Evidence map›Paper›PMID 16100274›Full record

ArticleBiophysical journal2005

Periodic patterns of actin turnover in lamellipodia and lamellae of migrating epithelial cells analyzed by quantitative Fluorescent Speckle Microscopy.

A Ponti, A Matov, M Adams, S Gupton, C M Waterman-Storer, G Danuser

Abstract read
In one paragraph

Article in Biophysical journal, 2005. 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
–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

55 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Modulation of the cytoskeleton for cancer therapy.Frontiers in cell and developmental biology · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Bioimage Analysis and Cell Motility.Patterns (New York, N.Y.) · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Discovery of functional interactions among actin regulators by analysis of image fluctuations in an unperturbed motile cell system.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Review
  15. Article
  16. Article
  17. Intrinsic activity in cells and the brain.Molecular biology of the cell · 2014
    Article
  18. Article
  19. Article
  20. Dynamic and reversible surface topography influences cell morphology.Journal of biomedical materials research. Part A · 2013
    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

6 authors.

A PontiDepartment of Cell Biology, The Scripps Research Institute, La Jolla, California, USA.
A Matov
M Adams
S Gupton
C M Waterman-Storer
G Danuser

Funding

Quantitative Fluorescent Speckle MicroscopyR01GM067230 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI DANUSER, GAUDENZ · 2003 to 2019
$3.3M
NIGMS NIH HHS R01 GM067230NIGMS NIH HHS R01 GM 67230
6 · The paper itself

Abstract

We measured actin turnover in lamellipodia and lamellae of migrating cells, using quantitative Fluorescent Speckle Microscopy. Lamellae disassembled at low rates from the front to the back. However, the dominant feature in their turnover was a spatially random pattern of periodic polymerization and depolymerization moving with the retrograde flow. Power spectra contained frequencies between 0.5 and 1 cycle/min. The spectra remained unchanged when applying Latrunculin A and Jasplakinolide in low doses, except that additional frequencies occurred beyond 1 cycle/min. Whereas Latrunculin did not change the rate of mean disassembly, Jasplakinolide halted it completely, indicating that the steady state and the dynamics of actin turnover are differentially affected by pharmacological agents. Lamellipodia assembled in recurring bursts at the leading edge and disassembled approximately 2.5 microm behind. Events of polymerization correlated spatially and temporally with transient formation of Arp2/3 clusters. In lamellae, Arp2/3 accumulation and polymerization correlated only spatially, suggesting an Arp2/3-independent mechanism for filament nucleation. To acquire these data we had to enhance the resolution of quantitative Fluorescent Speckle Microscopy to the submicron level. Several algorithmic advances in speckle image processing are described enabling the analysis of kinetic and kinematic activities of polymer networks at the level of single speckles.

Indexed as

Actin-Related Protein 2Actin-Related Protein 3ActinsAlgorithmsAnimalsBiophysicsBridged Bicyclo Compounds, HeterocyclicCell LineCell MovementCells, CulturedDepsipeptidesEpithelial CellsImage Processing, Computer-AssistedKineticsMicroscopy, ConfocalMicroscopy, FluorescenceActin-Related Protein 2Actin-Related Protein 3ActinsBridged Bicyclo Compounds, HeterocyclicDepsipeptidesjasplakinolidelatrunculin APolymersThiazolesThiazolidines

Identifiers

PMID16100274
PMCPMC1366841

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.