Evidence map›Paper›PMID 36662867›Full record

ArticleScience advances2023

ArpC5 isoforms regulate Arp2/3 complex-dependent protrusion through differential Ena/VASP positioning.

Florian Fäßler, Manjunath G Javoor, Julia Datler, Hermann Döring, Florian W Hofer, Georgi Dimchev, Victor-Valentin Hodirnau, Jan Faix, Klemens Rottner, Florian K M Schur

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.4field-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

19 citing papers in PubMed, 26 citations in OpenAlex.

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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

10 authors at 3 institutions in 2 countries.

Florian FäßlerInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.ORCID 0000-0001-7149-769X
Manjunath G JavoorInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Julia DatlerInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
Hermann DöringZoological Institute, Technische Universität Braunschweig, Braunschweig, Germany.ORCID 0000-0001-6699-8393
Florian W HoferInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.ORCID 0000-0002-6531-3820
Georgi DimchevInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.ORCID 0000-0001-8370-6161
Victor-Valentin HodirnauInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.ORCID 0000-0003-3904-947X
Jan FaixInstitute for Biophysical Chemistry, Hannover Medical School, Hannover, Germany.
Klemens RottnerZoological Institute, Technische Universität Braunschweig, Braunschweig, Germany.ORCID 0000-0003-4244-4198
Florian K M SchurInstitute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.ORCID 0000-0003-4790-8078
Institute of Science and Technology Austria · ATHelmholtz Centre for Infection Research · DEMedizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulation of the Arp2/3 complex is required for productive nucleation of branched actin networks. An emerging aspect of regulation is the incorporation of subunit isoforms into the Arp2/3 complex. Specifically, both ArpC5 subunit isoforms, ArpC5 and ArpC5L, have been reported to fine-tune nucleation activity and branch junction stability. We have combined reverse genetics and cellular structural biology to describe how ArpC5 and ArpC5L differentially affect cell migration. Both define the structural stability of ArpC1 in branch junctions and, in turn, by determining protrusion characteristics, affect protein dynamics and actin network ultrastructure. ArpC5 isoforms also affect the positioning of members of the Ena/Vasodilator-stimulated phosphoprotein (VASP) family of actin filament elongators, which mediate ArpC5 isoform-specific effects on the actin assembly level. Our results suggest that ArpC5 and Ena/VASP proteins are part of a signaling pathway enhancing cell migration.

Indexed as

Actin-Related Protein 2-3 ComplexActinsActin CytoskeletonMicrofilament ProteinsProtein IsoformsVasodilator-Stimulated PhosphoproteinActin-Related Protein 2-3 ComplexActinsMicrofilament ProteinsProtein IsoformsVasodilator-Stimulated Phosphoprotein

Identifiers

PMID36662867
PMCPMC9858492
OpenAlexW4317556195

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.