Evidence map›Paper›PMID 21163521›Full record

ArticleBiomaterials2011

The regulation of traction force in relation to cell shape and focal adhesions.

Andrew D Rape, Wei-Hui Guo, Yu-Li Wang

Abstract read
In one paragraph

Article in Biomaterials, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 129 papers.

0numbers the graph read from it
0cells of the map it votes in
129citing 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

129 citing papers in PubMed.

  1. Article
  2. Article
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  5. Article
  6. Review
  7. Quantifying cell traction forces at the single-fiber scale in 3D: An approach based on deformable photopolymerized fiber arrays.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Cellular and Nuclear Forces: An Overview.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

69 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

3 authors.

Andrew D RapeDepartment of Biomedical Engineering, Carnegie Mellon University, PTC 4105-07, 700 Technology Drive, Pittsburgh, PA 15219, USA.
Wei-Hui Guo
Yu-Li Wang

Funding

DYNAMICS OF ACTIN IN NORMAL AND TRANSFORMED CELLSR37GM032476 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WANG, YU-LI · 1998 to 2007
$3.4M
DYNAMICS OF ACTIN STRUCTURES DURING CELL TRANSFORMATIONR01GM032476 · NIGMS · WORCESTER FOUNDATION FOR BIOMEDICAL RES · PI WANG, YU-LI · 1986 to 2011
$2.0M
NIGMS NIH HHS GM-32476NIGMS NIH HHS R01 GM032476NIGMS NIH HHS R37 GM032476
6 · The paper itself

Abstract

Mechanical forces provide critical inputs for proper cellular functions. The interplay between the generation of, and response to, mechanical forces regulate such cellular processes as differentiation, proliferation, and migration. We postulate that adherent cells respond to a number of physical and topographical factors, including cell size and shape, by detecting the magnitude and/or distribution of traction forces under different conditions. To address this possibility we introduce a new simple method for precise micropatterning of hydrogels, and then apply the technique to systematically investigate the relationship between cell geometry, focal adhesions, and traction forces in cells with a series of spread areas and aspect ratios. Contrary to previous findings, we find that traction force is not determined primarily by the cell spreading area but by the distance from cell center to the perimeter. This distance in turn controls traction forces by regulating the size of focal adhesions, such that constraining the size of focal adhesions by micropatterning can override the effect of geometry. We propose that the responses of traction forces to center-periphery distance, possibly through a positive feedback mechanism that regulates focal adhesions, provide the cell with the information on its own shape and size. A similar positive feedback control may allow cells to respond to a variety of physical or topographical signals via a unified mechanism.

Indexed as

Stress, MechanicalAcrylic ResinsAnimalsCell AdhesionCell Culture TechniquesCells, CulturedCell ShapeFocal AdhesionsHydrogelsMiceNIH 3T3 CellsPolyacrylamidesAcrylic ResinsHydrogelsPolyacrylamides

Identifiers

PMID21163521
PMCPMC3029020

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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.