Evidence map›Paper›PMID 22447948›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2012

Flow mechanotransduction regulates traction forces, intercellular forces, and adherens junctions.

Lucas H Ting, Jessica R Jahn, Joon I Jung, Benjamin R Shuman, Shirin Feghhi, Sangyoon J Han, Marita L Rodriguez, Nathan J Sniadecki

Abstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

39 citing papers in PubMed, 85 citations in OpenAlex.

  1. Gene-Specific Endothelial Programs Drive AVM Pathogenesis inArteriosclerosis, thrombosis, and vascular biology · 2026
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  7. Frontiers in microbiology · 2022
    Article
  8. Article
  9. Potential Therapeutic Applications of N-Cadherin Antagonists and Agonists.Frontiers in cell and developmental biology · 2022
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. The Importance of Mechanical Forces forFrontiers in physiology · 2020
    Review
  15. Article
  16. Article
  17. Biophysics of Cell-Substrate Interactions Under Shear.Frontiers in cell and developmental biology · 2019
    Review
  18. Review
  19. Article
  20. Review of cellular mechanotransduction on micropost substrates.Medical & biological engineering & computing · 2016
    Review
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

8 authors at 1 institution in 1 country.

Lucas H TingDepartment of Mechanical Engineering, University of Washington, Seattle, 98195, USA.
Jessica R Jahn
Joon I Jung
Benjamin R Shuman
Shirin Feghhi
Sangyoon J Han
Marita L Rodriguez
Nathan J Sniadecki
University of Washington · US

Funding

Bioengineering Cardiovascular Training GrantT32EB001650 · NIBIB · UNIVERSITY OF WASHINGTON · PI REGNIER, MICHAEL · 2004 to 2019
$3.6M
Subcellular Platelet Forces and AdhesionsR21HL097284 · NHLBI · UNIVERSITY OF WASHINGTON · PI SNIADECKI, NATHAN JOHN · 2009 to 2010
$394k
NHLBI NIH HHS HL-097284NIBIB NIH HHS EB-001650NIBIB NIH HHS T32 EB001650
6 · The paper itself

Abstract

Endothelial cells respond to fluid shear stress through mechanotransduction responses that affect their cytoskeleton and cell-cell contacts. Here, endothelial cells were grown as monolayers on arrays of microposts and exposed to laminar or disturbed flow to examine the relationship among traction forces, intercellular forces, and cell-cell junctions. Cells under laminar flow had traction forces that were higher than those under static conditions, whereas cells under disturbed flow had lower traction forces. The response in adhesion junction assembly matched closely with changes in traction forces since adherens junctions were larger in size for laminar flow and smaller for disturbed flow. Treating the cells with calyculin-A to increase myosin phosphorylation and traction forces caused an increase in adherens junction size, whereas Y-27362 cause a decrease in their size. Since tugging forces across cell-cell junctions can promote junctional assembly, we developed a novel approach to measure intercellular forces and found that these forces were higher for laminar flow than for static or disturbed flow. The size of adherens junctions and tight junctions matched closely with intercellular forces for these flow conditions. These results indicate that laminar flow can increase cytoskeletal tension while disturbed flow decreases cytoskeletal tension. Consequently, we found that changes in cytoskeletal tension in response to shear flow conditions can affect intercellular tension, which in turn regulates the assembly of cell-cell junctions.

Indexed as

Adherens JunctionsAmidesCell CommunicationCells, CulturedCytoskeletonEndothelium, VascularHumansMarine ToxinsMechanotransduction, CellularMuscle Relaxants, CentralOxazolesPulmonary ArteryPyridinesShear StrengthVasoconstrictor AgentsAmidescalyculin AMarine ToxinsMuscle Relaxants, CentralOxazolesPyridinesVasoconstrictor AgentsY 27632

Identifiers

PMID22447948
PMCPMC3378295
OpenAlexW2123330453

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.