Evidence map›Paper›PMID 11739792›Full record

ArticleMolecular biology of the cell2001

Distinct roles of frontal and rear cell-substrate adhesions in fibroblast migration.

S Munevar, Y L Wang, M Dembo

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2001. 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
2.5field-weighted citation impact, top 12% 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

55 citing papers in PubMed, 138 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. TheAnatomy & cell biology · 2022
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Biophysics of Cell-Substrate Interactions Under Shear.Frontiers in cell and developmental biology · 2019
    Review
  14. Article
  15. Article
  16. Article
  17. Guidance of Axons by Local Coupling of Retrograde Flow to Point Contact Adhesions.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  18. Article
  19. Osteopontin is proteolytically processed by matrix metalloproteinase 9.Canadian journal of physiology and pharmacology · 2015
    Article
  20. Mechanotransduction in intervertebral discs.Journal of cellular and molecular medicine · 2014
    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

3 authors at 2 institutions in 1 country.

S MunevarDepartment of Physiology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Y L Wang
M Dembo
University of Massachusetts Chan Medical School · USBoston University · US

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
THE BIOPHYSICS OF CELL-SUBSTRATUM TRACTION STRESSR01GM061806 · NIGMS · BOSTON UNIVERSITY · PI DEMBO, MICAH · 2000 to 2003
$989k
MECHANICAL FORCES IN CELL MIGRATION AND CELL SIGNALINGF31GM020749 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI MUNEVAR, STEVEN · 2000 to 2000
$20k
NIGMS NIH HHS F31 GM020749NIGMS NIH HHS GM-20749NIGMS NIH HHS GM-32476NIGMS NIH HHS GM-61806NIGMS NIH HHS R01 GM032476NIGMS NIH HHS R01 GM061806NIGMS NIH HHS R37 GM032476
6 · The paper itself

Abstract

Cell migration involves complex physical and chemical interactions with the substrate. To probe the mechanical interactions under different regions of migrating 3T3 fibroblasts, we have disrupted cell-substrate adhesions by local application of the GRGDTP peptide, while imaging stress distribution on the substrate with traction force microscopy. Both spontaneous and GRGDTP-induced detachment of the trailing edge caused extensive cell shortening, without changing the overall level of traction forces or the direction of migration. In contrast, disruption of frontal adhesions caused dramatic, global loss of traction forces before any significant shortening of the cell. Although traction forces and cell migration recovered within 10-20 min of transient frontal treatment, persistent treatment with GRGDTP caused the cell to develop traction forces elsewhere and reorient toward a new direction. We conclude that contractile forces of a fibroblast are transmitted to the substrate through two distinct types of adhesions. Leading edge adhesions are unique in their ability to transmit active propulsive forces. Their functions cannot be transferred directly to existing adhesions upon detachment. Trailing end adhesions create passive resistance during cell migration and readily redistribute their loads upon detachment. Our results indicate the distinct nature of mechanical interactions at the leading versus trailing edges, which together generate the mechanical interactions for fibroblast migration.

Indexed as

Cell Movement3T3 CellsAnimalsBiomechanical PhenomenaCell AdhesionFibroblastsMiceMicroscopy, Phase-ContrastOligopeptidesTime Factorsfibronectin attachment peptideOligopeptidesNon-programmatic

Identifiers

PMID11739792
PMCPMC60767
OpenAlexW2152002201

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.