Evidence map›Paper›PMID 26744226›Full record

ArticleNature communications2016

Interplay of active processes modulates tension and drives phase transition in self-renewing, motor-driven cytoskeletal networks.

Michael Mak, Muhammad H Zaman, Roger D Kamm, Taeyoon Kim

Abstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing 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

55 citing papers in PubMed.

  1. Article
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  9. Review
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  12. Patterning of the cell cortex by Rho GTPases.Nature reviews. Molecular cell biology · 2024
    Review
  13. Article
  14. Article
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  16. Article
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  20. Age Dependent Changes in Corneal Epithelial Cell Signaling.Frontiers in cell and developmental biology · 2022
    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

4 authors.

Michael MakDepartment of Mechanical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, USA.
Muhammad H ZamanDepartment of Biomedical Engineering, Boston University, 44 Cummington Mall, Boston, Massachusetts 02215, USA.
Roger D KammDepartment of Mechanical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, USA.
Taeyoon KimWeldon School of Biomedical Engineering, Purdue University, 206 S. Martin Jischke Drive, West Lafayette, Indiana 47907, USA.

Funding

Modeling bi-directional signaling and cytoskeletal dynamics in 3D cell migrationsU01CA177799 · NCI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI GERTLER, FRANK B, KAMM, ROGER D · 2013 to 2017
$3.0M
Multiscale Analysis of Cancer Cell MechanicsF32CA196149 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI MAK, MICHAEL · 2015 to 2016
$98k
Howard Hughes Medical InstituteNCI NIH HHS 5U01CA177799NCI NIH HHS F32 CA196149NCI NIH HHS U01 CA177799
6 · The paper itself

Abstract

The actin cytoskeleton--a complex, nonequilibrium network consisting of filaments, actin-crosslinking proteins (ACPs) and motors--confers cell structure and functionality, from migration to morphogenesis. While the core components are recognized, much less is understood about the behaviour of the integrated, disordered and internally active system with interdependent mechano-chemical component properties. Here we use a Brownian dynamics model that incorporates key and realistic features--specifically actin turnover, ACP (un)binding and motor walking--to reveal the nature and underlying regulatory mechanisms of overarching cytoskeletal states. We generate multi-dimensional maps that show the ratio in activity of these microscopic elements determines diverse global stress profiles and the induction of nonequilibrium morphological phase transition from homogeneous to aggregated networks. In particular, actin turnover dynamics plays a prominent role in tuning stress levels and stabilizing homogeneous morphologies in crosslinked, motor-driven networks. The consequence is versatile functionality, from dynamic steady-state prestress to large, pulsed constrictions.

Indexed as

Actin CytoskeletonBridged Bicyclo Compounds, HeterocyclicCell Line, TumorCytochalasin DHumansMicroscopy, ConfocalMolecular Dynamics SimulationMolecular Motor ProteinsNucleic Acid Synthesis InhibitorsPhase TransitionStress, MechanicalThiazolidinesTime-Lapse ImagingBridged Bicyclo Compounds, HeterocyclicCytochalasin Dlatrunculin AMolecular Motor ProteinsNucleic Acid Synthesis InhibitorsThiazolidines

Identifiers

PMID26744226
PMCPMC4714927

What OpenQuestion holds

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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.