Evidence map›Paper›PMID 36912152›Full record

ArticleThe EMBO journal2023

Recycling of the actin monomer pool limits the lifetime of network turnover.

Alexandra Colin, Tommi Kotila, Christophe Guérin, Magali Orhant-Prioux, Benoit Vianay, Alex Mogilner, Pekka Lappalainen, Manuel Théry, Laurent Blanchoin

Abstract read
In one paragraph

Article in The EMBO journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Filament transport supports contractile steady states of actin networks.bioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. MARCKS and PI(4,5)PMolecular biology of the cell · 2024
    Article
  10. Article
  11. Mechanisms of actin disassembly and turnover.The Journal of cell biology · 2023
    Review
  12. Article
  13. Article
  14. Friction patterns guide actin network contraction.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. 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

9 authors.

Alexandra ColinCytoMorpho Lab, Laboratoire de Physiologie Cellulaire & Végétale, Interdisciplinary Research Institute of Grenoble, University of Grenoble-Alpes, CEA, CNRS, INRA, Grenoble, France.ORCID 0000-0002-9144-3282
Tommi KotilaInstitute of Biotechnology and Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.ORCID 0000-0002-9046-5834
Christophe GuérinCytoMorpho Lab, Laboratoire de Physiologie Cellulaire & Végétale, Interdisciplinary Research Institute of Grenoble, University of Grenoble-Alpes, CEA, CNRS, INRA, Grenoble, France.
Magali Orhant-PriouxCytoMorpho Lab, Laboratoire de Physiologie Cellulaire & Végétale, Interdisciplinary Research Institute of Grenoble, University of Grenoble-Alpes, CEA, CNRS, INRA, Grenoble, France.
Benoit VianayCytoMorpho Lab, Institut de Recherche Saint Louis, U976 Human Immunology Pathophysiology Immunotherapy (HIPI), University of Paris, INSERM, CEA, Paris, France.
Alex MogilnerCourant Institute of Mathematical Sciences, New York University, New York, NY, USA.
Pekka LappalainenInstitute of Biotechnology and Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.
Manuel ThéryCytoMorpho Lab, Laboratoire de Physiologie Cellulaire & Végétale, Interdisciplinary Research Institute of Grenoble, University of Grenoble-Alpes, CEA, CNRS, INRA, Grenoble, France.ORCID 0000-0002-9968-1779
Laurent BlanchoinCytoMorpho Lab, Laboratoire de Physiologie Cellulaire & Végétale, Interdisciplinary Research Institute of Grenoble, University of Grenoble-Alpes, CEA, CNRS, INRA, Grenoble, France.ORCID 0000-0001-8146-9254

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intracellular organization is largely mediated by actin turnover. Cellular actin networks continuously assemble and disassemble, while maintaining their overall appearance. This behavior, called "dynamic steady state," allows cells to sense and adapt to their environment. However, how structural stability can be maintained during the constant turnover of a limited actin monomer pool is poorly understood. To answer this question, we developed an experimental system where polystyrene beads are propelled by an actin comet in a microwell containing a limited amount of components. We used the speed and the size of the actin comet tails to evaluate the system's monomer consumption and its lifetime. We established the relative contribution of actin assembly, disassembly, and recycling for a bead movement over tens of hours. Recycling mediated by cyclase-associated protein (CAP) is the key step in allowing the reuse of monomers for multiple assembly cycles. ATP supply and protein aging are also factors that limit the lifetime of actin turnover. This work reveals the balancing mechanism for long-term network assembly with a limited amount of building blocks.

Indexed as

Actin CytoskeletonActinsActinsactin turnoveraginglifetimemicrowellsreconstituted system

Identifiers

PMID36912152
PMCPMC10152149

What Socratic holds

Textmetadata
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 Socratic graph.