Evidence map›Paper›PMID 26453304›Full record

ReviewThe Journal of biological chemistry2015

Actin Out: Regulation of the Synaptic Cytoskeleton.

Erin F Spence, Scott H Soderling

Open access · hybridAbstract readReview
In one paragraph

Review in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

107 citing papers in PubMed, 180 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Cofilin Inhibition Ameliorates PIEZO2 and AMPA Dysfunction in a Mouse Model of Angelman Syndrome.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Microglia Support Both the Singular Form of LTP Expressed by the Lateral Perforant Path and Episodic Memory.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Cell Adhesion Molecule Signaling at the Synapse: Beyond the Scaffold.Cold Spring Harbor perspectives in biology · 2024
    Review
  20. Presynaptic Rac1 in the hippocampus selectively regulates working memory.bioRxiv : the preprint server for biology · 2024
    Article

47 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

2 authors at 1 institution in 2 countries.

Erin F SpenceFrom the Departments of Cell Biology and.
Scott H SoderlingFrom the Departments of Cell Biology and Neurobiology, Duke University, School of Medicine, Durham, North Carolina 27710 scott.soderling@duke.edu.
Duke University · US

Funding

ORGANIZATION AND FUNCTIONS OF CELLULAR STRUCTUREST32GM007184 · NIGMS · DUKE UNIVERSITY · PI JINKS-ROBERTSON, SUE · 1985 to 2019
$18.2M
GAPs in Signaling to the Spine and Retardation: Mechanisms and the Role of WRPR01NS059957 · NINDS · DUKE UNIVERSITY · PI SODERLING, SCOTT H · 2008 to 2017
$3.1M
Molecular, Synaptic, and Circuit Basis for Schizophrenia-related PhenotypesR01MH103374 · NIMH · DUKE UNIVERSITY · PI SODERLING, SCOTT H · 2014 to 2018
$2.0M
Fragile X Phenotypes Modulated by Altered Signaling to the Synaptic CytoskeletonR56NS059957 · NINDS · DUKE UNIVERSITY · PI SODERLING, SCOTT H · 2013 to 2013
$393k
Analysis of Arp2/3 activity as a major driver of dendritic spinogenesisF31NS092402 · NINDS · DUKE UNIVERSITY · PI SPENCE, ERIN FAITH · 2015 to 2018
$97k
NIGMS NIH HHS T32 GM007184NIMH NIH HHS MH103374NIMH NIH HHS R01 MH103374NINDS NIH HHS F31 NS092402NINDS NIH HHS NS059957NINDS NIH HHS R01 NS059957NINDS NIH HHS R56 NS059957
6 · The paper itself

Abstract

The small size of dendritic spines belies the elaborate role they play in excitatory synaptic transmission and ultimately complex behaviors. The cytoskeletal architecture of the spine is predominately composed of actin filaments. These filaments, which at first glance might appear simple, are also surprisingly complex. They dynamically assemble into different structures and serve as a platform for orchestrating the elaborate responses of the spine during spinogenesis and experience-dependent plasticity. Multiple mutations associated with human neurodevelopmental and psychiatric disorders involve genes that encode regulators of the synaptic cytoskeleton. A major, unresolved question is how the disruption of specific actin filament structures leads to the onset and progression of complex synaptic and behavioral phenotypes. This review will cover established and emerging mechanisms of actin cytoskeletal remodeling and how this influences specific aspects of spine biology that are implicated in disease.

Indexed as

ActinsAnimalsHumansSpinal DiseasesSpineStress FibersSynapsesActinsactinadhesionArp2/3 complexcofilindendritic spineforminRho (Rho GTPase)synapsesynaptic plasticityWASH

Identifiers

PMID26453304
PMCPMC4661376
OpenAlexW2178224525

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.