Evidence map›Paper›PMID 23916785›Full record

ReviewThe international journal of biochemistry & cell biology2013

Arg kinase signaling in dendrite and synapse stabilization pathways: memory, cocaine sensitivity, and stress.

Meghan E Kerrisk, Anthony J Koleske

Open access · greenAbstract readReview
In one paragraph

Review in The international journal of biochemistry & cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. CeOCellular and molecular neurobiology · 2019
    Article
  9. β1-Integrins in the Developing Orbitofrontal Cortex Are Necessary for Expectancy Updating in Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  10. Article
  11. Article
  12. Review
  13. 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

2 authors at 1 institution in 1 country.

Meghan E KerriskDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520, USA. Electronic address: meghan.kerrisk@yale.edu.
Anthony J Koleske
Yale University · US

Funding

Skill Development for Diverse Scientific Careers: A New Course Predoctoral Program in Cellular and Molecular BiologyT32GM007223 · NIGMS · YALE UNIVERSITY · PI BASERGA, SUSAN J · 1985 to 2019
$31.0M
Roles of Abl and Arg Neuronal DevelopmentR01NS039475 · NINDS · YALE UNIVERSITY · PI KOLESKE, ANTHONY J · 2000 to 2012
$4.3M
The mechanism of Arg kinase activation by integrin B1R01GM100411 · NIGMS · YALE UNIVERSITY · PI BOGGON, TITUS JONATHON, KOLESKE, ANTHONY J · 2012 to 2015
$1.3M
Biochemical screen--regulators of neuronal morphogenesisR21MH077306 · NIMH · YALE UNIVERSITY · PI KOLESKE, ANTHONY J · 2006 to 2007
$398k
NIGMS NIH HHS R01 GM100411NIGMS NIH HHS T32 GM007223NIMH NIH HHS R21 MH077306NINDS NIH HHS R01 NS039475
6 · The paper itself

Abstract

The Abl2/Arg nonreceptor tyrosine kinase is enriched in dendritic spines where it is essential for maintaining dendrite and synapse stability in the postnatal mouse brain. Arg is activated downstream of integrin α3β1 receptors and it regulates the neuronal actin cytoskeleton by directly binding F-actin and via phosphorylation of substrates including p190RhoGAP and cortactin. Neurons in mice lacking Arg or integrin α3β1 develop normally through postnatal day 21 (P21), however by P42 mice exhibit major reductions in dendrite arbor size and complexity, and lose dendritic spines and synapses. As a result, mice with loss of Arg and Arg-dependent signaling pathways have impairments in memory tasks, heightened sensitivity to cocaine, and vulnerability to corticosteroid-induced neuronal remodeling. Therefore, understanding the molecular mechanisms of Arg regulation may lead to therapeutic approaches to treat human psychiatric and neurodegenerative diseases in which neuronal structure is destabilized.

Indexed as

MemorySignal TransductionAnimalsCocaineDendritesHumansProtein-Tyrosine KinasesStress, PsychologicalSynapsesARG tyrosine kinaseCocaineProtein-Tyrosine KinasesAbl-related geneActin cytoskeletonArgargKDarg knockdownCa(2+)-dependent phospholipid binding domainCaLBCocaineCorticosteroidECMextracellular matrixF-actinfilamentous actinIntegrin α3β1mEPSCminiature evoked postsynaptic currentNeuronal stabilityNMDAN-methyl-d-aspartate receptorNTAN-terminal acidic domainp120p120RasGAP, 120kDa GTPase activating protein for Rasp190p190RhoGAP, 190kDa GTPase activating protein for RhoP21, P42PHpleckstrin homology domainpostnatal day 21, 42SH2, SH3Src homology domain 1,2

Identifiers

PMID23916785
PMCPMC3797846
OpenAlexW1964450959

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.