Evidence map›Paper›PMID 36253374›Full record

ArticleNature communications2022

Actin polymerization promotes invagination of flat clathrin-coated lattices in mammalian cells by pushing at lattice edges.

Changsong Yang, Patricia Colosi, Siewert Hugelier, Daniel Zabezhinsky, Melike Lakadamyali, Tatyana Svitkina

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. 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
3.6field-weighted citation impact, top 6% 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

15 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Organelle contact sites in cancer cells.Cell death & disease · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Polymerization force-regulated actin filament-Arp2/3 complex interaction dominates self-adaptive cell migrations.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  14. Article
  15. Exosomal transmission of viruses, a two-edged biological sword.Cell communication and signaling : CCS · 2023
    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 1 institution in 1 country.

Changsong YangDepartment of Biology, University of Pennsylvania, Philadelphia, PA, USA.
Patricia ColosiDepartment of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Siewert HugelierDepartment of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0002-6224-652X
Daniel ZabezhinskyDepartment of Biology, University of Pennsylvania, Philadelphia, PA, USA.
Melike LakadamyaliDepartment of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0002-7524-6414
Tatyana SvitkinaDepartment of Biology, University of Pennsylvania, Philadelphia, PA, USA. svitkina@sas.upenn.edu.ORCID 0000-0002-8424-447X
University of Pennsylvania · US

Funding

Structure and functions of the actin cytoskeletonR35GM140832 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI Tatyana Svitkina · 2021 to 2026
$2.8M
Calibration nanotemplates as universal standards for determining protein copy number in super-resolution microscopyR01GM133842 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI LAKADAMYALI, MELIKE · 2019 to 2022
$1.7M
NIGMS NIH HHS R01 GM133842NIGMS NIH HHS R35 GM140832
6 · The paper itself

Abstract

Clathrin-mediated endocytosis (CME) requires energy input from actin polymerization in mechanically challenging conditions. The roles of actin in CME are poorly understood due to inadequate knowledge of actin organization at clathrin-coated structures (CCSs). Using platinum replica electron microscopy of mammalian cells, we show that Arp2/3 complex-dependent branched actin networks, which often emerge from microtubule tips, assemble along the CCS perimeter, lack interaction with the apical clathrin lattice, and have barbed ends oriented toward the CCS. This structure is hardly compatible with the widely held "apical pulling" model describing actin functions in CME. Arp2/3 complex inhibition or epsin knockout produce large flat non-dynamic CCSs, which split into invaginating subdomains upon recovery from Arp2/3 inhibition. Moreover, epsin localization to CCSs depends on Arp2/3 activity. We propose an "edge pushing" model for CME, wherein branched actin polymerization promotes severing and invagination of flat CCSs in an epsin-dependent manner by pushing at the CCS boundary, thus releasing forces opposing the intrinsic curvature of clathrin lattices.

Indexed as

ActinsPlatinumActin-Related Protein 2-3 ComplexAnimalsClathrinClathrin-Coated VesiclesEndocytosisMammalsPolymerizationActin-Related Protein 2-3 ComplexActinsClathrinPlatinum

Identifiers

PMID36253374
PMCPMC9576739
OpenAlexW4306406740

What OpenQuestion holds

Textmetadata
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.