Evidence map›Paper›PMID 23173822›Full record

ArticleJournal of neurochemistry2013

Differential association of postsynaptic signaling protein complexes in striatum and hippocampus.

Anthony J Baucum, Abigail M Brown, Roger J Colbran

Abstract read
In one paragraph

Article in Journal of neurochemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

  1. Mechanisms of spinophilin-dependent pancreas dysregulation in obesity.American journal of physiology. Endocrinology and metabolism · 2024
    Article
  2. Review
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  6. Regulation of Synaptic Transmission and Plasticity by Protein Phosphatase 1.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Review
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  14. A Novel HumanThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
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  20. In vivo amphetamine action is contingent on αCaMKII.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2014
    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

3 authors at 2 institutions in 1 country.

Anthony J BaucumDepartment of Molecular Physiology and Biophysics, Vanderbilt Kennedy Center, Vanderbilt University School of Medicine, Nashville, Tennessee, USA. anthony.baucum@vanderbilt.edu
Abigail M Brown
Roger J Colbran
John F. Kennedy Center for the Performing Arts · USVanderbilt University · US

Funding

Program in NeurogenomicsT32MH065215 · NIMH · VANDERBILT UNIVERSITY · PI ROGER J COLBRAN · 2002 to 2026
$6.4M
Mechanisms of CaM Kinase II Signal TransductionR01MH063232 · NIMH · VANDERBILT UNIVERSITY · PI COLBRAN, ROGER J · 2001 to 2015
$5.4M
Spinophilin Signaling in the StriatumK01NS073700 · NINDS · VANDERBILT UNIVERSITY · PI BAUCUM, ANTHONY J. · 2012 to 2016
$693k
NIMH NIH HHS R01 MH063232NIMH NIH HHS R01-MH063232NIMH NIH HHS T32 MH065215NINDS NIH HHS K01 NS073700NINDS NIH HHS K01NS073700
6 · The paper itself

Abstract

Distinct physiological stimuli are required for bidirectional synaptic plasticity in striatum and hippocampus, but differences in the underlying signaling mechanisms are poorly understood. We have begun to compare levels and interactions of key excitatory synaptic proteins in whole extracts and subcellular fractions isolated from micro-dissected striatum and hippocampus. Levels of multiple glutamate receptor subunits, calcium/calmodulin-dependent protein kinase II (CaMKII), a highly abundant serine/threonine kinase, and spinophilin, a F-actin and protein phosphatase 1 (PP1) binding protein, were significantly lower in striatal extracts, as well as in synaptic and/or extrasynaptic fractions, compared with similar hippocampal extracts/fractions. However, CaMKII interactions with spinophilin were more robust in striatum compared with hippocampus, and this enhanced association was restricted to the extrasynaptic fraction. NMDAR GluN2B subunits associate with both spinophilin and CaMKII, but spinophilin-GluN2B complexes were enriched in extrasynaptic fractions whereas CaMKII-GluN2B complexes were enriched in synaptic fractions. Notably, the association of GluN2B with both CaMKII and spinophilin was more robust in striatal extrasynaptic fractions compared with hippocampal extrasynaptic fractions. Selective differences in the assembly of synaptic and extrasynaptic signaling complexes may contribute to differential physiological regulation of excitatory transmission in striatum and hippocampus.

Indexed as

AnimalsCalcium-Calmodulin-Dependent Protein Kinase Type 2Corpus StriatumHippocampusImmunoprecipitationMaleMiceMice, Inbred C57BLMicrofilament ProteinsMyosinsNerve Tissue ProteinsNeurabinsPhosphorylationProtein Phosphatase 1Receptors, GlutamateReceptors, N-Methyl-D-AspartateCalcium-Calmodulin-Dependent Protein Kinase Type 2Microfilament ProteinsMyosinsNerve Tissue ProteinsNeurabinsNR2B NMDA receptorpostsynaptic density proteinsProtein Phosphatase 1Receptors, GlutamateReceptors, N-Methyl-D-AspartateVesicular Transport Proteins

Identifiers

PMID23173822
PMCPMC3557548
OpenAlexW2091368956

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.