Evidence map›Paper›PMID 38323924›Full record

ArticleJournal of cell science2024

Filopodial protrusion driven by density-dependent Ena-TOCA-1 interactions.

Thomas C A Blake, Helen M Fox, Vasja Urbančič, Roshan Ravishankar, Adam Wolowczyk, Edward S Allgeyer, Julia Mason, Gaudenz Danuser, Jennifer L Gallop

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. The actin assembly regulatorbioRxiv : the preprint server for biology · 2025
    Article
  3. Article
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

9 authors at 2 institutions in 2 countries.

Thomas C A BlakeWellcome/Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge CB2 1QN, UK.ORCID 0000-0002-8534-0025
Helen M FoxWellcome/Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge CB2 1QN, UK.ORCID 0000-0002-6907-2278
Vasja UrbančičWellcome/Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge CB2 1QN, UK.ORCID 0000-0001-8955-5923
Roshan RavishankarLyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Adam WolowczykWellcome/Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge CB2 1QN, UK.ORCID 0000-0002-6491-9978
Edward S AllgeyerWellcome/Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge CB2 1QN, UK.ORCID 0000-0002-2187-4423
Julia MasonWellcome/Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge CB2 1QN, UK.ORCID 0000-0002-7499-6707
Gaudenz DanuserLyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0001-8583-2014
Jennifer L GallopWellcome/Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge CB2 1QN, UK.ORCID 0000-0002-9978-1382
University of Cambridge · GBSouthwestern Medical Center · US

Funding

UTSW-UNC Center for Cell Signaling AnalysisRM1GM145399 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI Kevin Michael Dean, Klaus M. Hahn · 2022 to 2026
$6.2M
Cancer Research UK C6946/A14492NIGMS NIH HHS RM1 GM145399NIGMS NIH HHS RM1GM145399Wellcome TrustWellcome Trust WT095829MA
6 · The paper itself

Abstract

Filopodia are narrow actin-rich protrusions with important roles in neuronal development where membrane-binding adaptor proteins, such as I-BAR- and F-BAR-domain-containing proteins, have emerged as upstream regulators that link membrane interactions to actin regulators such as formins and proteins of the Ena/VASP family. Both the adaptors and their binding partners are part of diverse and redundant protein networks that can functionally compensate for each other. To explore the significance of the F-BAR domain-containing neuronal membrane adaptor TOCA-1 (also known as FNBP1L) in filopodia we performed a quantitative analysis of TOCA-1 and filopodial dynamics in Xenopus retinal ganglion cells, where Ena/VASP proteins have a native role in filopodial extension. Increasing the density of TOCA-1 enhances Ena/VASP protein binding in vitro, and an accumulation of TOCA-1, as well as its coincidence with Ena, correlates with filopodial protrusion in vivo. Two-colour single-molecule localisation microscopy of TOCA-1 and Ena supports their nanoscale association. TOCA-1 clusters promote filopodial protrusion and this depends on a functional TOCA-1 SH3 domain and activation of Cdc42, which we perturbed using the small-molecule inhibitor CASIN. We propose that TOCA-1 clusters act independently of membrane curvature to recruit and promote Ena activity for filopodial protrusion.

Indexed as

ActinsPseudopodiaCarrier ProteinsForminsNeuronsActinsCarrier ProteinsForminsActinGrowth coneMigration

Identifiers

PMID38323924
PMCPMC11006392
OpenAlexW4391598748

What Socratic 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 Socratic graph.