Evidence map›Paper›PMID 26038554›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Two-tiered coupling between flowing actin and immobilized N-cadherin/catenin complexes in neuronal growth cones.

Mikael Garcia, Cécile Leduc, Matthieu Lagardère, Amélie Argento, Jean-Baptiste Sibarita, Olivier Thoumine

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Forces to Drive Neuronal Migration Steps.Frontiers in cell and developmental biology · 2020
    Review
  13. Article
  14. Using Single-Protein Tracking to Study Cell Migration.Methods in molecular biology (Clifton, N.J.) · 2018
    Article
  15. Article
  16. Defective Gpsm2/GαNature communications · 2017
    Article
  17. Article
  18. Gene silencing NMII promotes axonal regeneration against contusive spinal cord injury in rats.International journal of clinical and experimental pathology · 2017
    Article
  19. Article
  20. 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 1 country.

Mikael GarciaInterdisciplinary Institute for Neuroscience, UMR 5297, Centre National de la Recherche Scientifique (CNRS), University of Bordeaux, 33077 Bordeaux, France; CYTOO SA, Minatec, 38040 Grenoble, France;
Cécile LeducCell Polarity, Migration, and Cancer Unit, CNRS, Unité de Recherche Associée 2582, Institut Pasteur, 75724 Paris Cedex 15, France.
Matthieu LagardèreInterdisciplinary Institute for Neuroscience, UMR 5297, Centre National de la Recherche Scientifique (CNRS), University of Bordeaux, 33077 Bordeaux, France;
Amélie ArgentoCYTOO SA, Minatec, 38040 Grenoble, France;
Jean-Baptiste SibaritaInterdisciplinary Institute for Neuroscience, UMR 5297, Centre National de la Recherche Scientifique (CNRS), University of Bordeaux, 33077 Bordeaux, France;
Olivier ThoumineInterdisciplinary Institute for Neuroscience, UMR 5297, Centre National de la Recherche Scientifique (CNRS), University of Bordeaux, 33077 Bordeaux, France; olivier.thoumine@u-bordeaux.fr.
Centre National de la Recherche Scientifique · FRInstitut polytechnique de Grenoble · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuronal growth cones move forward by dynamically connecting actin-based motility to substrate adhesion, but the mechanisms at the individual molecular level remain unclear. We cultured primary neurons on N-cadherin-coated micropatterned substrates, and imaged adhesion and cytoskeletal proteins at the ventral surface of growth cones using single particle tracking combined to photoactivated localization microscopy (sptPALM). We demonstrate transient interactions in the second time scale between flowing actin filaments and immobilized N-cadherin/catenin complexes, translating into a local reduction of the actin retrograde flow. Normal actin flow on micropatterns was rescued by expression of a dominant negative N-cadherin construct competing for the coupling between actin and endogenous N-cadherin. Fluorescence recovery after photobleaching (FRAP) experiments confirmed the differential kinetics of actin and N-cadherin, and further revealed a 20% actin population confined at N-cadherin micropatterns, contributing to local actin accumulation. Computer simulations with relevant kinetic parameters modeled N-cadherin and actin turnover well, validating this mechanism. Such a combination of short- and long-lived interactions between the motile actin network and spatially restricted adhesive complexes represents a two-tiered clutch mechanism likely to sustain dynamic environment sensing and provide the force necessary for growth cone migration.

Indexed as

ActinsAnimalsBiomechanical PhenomenaCadherinsCateninsCell MovementDNA PrimersEmbryo, MammalianFluorescenceFluorescence Recovery After PhotobleachingGrowth ConesHippocampusImmunohistochemistryMolecular Dynamics SimulationMultiprotein ComplexesPolymerase Chain ReactionActinsCadherinsCateninsDNA PrimersMultiprotein Complexesactin flowgrowth conemicropatterned substratesN-cadherin adhesionsingle-molecule tracking

Identifiers

PMID26038554
PMCPMC4460488
OpenAlexW1959419435

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.