Evidence map›Paper›PMID 25908864›Full record

ArticleJournal of cell science2015

Traction forces mediated by integrin signaling are necessary for definitive endoderm specification.

Hermes Taylor-Weiner, Neeraja Ravi, Adam J Engler

Abstract read
In one paragraph

Article in Journal of cell science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Mechanically guided cell fate determination in early development.Cellular and molecular life sciences : CMLS · 2024
    Review
  3. A Hierarchical Mechanotransduction System: From Macro to Micro.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Interplay between mechanics and signalling in regulating cell fate.Nature reviews. Molecular cell biology · 2022
    Review
  10. Emerging Role of Mechanical Forces in Cell Fate Acquisition.Frontiers in cell and developmental biology · 2022
    Review
  11. Dose-Extreme Mechanics Letters · 2021
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. 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.

Hermes Taylor-WeinerDepartment of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA Sanford Consortium for Regenerative Medicine, La Jolla, CA 92037, USA.
Neeraja RaviDepartment of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA.
Adam J EnglerDepartment of Bioengineering, University of California, San Diego, La Jolla, CA 92093, USA Sanford Consortium for Regenerative Medicine, La Jolla, CA 92037, USA Biomedical Sciences Program, University of California, San Diego, La Jolla, CA 92093, USA aengler@ucsd.edu.

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Ye Zheng · 1985 to 2026
$82.8M
Salk Institute for Biological Studies NINDS Center Core GrantP30NS072031 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI O'LEARY, DENNIS D · 2011 to 2015
$4.2M
"Smart" Materials to Engineer a More Complete Stem Cell NicheDP2OD006460 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ENGLER, ADAM J · 2009 to 2009
$2.3M
Improving Endoderm Specification with Hybrid Materials and Growth FactorsR21EB011727 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ENGLER, ADAM J · 2010 to 2011
$351k
NCI NIH HHS CA014195-50NCI NIH HHS P30 CA014195NIBIB NIH HHS R21 EB011727NIBIB NIH HHS R21EB011727NIH HHS DP02OD006460NIH HHS DP2 OD006460NINDS NIH HHS NS072031-03A1NINDS NIH HHS P30 NS072031
6 · The paper itself

Abstract

Pluripotent embryonic stem cells (ESCs) exert low-traction forces on their niche in vitro whereas specification to definitive endoderm in vivo coincides with force-mediated motility, suggesting a differentiation-mediated switch. However, the onset of contractility and extent to which force-mediated integrin signaling regulates fate choices is not understood. To address the requirement of tractions forces for differentiation, we examined mouse embryonic stem cell (ESC) specification towards definitive endoderm on fibrillar fibronectin containing a deformation-sensitive FRET probe. Inhibiting contractility resulted in an increase in the observed fibronectin FRET intensity ratio but also decreased the amount of phosphorylated nuclear SMAD2, leading to reduced expression of the definitive endoderm marker SOX17. By contrast ESCs maintained in pluripotency medium did not exert significant tractions against the fibronectin matrix. When laminin-111 was added to fibrillar matrices to improve the efficiency of definitive endoderm induction, ESCs decreased their fibronectin traction forces in a laminin-dependent manner; blocking the laminin-binding α3-integrin restored fibronectin matrix deformation and reduced SOX17 expression and SMAD2 phosphorylation, probably because of compensation of inhibitory signaling from SMAD7 after 5 days in culture. These data imply that traction forces and integrin signaling are important regulators of early fate decisions in ESCs.

Indexed as

AnimalsCell DifferentiationEmbryonic Stem CellsEndodermHumansIntegrinsMicePluripotent Stem CellsProtein BindingSignal TransductionIntegrinsEmbryonic stem cellsEndodermExtracellular matrixIntegrin signalingSMAD

Identifiers

PMID25908864
PMCPMC4457159

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.