Evidence map›Paper›PMID 1874793›Full record

ArticleThe Journal of cell biology1991

The role of solation-contraction coupling in regulating stress fiber dynamics in nonmuscle cells.

J Kolega, L W Janson, D L Taylor

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 84 citations in OpenAlex.

  1. Tubulin Acetylation and the Cellular Mechanosensing and Stress Response.Results and problems in cell differentiation · 2025
    Review
  2. Article
  3. Review
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  8. Review
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  10. Mechanics rules cell biology.Sports medicine, arthroscopy, rehabilitation, therapy & technology : SMARTT · 2010
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Keratocytes generate traction forces in two phases.Molecular biology of the cell · 1999
    Article
  18. Article
  19. Article
  20. 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 at 1 institution in 1 country.

J KolegaDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213.
L W Janson
D L Taylor
Carnegie Mellon University · US

Funding

STRUCTURAL/CHEMICAL DYNAMICS OF CELL MOVEMENTR37AR032461 · NIAMS · CARNEGIE-MELLON UNIVERSITY · PI TAYLOR, D. LANSING · 1991 to 2000
$257k
APPLICATIONS OF FLUORESCENCE TECHNIQUES IN CELL BIOLOGYP01GM034639 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI TAYLOR, D. LANSING · 1985 to 1989
–
STRUCTURAL AND CHEMICAL DYNAMICS OF CELL MOVEMENTR01AR032461 · NIAMS · CARNEGIE-MELLON UNIVERSITY · PI TAYLOR, D. LANSING · 1986 to 1990
–
PREDOCTORAL TRAINING IN CELLULAR AND MOLECULAR BIOLOGYT32GM008067 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI JONES, ELIZABETH W · 1985 to 1992
–
NIAMS NIH HHS AR-32461NIGMS NIH HHS 5T32GM08067-08NIGMS NIH HHS GM-34639
6 · The paper itself

Abstract

Serum-deprived Swiss 3T3 fibroblasts constitutively form stress fibers at their edges. These fibers move centripetally towards the perinuclear region where they disassemble. Serum stimulation causes shortening of fibers in a manner suggesting active actin-myosin-based contraction (Giuliano, K.A. and D.L. Taylor. 1990. Cell Motil. and Cytoskeleton. 16:14-21). To elucidated the role of actin-based gel structure in these movements, we examined the effects of disrupting actin organization with cytochalasin. Serum-deprived fibroblasts were microinjected with rhodamine analogs of actin or myosin II and fiber dynamics were monitored with a multimode light microscope workstation using video-enhanced contrast and fluorescence modes. When cells were perfused with greater than or equal to 3 microM cytochalasin B or 0.5 microM cytochalasin D, formation and transport of stress fibers were reversibly inhibited, and rapid and immediate shortening of existing fibers was induced. Quantification of actin and myosin II fluorescence associated with individual shortening fibers demonstrated that fluorescence per length of fiber increased for both components, suggesting sliding filament contraction. However, there was also a net loss of both actin and myosin II from fibers as they shortened, indicating a self-destructive process. Loss of material from fibers coupled with increased overlap of actin and myosin II remaining in the fibers suggested that contraction could be induced not only by increasing the force exerted by contractile motors, but also by decreasing gel structure through partial solation. Finally, cytochalasin accelerated contraction of actin-myosin-based gels reconstituted from purified proteins in the absence of myosin-based regulation, further supporting solation-contraction coupling as a possible mechanism for modulating cytoplasmic contractility (Taylor, D.L. and M. Fechheimer. 1982. Philos. Trans. R. Soc. Lond. B. Biol. Sci. 299:185-197).

Indexed as

Actin CytoskeletonActinsActomyosinAnimalsCell LineCell MovementCytochalasinsFluorescent Antibody TechniqueGelsMiceMyosinsSolubilityActinsActomyosinCytochalasinsGelsMyosins

Identifiers

PMID1874793
PMCPMC2289116
OpenAlexW2033401525

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.