareBubbly vertex modelCell-based modelingCell rearrangementCell sortingCellular Potts ModelDevelopmental biologyEpithelial morphogenesisEpithelial tissuesJunction remodelingVertex-based model

Identifiers

PMID30927191
PMCPMC6677868

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.