Evidence map›Paper›PMID 24331927›Full record

ArticleDevelopmental cell2013

FHOD1 is needed for directed forces and adhesion maturation during cell spreading and migration.

Thomas Iskratsch, Cheng-Han Yu, Anurag Mathur, Shuaimin Liu, Virginie Stévenin, Joseph Dwyer, James Hone, Elisabeth Ehler, Michael Sheetz

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

67 citing papers in PubMed, 113 citations in OpenAlex.

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  13. FHODs: Nuclear tethered formins for nuclear mechanotransduction.Frontiers in cell and developmental biology · 2023
    Review
  14. Article
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  19. LSP1-myosin1e bimolecular complex regulates focal adhesion dynamics and cell migration.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  20. Article

7 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 3 countries.

Thomas IskratschDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA. Electronic address: ti2170@columbia.edu.
Cheng-Han YuMechanobiology Institute, National University of Singapore, Singapore 117411, Singapore.
Anurag MathurDepartment of Mechanical Engineering, Columbia University, New York, NY 10027, USA.
Shuaimin LiuDepartment of Mechanical Engineering, Columbia University, New York, NY 10027, USA.
Virginie StéveninDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA.
Joseph DwyerRandall Division of Cell and Molecular Biophysics and Cardiovascular Division, King's College London, London SE1 1UL, UK.
James HoneDepartment of Mechanical Engineering, Columbia University, New York, NY 10027, USA.
Elisabeth EhlerRandall Division of Cell and Molecular Biophysics and Cardiovascular Division, King's College London, London SE1 1UL, UK.
Michael SheetzDepartment of Biological Sciences, Columbia University, New York, NY 10027, USA; Mechanobiology Institute, National University of Singapore, Singapore 117411, Singapore. Electronic address: ms2001@columbia.edu.
Columbia University · USKing's College London · GBNational University of Singapore · SG

Funding

Nanomedicine development center for mechanobiologyPN2EY016586 · NEI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL LORAN · 2005 to 2014
$23.0M
Mechanisms of mechanical transduction by cytoskeletonsR01EB001480 · NIBIB · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI SHEETZ, MICHAEL PATRICK · 2003 to 2012
$3.0M
Center for Mechanotransduction and Nanomedicine. (RMI)PN1EY016586 · NEI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI SHEETZ, MICHAEL PATRICK · 2004 to 2004
$81k
NEI NIH HHS EY016586NEI NIH HHS PN1 EY016586NEI NIH HHS PN2 EY016586NIBIB NIH HHS EB001480NIBIB NIH HHS R01 EB001480
6 · The paper itself

Abstract

Matrix adhesions provide critical signals for cell growth or differentiation. They form through a number of distinct steps that follow integrin binding to matrix ligands. In an early step, integrins form clusters that support actin polymerization by an unknown mechanism. This raises the question of how actin polymerization occurs at the integrin clusters. We report here that a major formin in mouse fibroblasts, FHOD1, is recruited to integrin clusters, resulting in actin assembly. Using cell-spreading assays on lipid bilayers, solid substrates, and high-resolution force-sensing pillar arrays, we find that knockdown of FHOD1 impairs spreading, coordinated application of adhesive force, and adhesion maturation. Finally, we show that targeting of FHOD1 to the integrin sites depends on the direct interaction with Src family kinases and is upstream of the activation by Rho kinase. Thus, our findings provide insights into the mechanisms of cell migration with implications for development and disease.

Indexed as

Actin CytoskeletonAmino Acid SequenceAnimalsCell AdhesionCell MovementFemaleFetal ProteinsFetusFibroblastsFocal AdhesionsForminsGene Knockdown TechniquesIntegrinsMiceMolecular Sequence DataNuclear ProteinsFetal ProteinsFHOD1 protein, mouseForminsIntegrinsNuclear ProteinsRNA, Small Interferingsrc-Family Kinases

Identifiers

PMID24331927
PMCPMC3890431
OpenAlexW2009482382

What OpenQuestion holds

Textmetadata
LicenceTDM
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.