Evidence map›Paper›PMID 38968072›Full record

ArticleCell reports2024

Competition and synergy of Arp2/3 and formins in nucleating actin waves.

Xiang Le Chua, Chee San Tong, Maohan Su, X J Xǔ, Shengping Xiao, Xudong Wu, Min Wu

Abstract read
In one paragraph

Article in Cell reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Mitotic Cdc42 waves encode PI(3,4)PScience advances · 2026
    Article
  2. Article
  3. Distinct impact of PI(4)P flux on PI(4,5)PProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Article
  5. Article
  6. Signaling and actin waves at a glance.Journal of cell science · 2025
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. The role of actin cytoskeleton component Arp2/3 in inflammatory response.Frontiers in cell and developmental biology · 2025
    Review
  12. Nonlinear dynamics in phosphoinositide metabolism.Current opinion in cell biology · 2024
    Review
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Xiang Le ChuaDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT 06510, USA; Department of Biological Sciences, Centre for Bioimaging Sciences, Singapore 117557, Singapore.
Chee San TongDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT 06510, USA; Department of Biological Sciences, Centre for Bioimaging Sciences, Singapore 117557, Singapore.
Maohan SuDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT 06510, USA; Department of Biological Sciences, Centre for Bioimaging Sciences, Singapore 117557, Singapore; Mechanobiology Institute, National University of Singapore, Singapore 117411, Singapore.
X J XǔDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT 06510, USA; Department of Physics, Yale University, New Haven, CT 06511, USA.
Shengping XiaoDepartment of Biological Sciences, Centre for Bioimaging Sciences, Singapore 117557, Singapore.
Xudong WuSchool of Life Sciences, Westlake University, Hangzhou 310024, China.
Min WuDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT 06510, USA; Department of Biological Sciences, Centre for Bioimaging Sciences, Singapore 117557, Singapore; Mechanobiology Institute, National University of Singapore, Singapore 117411, Singapore. Electronic address: wu.min@yale.edu.

Funding

Endocytic dynamics and surface emergent property of leukocyte IntegrinsR01GM151344 · NIGMS · YALE UNIVERSITY · PI Min Wu · 2023 to 2026
$1.9M
NIGMS NIH HHS R01 GM151344
6 · The paper itself

Abstract

Actin assembly and dynamics are crucial for maintaining cell structure and changing physiological states. The broad impact of actin on various cellular processes makes it challenging to dissect the specific role of actin regulatory proteins. Using actin waves that propagate on the cortex of mast cells as a model, we discovered that formins (FMNL1 and mDia3) are recruited before the Arp2/3 complex in actin waves. GTPase Cdc42 interactions drive FMNL1 oscillations, with active Cdc42 and the constitutively active mutant of FMNL1 capable of forming waves on the plasma membrane independently of actin waves. Additionally, the delayed recruitment of Arp2/3 antagonizes FMNL1 and active Cdc42. This antagonism is not due to competition for monomeric actin but rather for their common upstream regulator, active Cdc42, whose levels are negatively regulated by Arp2/3 via SHIP1 recruitment. Collectively, our study highlights the complex feedback loops in the dynamic control of the actin cytoskeletal network.

Indexed as

Actin-Related Protein 2-3 ComplexActinsForminsActin CytoskeletonAnimalscdc42 GTP-Binding ProteinHumansMast CellsMiceActin-Related Protein 2-3 ComplexActinscdc42 GTP-Binding ProteinForminsactin wavesCP: Cell biologydynamical systemslimited pool model

Identifiers

PMID38968072
PMCPMC11378572

What OpenQuestion 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 OpenQuestion graph.