Evidence map›Paper›PMID 21982379›Full record

ArticleBMC cell biology2011

Different modes of state transitions determine pattern in the Phosphatidylinositide-Actin system.

Günther Gerisch, Mary Ecke, Dirk Wischnewski, Britta Schroth-Diez

Open access · goldAbstract read
In one paragraph

Article in BMC cell biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

39 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Article
  3. Signaling and actin waves at a glance.Journal of cell science · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Nonlinear dynamics in phosphoinositide metabolism.Current opinion in cell biology · 2024
    Review
  8. Competition and Synergy of Arp2/3 and Formins in Nucleating Actin Waves.bioRxiv : the preprint server for biology · 2023
    Article
  9. Article
  10. Article
  11. Nanotopography modulates intracellular excitable systems through cytoskeleton actuation.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  12. Article
  13. Mechanochemical subcellular-element model of crawling cells.Frontiers in cell and developmental biology · 2022
    Article
  14. Gradients of PI(4,5)PFrontiers in cell and developmental biology · 2022
    Article
  15. Using Live-Cell Imaging and Synthetic Biology to Probe Directed Migration inFrontiers in cell and developmental biology · 2021
    Review
  16. How cortical waves drive fission of motile cells.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  17. Article
  18. Review
  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

4 authors at 2 institutions in 1 country.

Günther GerischMax Planck Institute of Biochemistry, Am Klopferspitz 18, 82152 Martinsried, Germany. gerisch@biochem.mpg.de
Mary Ecke
Dirk Wischnewski
Britta Schroth-Diez
Max Planck Institute of Biochemistry · DEMax Planck Institute of Molecular Cell Biology and Genetics · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn a motile polarized cell the actin system is differentiated to allow protrusion at the front and retraction at the tail. This differentiation is linked to the phosphoinositide pattern in the plasma membrane. In the highly motile Dictyostelium cells studied here, the front is dominated by PI3-kinases producing PI(3,4,5)tris-phosphate (PIP3), the tail by the PI3-phosphatase PTEN that hydrolyses PIP3 to PI(4,5)bis-phosphate. To study de-novo cell polarization, we first depolymerized actin and subsequently recorded the spontaneous reorganization of actin patterns in relation to PTEN.

resultsIn a transient stage of recovery from depolymerization, symmetric actin patterns alternate periodically with asymmetric ones. The switches to asymmetry coincide with the unilateral membrane-binding of PTEN. The modes of state transitions in the actin and PTEN systems differ. Transitions in the actin system propagate as waves that are initiated at single sites by the amplification of spontaneous fluctuations. In PTEN-null cells, these waves still propagate with normal speed but loose their regular periodicity. Membrane-binding of PTEN is induced at the border of a coherent PTEN-rich area in the form of expanding and regressing gradients.

conclusionsThe state transitions in actin organization and the reversible transition from cytoplasmic to membrane-bound PTEN are synchronized but their patterns differ. The transitions in actin organization are independent of PTEN, but when PTEN is present, they are coupled to periodic changes in the membrane-binding of this PIP3-degrading phosphatase. The PTEN oscillations are related to motility patterns of chemotaxing cells.

Indexed as

Actin CytoskeletonBiological ClocksCell MovementCell PolarityCells, CulturedCell Surface ExtensionsDictyosteliumGene Knockout TechniquesPhosphatidylinositol 3-KinasesProtein BindingProtein TransportPTEN PhosphohydrolasePhosphatidylinositol 3-KinasesPTEN Phosphohydrolase

Identifiers

PMID21982379
PMCPMC3199247
OpenAlexW2042692951

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.