Evidence map›Paper›PMID 28185854›Full record

ArticleMolecular and cellular neurosciences2017

A dual role for the RhoGEF Ephexin5 in regulation of dendritic spine outgrowth.

A M Hamilton, J T Lambert, L K Parajuli, O Vivas, D K Park, I S Stein, J N Jahncke, M E Greenberg, S S Margolis, K Zito

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular neurosciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-weighted citation impact, top 31% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. ACS chemical neuroscience · 2026
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  5. Activity-Dependent Stabilization of Nascent Dendritic Spines Requires Nonenzymatic CaMKIIα Function.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  6. Article
  7. Review
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  14. Tiam1 is Critical for Glutamatergic Synapse Structure and Function in the Hippocampus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  15. Review
  16. Review
  17. 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

10 authors at 3 institutions in 1 country.

A M HamiltonCenter for Neuroscience, University of California Davis, Davis, CA 95618, USA.
J T LambertCenter for Neuroscience, University of California Davis, Davis, CA 95618, USA.
L K ParajuliCenter for Neuroscience, University of California Davis, Davis, CA 95618, USA.
O VivasCenter for Neuroscience, University of California Davis, Davis, CA 95618, USA.
D K ParkCenter for Neuroscience, University of California Davis, Davis, CA 95618, USA.
I S SteinCenter for Neuroscience, University of California Davis, Davis, CA 95618, USA.
J N JahnckeCenter for Neuroscience, University of California Davis, Davis, CA 95618, USA.
M E GreenbergDepartment of Neurobiology, Harvard Medical School, Boston, MA 02115, USA.
S S MargolisDepartment of Biological Chemistry, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
K ZitoCenter for Neuroscience, University of California Davis, Davis, CA 95618, USA. Electronic address: kzito@ucdavis.edu.
University of California, Davis · USHarvard University · USJohns Hopkins University · US

Funding

UC Davis MCB T32 Administrative Supplement to Recognize Excellence in Diversity, Equity, Inclusion, and Accessibility (DEIA) MentorshipT32GM007377 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI CHEDIN, FREDERIC LOUIS · 1985 to 2023
$9.9M
Mechanisms of Dendritic Spine EliminationR01NS062736 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ZITO, KAREN · 2009 to 2019
$3.8M
NIGMS NIH HHS T32 GM007377NINDS NIH HHS R01 NS062736
6 · The paper itself

Abstract

The outgrowth of new dendritic spines is closely linked to the formation of new synapses, and is thought to be a vital component of the experience-dependent circuit plasticity that supports learning. Here, we examined the role of the RhoGEF Ephexin5 in driving activity-dependent spine outgrowth. We found that reducing Ephexin5 levels increased spine outgrowth, and increasing Ephexin5 levels decreased spine outgrowth in a GEF-dependent manner, suggesting that Ephexin5 acts as an inhibitor of spine outgrowth. Notably, we found that increased neural activity led to a proteasome-dependent reduction in the levels of Ephexin5 in neuronal dendrites, which could facilitate the enhanced spine outgrowth observed following increased neural activity. Surprisingly, we also found that Ephexin5-GFP levels were elevated on the dendrite at sites of future new spines, prior to new spine outgrowth. Moreover, lowering neuronal Ephexin5 levels inhibited new spine outgrowth in response to both global increases in neural activity and local glutamatergic stimulation of the dendrite, suggesting that Ephexin5 is necessary for activity-dependent spine outgrowth. Our data support a model in which Ephexin5 serves a dual role in spinogenesis, acting both as a brake on overall spine outgrowth and as a necessary component in the site-specific formation of new spines.

Indexed as

AnimalsDendritic SpinesExcitatory Amino AcidsFemaleGlutamic AcidGreen Fluorescent ProteinsHippocampusIn Vitro TechniquesMaleMice, Inbred C57BLMice, KnockoutMicroscopy, ConfocalNeuronal PlasticityNeuronsOrgan Culture TechniquesRatsExcitatory Amino AcidsGlutamic AcidGreen Fluorescent ProteinsRho Guanine Nucleotide Exchange FactorsRNA, Small InterferingActivity-dependentDendritic spineEphexin5HippocampusProteasomeStructural plasticity

Identifiers

PMID28185854
PMCPMC5526822
OpenAlexW2587224222

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.