Evidence map›Paper›PMID 22219290›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

Activation of ezrin/radixin/moesin mediates attractive growth cone guidance through regulation of growth cone actin and adhesion receptors.

Bonnie M Marsick, Jose E San Miguel-Ruiz, Paul C Letourneau

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.7field-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

37 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  13. Podoplanin Gene Disruption in Mice PromotesFrontiers in cellular neuroscience · 2019
    Article
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  16. Cell Migration in 1D and 2D Nanofiber Microenvironments.Annals of biomedical engineering · 2018
    Article
  17. 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

3 authors at 2 institutions in 1 country.

Bonnie M MarsickDepartment of Neuroscience, Graduate Program in Neuroscience, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Jose E San Miguel-Ruiz
Paul C Letourneau
Twin Cities Orthopedics · USUniversity of Minnesota · US

Funding

MECHANISMS OF NERVE GROWTH CONE TURNING AND BRANCHINGR01HD019950 · NICHD · UNIVERSITY OF MINNESOTA TWIN CITIES · PI LETOURNEAU, PAUL C. · 1985 to 2013
$3.2M
VISUAL NEUROSCIENCE TRAINING PROGRAMT32EY007133 · NEI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MCLOON, STEVEN C · 1991 to 2010
$2.0M
NEI NIH HHS EY07133NEI NIH HHS T32 EY007133NICHD NIH HHS HD 19950NICHD NIH HHS R01 HD019950
6 · The paper itself

Abstract

The development of a functioning neural network relies on responses of axonal growth cones to molecular guidance cues that are encountered en route to their target tissue. Nerve growth factor (NGF) and neurotrophin-3 serve as attractive cues for chick embryo sensory growth cones in vitro and in vivo, but little is known about the actin-binding proteins necessary to mediate this response. The evolutionarily conserved ezrin/radixin/moesin (ERM) family of proteins can tether actin filaments to the cell membrane when phosphorylated at a conserved threonine residue. Here we show that acute neurotrophin stimulation rapidly increases active phospho-ERM levels in chick sensory neuron growth cone filopodia, coincident with an increase in filopodial L1 and β-integrin. Disrupting ERM function with a dominant-negative construct (DN-ERM) results in smaller and less motile growth cones with disorganized actin filaments. Previously, we found that NGF treatment increases actin-depolymerizing factor (ADF)/cofilin activity and growth cone F-actin (Marsick et al., 2010). Here, we show this F-actin increase, as well as attractive turning to NGF, is blocked when ERM function is disrupted despite normal activation of ADF/cofilin. We further show that DN-ERM expression disrupts leading edge localization of active ADF/cofilin and free F-actin barbed ends. Moreover, filopodial phospho-ERM levels are increased by incorporation of active ADF/cofilin and reduced by knockdown of L1CAM.Together, these data suggest that ERM proteins organize actin filaments in sensory neuron growth cones and are crucial for neurotrophin-induced remodeling of F-actin and redistribution of adhesion receptors.

Indexed as

ActinsAnimalsChick EmbryoChickensCytoskeletal ProteinsEzrinFemaleGanglia, SpinalGrowth ConesMaleMembrane ProteinsMicrofilament ProteinsPrimary Cell CultureSensory Receptor CellsActinsCytoskeletal ProteinsEzrinMembrane ProteinsMicrofilament Proteinsmoesinradixin

Identifiers

PMID22219290
PMCPMC3306234
OpenAlexW1997290033

What OpenQuestion holds

Textmetadata
LicenceTDM
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.