Evidence map›Paper›PMID 27074136›Full record

ArticlePLoS computational biology2016

Mechanical Stress Induces Remodeling of Vascular Networks in Growing Leaves.

Yohai Bar-Sinai, Jean-Daniel Julien, Eran Sharon, Shahaf Armon, Naomi Nakayama, Mokhtar Adda-Bedia, Arezki Boudaoud

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

7 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Article
  3. Growth couples temporal and spatial fluctuations of tissue properties during morphogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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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

7 authors at 4 institutions in 4 countries.

Yohai Bar-SinaiDepartment of Chemical Physics, Weizmann Institute of Science, Rehovot, Israel.
Jean-Daniel JulienLaboratoire de Physique, ENS Lyon, CNRS, UCB Lyon I, Université de Lyon, Lyon, France.
Eran SharonRacah Institute of Physics, The Hebrew University, Jerusalem, Israel.
Shahaf ArmonRacah Institute of Physics, The Hebrew University, Jerusalem, Israel.
Naomi NakayamaInstitute of Molecular Plant Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Mokhtar Adda-BediaLaboratoire de Physique Statistique, Ecole Normale Supérieure, CNRS, Université Paris VI, Université Paris VII, Paris, France.
Arezki BoudaoudLaboratoire Reproduction et Développement des Plantes, Univ Lyon, ENS de Lyon, UCB Lyon 1, CNRS, INRA, Lyon, France.
Centre National de la Recherche Scientifique · FRHebrew University of Jerusalem · ILUniversité Claude Bernard Lyon 1 · FREdinburgh College · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Differentiation into well-defined patterns and tissue growth are recognized as key processes in organismal development. However, it is unclear whether patterns are passively, homogeneously dilated by growth or whether they remodel during tissue expansion. Leaf vascular networks are well-fitted to investigate this issue, since leaves are approximately two-dimensional and grow manyfold in size. Here we study experimentally and computationally how vein patterns affect growth. We first model the growing vasculature as a network of viscoelastic rods and consider its response to external mechanical stress. We use the so-called texture tensor to quantify the local network geometry and reveal that growth is heterogeneous, resembling non-affine deformations in composite materials. We then apply mechanical forces to growing leaves after veins have differentiated, which respond by anisotropic growth and reorientation of the network in the direction of external stress. External mechanical stress appears to make growth more homogeneous, in contrast with the model with viscoelastic rods. However, we reconcile the model with experimental data by incorporating randomness in rod thickness and a threshold in the rod growth law, making the rods viscoelastoplastic. Altogether, we show that the higher stiffness of veins leads to their reorientation along external forces, along with a reduction in growth heterogeneity. This process may lead to the reinforcement of leaves against mechanical stress. More generally, our work contributes to a framework whereby growth and patterns are coordinated through the differences in mechanical properties between cell types.

Indexed as

Models, BiologicalAnisotropyArabidopsisBiomechanical PhenomenaBody PatterningComputational BiologyComputer SimulationPlant LeavesPlant Vascular BundleStress, Mechanical

Identifiers

PMID27074136
PMCPMC4830508
OpenAlexW2338354052

What OpenQuestion holds

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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.