Evidence map›Paper›PMID 15128850›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2004

p75 neurotrophin receptor signaling regulates growth cone filopodial dynamics through modulating RhoA activity.

Scott Gehler, Gianluca Gallo, Eric Veien, Paul C Letourneau

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

64 citing papers in PubMed, 131 citations in OpenAlex.

  1. Article
  2. AraC interacts with p75Cell death & disease · 2023
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. The Slow-Releasing and Mitochondria-Targeted Hydrogen Sulfide (HInternational journal of molecular sciences · 2021
    Article
  9. Article
  10. p75NTR and DR6 Regulate Distinct Phases of Axon Degeneration Demarcated by Spheroid Rupture.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  11. Swedish Nerve Growth Factor Mutation (NGFThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Guidance of Axons by Local Coupling of Retrograde Flow to Point Contact Adhesions.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  19. Article
  20. Review

4 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Scott GehlerDepartment of Neuroscience, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Gianluca Gallo
Eric Veien
Paul C Letourneau
University of Minnesota · USDrexel University · 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
NICHD NIH HHS HD19950NICHD NIH HHS R01 HD019950
6 · The paper itself

Abstract

The mechanisms by which neurotrophins regulate growth cone motility are unclear. We investigated the role of the p75 neurotrophin receptor (p75NTR) in mediating neurotrophin-induced increases in filopodial length. Our data demonstrate that neurotrophin binding to p75NTR is necessary and sufficient to regulate filopodial dynamics. Furthermore, retinal and dorsal root ganglion growth cones from p75 mutant mice are insensitive to neurotrophins but display enhanced filopodial lengths comparable with neurotrophin-treated wild-type growth cones. This suggests unoccupied p75NTR negatively regulates filopodia length. Furthermore, p75NTR regulates RhoA activity to mediate filopodial dynamics. Constitutively active RhoA blocks neurotrophin-induced increases in filopodial length, whereas inhibition of RhoA enhances filopodial lengths, similar to neurotrophin treatment. BDNF treatment of retinal neurons results in reduced RhoA activity. Furthermore, p75 mutant neurons display reduced levels of activated RhoA compared with wild-type counterparts, consistent with the enhanced filopodial lengths observed on mutant growth cones. These observations suggest that neurotrophins regulate filopodial dynamics by depressing the activation of RhoA that occurs through p75NTR signaling.

Indexed as

AnimalsBrain-Derived Neurotrophic FactorChick EmbryoDose-Response Relationship, DrugEnzyme ActivationEnzyme InhibitorsGanglia, SpinalGrowth ConesMiceMice, Mutant StrainsNerve Growth FactorsNeuronsPseudopodiaReceptor, Nerve Growth FactorReceptors, Nerve Growth FactorRetinaBrain-Derived Neurotrophic FactorEnzyme InhibitorsNerve Growth FactorsReceptor, Nerve Growth FactorReceptors, Nerve Growth FactorrhoA GTP-Binding Protein

Identifiers

PMID15128850
PMCPMC6729430
OpenAlexW2080347303

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.