Evidence map›Paper›PMID 29851558›Full record

ArticleMolecular biology of the cell2018

The contributions of the actin machinery to endocytic membrane bending and vesicle formation.

Andrea Picco, Wanda Kukulski, Hetty E Manenschijn, Tanja Specht, John A G Briggs, Marko Kaksonen

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

35 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Cardiolipin membranes drive Myosin VI activation, oligomerization, and processive cargo transport.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. A role for cross-linking proteins in actin filament network organization and force generation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Regulation of membrane scission in yeast endocytosis.Molecular biology of the cell · 2022
    Article
  15. Article
  16. Programmable DNA-augmented hydrogels for controlled activation of human lymphocytes.Nanomedicine : nanotechnology, biology, and medicine · 2021
    Article
  17. Article
  18. Article
  19. Biophysical forces in membrane bending and traffic.Current opinion in cell biology · 2020
    Review
  20. Lung Endothelial Transcytosis.Comprehensive Physiology · 2020
    Review
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 at 2 institutions in 3 countries.

Andrea PiccoDepartment of Biochemistry and NCCR Chemical Biology, University of Geneva, 1211 Geneva, Switzerland.
Wanda KukulskiCell Biology and Biophysics Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
Hetty E ManenschijnDepartment of Biochemistry and NCCR Chemical Biology, University of Geneva, 1211 Geneva, Switzerland.
Tanja SpechtCell Biology and Biophysics Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
John A G BriggsCell Biology and Biophysics Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
Marko KaksonenDepartment of Biochemistry and NCCR Chemical Biology, University of Geneva, 1211 Geneva, Switzerland.
European Molecular Biology Laboratory · DENCCR Chemical Biology - Visualisation and Control of Biological Processes Using Chemistry · CH

Funding

Medical Research Council MC_UP_1201/16Medical Research Council MC_UP_1201/8
6 · The paper itself

Abstract

Branched and cross-linked actin networks mediate cellular processes that move and shape membranes. To understand how actin contributes during the different stages of endocytic membrane reshaping, we analyzed deletion mutants of yeast actin network components using a hybrid imaging approach that combines live imaging with correlative microscopy. We could thus temporally dissect the effects of different actin network perturbations, revealing distinct stages of actin-based membrane reshaping. Our data show that initiation of membrane bending requires the actin network to be physically linked to the plasma membrane and to be optimally cross-linked. Once initiated, the membrane invagination process is driven by nucleation and polymerization of new actin filaments, independent of the degree of cross-linking and unaffected by a surplus of actin network components. A key transition occurs 2 s before scission, when the filament nucleation rate drops. From that time point on, invagination growth and vesicle scission are driven by an expansion of the actin network without a proportional increase of net actin amounts. The expansion is sensitive to the amount of filamentous actin and its cross-linking. Our results suggest that the mechanism by which actin reshapes the membrane changes during the progress of endocytosis, possibly adapting to varying force requirements.

Indexed as

EndocytosisActin CytoskeletonActinsCell MembraneClathrinMutationSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSecretory VesiclesActinsClathrinSaccharomyces cerevisiae Proteins

Identifiers

PMID29851558
PMCPMC5994895
OpenAlexW2950237256

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.