Evidence map›Paper›PMID 18560567›Full record

ArticlePloS one2008

Formin 1-isoform IV deficient cells exhibit defects in cell spreading and focal adhesion formation.

Markus Dettenhofer, Fen Zhou, Philip Leder

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 39 citations in OpenAlex.

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  13. A nucleator arms race: cellular control of actin assembly.Nature reviews. Molecular cell biology · 2010
    Review
  14. Review
  15. Formins and microtubules.Biochimica et biophysica acta · 2010
    Review
  16. Review
  17. 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.

Markus DettenhoferDepartment of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.
Fen Zhou
Philip Leder
Harvard University · US

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

backgroundRegulation of the cytoskeleton is a central feature of cell migration. The formin family of proteins controls the rate of actin nucleation at its barbed end. Thus, formins are predicted to contribute to several important cell processes such as locomotion, membrane ruffling, vesicle endocytosis, and stress fiber formation and disassociation. METHODOLOGY/PRINCIPAL

findingsIn this study we investigated the functional role of Formin1-isoform4 (Fmn1-IV) by using genetically null primary cells that displayed augmented protrusive behaviour during wound healing and delayed cell spreading. Cells deficient of Fmn1-IV also showed reduced efficiency of focal adhesion formation. Additionally, we generated an enhanced green fluorescence protein (EGFP)-fused Fmn1-IV knock-in mouse to monitor the endogenous subcellular localization of Fmn1-IV. Its localization was found within the cytoplasm and along microtubules, yet it was largely excluded from adherens junctions. CONCLUSIONS/SIGNIFICANCE: It was determined that Fmn1-IV, as an actin nucleator, contributes to protrusion of the cell's leading edge and focal adhesion formation, thus contributing to cell motility.

Indexed as

AnimalsBase SequenceCell LineCell MovementDNA PrimersFetal ProteinsFluorescent Antibody TechniqueForminsGreen Fluorescent ProteinsMiceMice, TransgenicMicrofilament ProteinsMicroscopy, ElectronNuclear ProteinsProtein IsoformsDNA PrimersFetal ProteinsForminsGreen Fluorescent ProteinsMicrofilament ProteinsNuclear ProteinsProtein Isoforms

Identifiers

PMID18560567
PMCPMC2423616
OpenAlexW2068035706

What OpenQuestion holds

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LicenceCC BY
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.