Evidence map›Paper›PMID 36598940›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Ena/VASP clustering at microspike tips involves lamellipodin but not I-BAR proteins, and absolutely requires unconventional myosin-X.

Thomas Pokrant, Jens Ingo Hein, Sarah Körber, Andrea Disanza, Andreas Pich, Giorgio Scita, Klemens Rottner, Jan Faix

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.0field-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

16 citing papers in PubMed, 25 citations in OpenAlex.

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  9. Liquid-like condensates mediate competition between actin branching and bundling.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. The dysadherin/FAK axis promotes individual cell migration in colon cancer.International journal of biological sciences · 2024
    Article
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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

8 authors at 4 institutions in 2 countries.

Thomas PokrantInstitute for Biophysical Chemistry, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0002-7222-8085
Jens Ingo HeinInstitute for Biophysical Chemistry, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0002-1018-7679
Sarah KörberInstitute for Biophysical Chemistry, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0002-5077-9345
Andrea DisanzaIFOM ETS (Istituto Fondazione di Oncologia Molecolare ETS),  - The AIRC (Italian Association for Cancer Research) Institute of Molecular Oncology, 20139 Milan, Italy.
Andreas PichResearch Core Unit Proteomics, Hannover Medical School, 30625 Hannover, Germany.
Giorgio ScitaIFOM ETS (Istituto Fondazione di Oncologia Molecolare ETS),  - The AIRC (Italian Association for Cancer Research) Institute of Molecular Oncology, 20139 Milan, Italy.ORCID 0000-0001-7984-1889
Klemens RottnerDivision of Molecular Cell Biology, Zoological Institute, Technische Universität Braunschweig, 38106 Braunschweig, Germany.ORCID 0000-0003-4244-4198
Jan FaixInstitute for Biophysical Chemistry, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0003-1803-9192
Medizinische Hochschule Hannover · DEHelmholtz Centre for Infection Research · DEIFOM · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sheet-like membrane protrusions at the leading edge, termed lamellipodia, drive 2D-cell migration using active actin polymerization. Microspikes comprise actin-filament bundles embedded within lamellipodia, but the molecular mechanisms driving their formation and their potential functional relevance have remained elusive. Microspike formation requires the specific activity of clustered Ena/VASP proteins at their tips to enable processive actin assembly in the presence of capping protein, but the factors and mechanisms mediating Ena/VASP clustering are poorly understood. Systematic analyses of B16-F1 melanoma mutants lacking potential candidate proteins revealed that neither inverse BAR-domain proteins, nor lamellipodin or Abi is essential for clustering, although they differentially contribute to lamellipodial VASP accumulation. In contrast, unconventional myosin-X (MyoX) identified here as proximal to VASP was obligatory for Ena/VASP clustering and microspike formation. Interestingly, and despite the invariable distribution of other relevant marker proteins, the width of lamellipodia in MyoX-KO mutants was significantly reduced as compared with B16-F1 control, suggesting that microspikes contribute to lamellipodium stability. Consistently, MyoX removal caused marked defects in protrusion and random 2D-cell migration. Strikingly, Ena/VASP-deficiency also uncoupled MyoX cluster dynamics from actin assembly in lamellipodia, establishing their tight functional association in microspike formation.

Indexed as

ActinsSynapsinsAnimalsCell Line, TumorCell MovementDNA-Binding ProteinsMiceMyosinsPhosphoproteinsPseudopodiaActinsDNA-Binding ProteinsENA-VASP proteinsMyosinsPhosphoproteinsSynapsinsI-BAR proteinslamellipodinmicrospikesmyosin-XVASP clustering

Identifiers

PMID36598940
PMCPMC9926217
OpenAlexW4313493346

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.