Evidence map›Paper›PMID 23658184›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2013

A Myosin Va mutant mouse with disruptions in glutamate synaptic development and mature plasticity in visual cortex.

Akira Yoshii, Jian-Ping Zhao, Swarna Pandian, Brigitte van Zundert, Martha Constantine-Paton

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

23 citing papers in PubMed, 39 citations in OpenAlex.

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  4. Loss of Depalmitoylation Disrupts Homeostatic Plasticity of AMPARs in a Mouse Model of Infantile Neuronal Ceroid Lipofuscinosis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
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  15. Cdk5 Regulates Activity-Dependent Gene Expression and Dendrite Development.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
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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

5 authors at 2 institutions in 2 countries.

Akira YoshiiDepartment of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA. ayoshii@mit.edu
Jian-Ping Zhao
Swarna Pandian
Brigitte van Zundert
Martha Constantine-Paton
McGovern Institute for Brain Research · USUniversidad Andrés Bello · CL

Funding

Developmental Regulation of Glutamate Receptor FunctionR01EY014074 · NEI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI CONSTANTINE-PATON, MARTHA NA · 2003 to 2017
$5.2M
Glutamate Receptor Trafficking in Visual DevelopmentR03EY014420 · NEI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI CONSTANTINE-PATON, MARTHA · 2003 to 2005
$489k
NEI NIH HHS EY014420NEI NIH HHS R01 EY014074NEI NIH HHS R01-EY014074 -17NEI NIH HHS R03 EY014420
6 · The paper itself

Abstract

Myosin Va (MyoVa) mediates F-actin-based vesicular transport toward the plasma membrane and is found at neuronal postsynaptic densities (PSDs), but the role of MyoVa in synaptic development and function is largely unknown. Here, in studies using the dominant-negative MyoVa neurological mutant mouse Flailer, we find that MyoVa plays an essential role in activity-dependent delivery of PSD-95 and other critical PSD molecules to synapses and in endocytosis of AMPA-type glutamate receptors (AMPAR) in the dendrites of CNS neurons. MyoVa is known to carry a complex containing the major scaffolding proteins of the mature PSD, PSD-95, SAPAP1/GKAP, Shank, and Homer to dendritic spine synapses. In Flailer, neurons show abnormal dendritic shaft localization of PSD-95, stargazin, dynamin3, AMPARs and abnormal spine morphology. Flailer neurons also have abnormally high AMPAR miniature current frequencies and spontaneous AMPAR currents that are more frequent and larger than in wild-type while numbers of NMDAR containing synapses remain normal. The AMPAR abnormalities are consistent with a severely disrupted developmental regulation of long-term depression that we find in cortical Flailer neurons. Thus MyoVa plays a fundamentally important role both in localizing mature glutamate synapses to spines and in organizing the synapse for normal function. For this reason Flailer mice will be valuable in further dissecting the role of MyoVa in normal synaptic and circuit refinement and also in studies of neurological and neuropsychiatric diseases where disruptions of normal glutamate synapses are frequently observed.

Indexed as

AnimalsBiophysicsCells, CulturedDendritesDisks Large Homolog 4 ProteinElectric StimulationElectroporationEmbryo, MammalianExcitatory Amino Acid AgentsFemaleGlutamic AcidGreen Fluorescent ProteinsGuanylate KinasesImmunoprecipitationIn Vitro TechniquesMaleDisks Large Homolog 4 ProteinDlg4 protein, mouseExcitatory Amino Acid AgentsGlutamic AcidGreen Fluorescent ProteinsGuanylate KinasesMembrane ProteinsMyo5a protein, mouseMyosin Heavy ChainsMyosin Type VNerve Tissue Proteins

Identifiers

PMID23658184
PMCPMC3699337
OpenAlexW1970291634

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.