Evidence map›Paper›PMID 31229244›Full record

ArticleBiophysical journal2019

Elongated Cells Drive Morphogenesis in a Surface-Wrapped Finite-Element Model of Germband Retraction.

W Tyler McCleery, Jim Veldhuis, Monica E Bennett, Holley E Lynch, Xiaoyan Ma, G Wayne Brodland, M Shane Hutson

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 3 institutions in 2 countries.

W Tyler McCleeryDepartment of Physics & Astronomy, Vanderbilt University, Nashville, Tennessee.
Jim VeldhuisDepartment of Civil & Environmental Engineering, University of Waterloo, Waterloo, Ontario, Canada.
Monica E BennettDepartment of Physics & Astronomy, Vanderbilt University, Nashville, Tennessee.
Holley E LynchDepartment of Physics, Stetson University, DeLand, Florida.
Xiaoyan MaDepartment of Physics & Astronomy, Vanderbilt University, Nashville, Tennessee.
G Wayne BrodlandDepartment of Civil & Environmental Engineering, University of Waterloo, Waterloo, Ontario, Canada.
M Shane HutsonDepartment of Physics & Astronomy, Vanderbilt University, Nashville, Tennessee; Department of Biological Sciences, Vanderbilt University, Nashville, Tennessee. Electronic address: shane.hutson@vanderbilt.edu.
Vanderbilt University · USUniversity of Waterloo · CAStetson University · US

Funding

Cellular Biomechanics of Heat-Shock Induced Defects in Drosophila EmbryogenesisR01GM099107 · NIGMS · VANDERBILT UNIVERSITY · PI BRODLAND, GERALD WAYNE, HUTSON, M. SHANE · 2011 to 2014
$1.1M
NIGMS NIH HHS R01 GM099107
6 · The paper itself

Abstract

During Drosophila embryogenesis, the germband first extends to curl around the posterior end of the embryo and then retracts back; however, retraction is not simply the reversal of extension. At a tissue level, extension is coincident with ventral furrow formation, and at a cellular level, extension occurs via convergent cell neighbor exchanges in the germband, whereas retraction involves only changes in cell shape. To understand how cell shapes, tissue organization, and cellular forces drive germband retraction, we investigate this process using a whole-embryo, surface-wrapped cellular finite-element model. This model represents two key epithelial tissues-amnioserosa and germband-as adjacent sheets of two-dimensional cellular finite elements that are wrapped around an ellipsoidal three-dimensional approximation of an embryo. The model reproduces the detailed kinematics of in vivo retraction by fitting just one free model parameter, the tension along germband cell interfaces; all other cellular forces are constrained to follow ratios inferred from experimental observations. With no additional parameter adjustments, the model also reproduces quantitative assessments of mechanical stress using laser dissection and failures of retraction when amnioserosa cells are removed via mutations or microsurgery. Surprisingly, retraction in the model is robust to changes in cellular force values but is critically dependent on starting from a configuration with highly elongated amnioserosa cells. Their extreme cellular elongation is established during the prior process of germband extension and is then used to drive retraction. The amnioserosa is the one tissue whose cellular morphogenesis is reversed from germband extension to retraction, and this reversal coordinates the forces needed to retract the germband back to its pre-extension position and shape. In this case, cellular force strengths are less important than the carefully established cell shapes that direct them. VIDEO ABSTRACT.

Indexed as

Models, TheoreticalMorphogenesisAnimalsBiomechanical PhenomenaCell ShapeDrosophilaEpitheliumFinite Element AnalysisStress, Mechanical

Identifiers

PMID31229244
PMCPMC6626845
OpenAlexW2949898427

What OpenQuestion holds

Textmetadata
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.