Evidence map›Paper›PMID 28114384›Full record

ArticlePLoS computational biology2017

Morphological Transformation and Force Generation of Active Cytoskeletal Networks.

Tamara Carla Bidone, Wonyeong Jung, Daniel Maruri, Carlos Borau, Roger D Kamm, Taeyoon Kim

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 62 citations in OpenAlex.

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  17. Tools for computational analysis of moving boundary problems in cellular mechanobiology.Wiley interdisciplinary reviews. Systems biology and medicine · 2020
    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

6 authors at 4 institutions in 3 countries.

Tamara Carla BidoneDepartment of Mechanical and Aerospace Engineering, Polytechnic University of Turin, Turin, Italy.ORCID 0000-0002-7096-4839
Wonyeong JungSchool of Mechanical Engineering, Purdue University, West Lafayette, Indiana, United States of America.
Daniel MaruriWeldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana, United States of America.
Carlos BorauDepartment of Mechanical Engineering, Aragon Institute of Engineering Research (I3A), University of Zaragoza, Zaragoza, Spain.ORCID 0000-0002-3784-1140
Roger D KammDepartments of Biological Engineering and Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
Taeyoon KimWeldon School of Biomedical Engineering, Purdue University, West Lafayette, Indiana, United States of America.ORCID 0000-0002-5588-8532
Purdue University West Lafayette · USMassachusetts Institute of Technology · USPolitecnico di Torino · ITUniversidad de Zaragoza · ES

Funding

Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
NCATS NIH HHS UL1 TR001108
6 · The paper itself

Abstract

Cells assemble numerous types of actomyosin bundles that generate contractile forces for biological processes, such as cytokinesis and cell migration. One example of contractile bundles is a transverse arc that forms via actomyosin-driven condensation of actin filaments in the lamellipodia of migrating cells and exerts significant forces on the surrounding environments. Structural reorganization of a network into a bundle facilitated by actomyosin contractility is a physiologically relevant and biophysically interesting process. Nevertheless, it remains elusive how actin filaments are reoriented, buckled, and bundled as well as undergo tension buildup during the structural reorganization. In this study, using an agent-based computational model, we demonstrated how the interplay between the density of myosin motors and cross-linking proteins and the rigidity, initial orientation, and turnover of actin filaments regulates the morphological transformation of a cross-linked actomyosin network into a bundle and the buildup of tension occurring during the transformation.

Indexed as

Models, BiologicalActin CytoskeletonActomyosinAnimalsComputer SimulationCytoskeletal ProteinsCytoskeletonElastic ModulusHumansMechanotransduction, CellularMolecular Motor ProteinsMorphogenesisStress, MechanicalActomyosinCytoskeletal ProteinsMolecular Motor Proteins

Identifiers

PMID28114384
PMCPMC5256887
OpenAlexW2581379811

What OpenQuestion holds

Textmetadata
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.