Evidence map›Paper›PMID 32726629›Full record

ArticleCell reports2020

Dysregulation of the Synaptic Cytoskeleton in the PFC Drives Neural Circuit Pathology, Leading to Social Dysfunction.

Il Hwan Kim, Namsoo Kim, Sunwhi Kim, Koji Toda, Christina M Catavero, Jamie L Courtland, Henry H Yin, Scott H Soderling

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 38 citations in OpenAlex.

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  15. The effect of selective nigrostriatal dopamine excess on behaviors linked to the cognitive and negative symptoms of schizophrenia.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
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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

8 authors at 2 institutions in 1 country.

Il Hwan KimDepartment of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN, USA; Department of Psychiatry and Behavioral Sciences, Duke University Medical School, Durham, NC, USA.
Namsoo KimDepartment of Psychology and Neuroscience, Duke University, Durham, NC, USA.
Sunwhi KimDepartment of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN, USA.
Koji TodaDepartment of Psychology and Neuroscience, Duke University, Durham, NC, USA.
Christina M CataveroDepartment of Cell Biology, Duke University Medical School, Durham, NC, USA.
Jamie L CourtlandDepartment of Cell Biology, Duke University Medical School, Durham, NC, USA; Department of Neurobiology, Duke University Medical School, Durham, NC, USA.
Henry H YinDepartment of Psychology and Neuroscience, Duke University, Durham, NC, USA; Department of Neurobiology, Duke University Medical School, Durham, NC, USA.
Scott H SoderlingDepartment of Cell Biology, Duke University Medical School, Durham, NC, USA; Department of Neurobiology, Duke University Medical School, Durham, NC, USA. Electronic address: scott.soderling@duke.edu.
Duke University · USUniversity of Tennessee Health Science Center · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
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
Striatal Circuits for Goal PursuitR01MH112883 · NIMH · DUKE UNIVERSITY · PI YIN, HENRY · 2017 to 2021
$1.6M
Genes, Neural Circuits, and BehaviorR01MH117429 · NIMH · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI KIM, IL HWAN · 2019 to 2022
$1.5M
Genes, Neural Circuits, and BehaviorR56MH117429 · NIMH · DUKE UNIVERSITY · PI KIM, IL HWAN · 2018 to 2018
$400k
Fragile X Phenotypes Modulated by Altered Signaling to the Synaptic CytoskeletonR56NS059957 · NINDS · DUKE UNIVERSITY · PI SODERLING, SCOTT H · 2013 to 2013
$393k
NIGMS NIH HHS T32 GM007171NIMH NIH HHS R01 MH103374NIMH NIH HHS R01 MH112883NIMH NIH HHS R01 MH117429NIMH NIH HHS R56 MH117429NINDS NIH HHS R01 NS059957NINDS NIH HHS R56 NS059957
6 · The paper itself

Abstract

Psychiatric disorders are highly heritable pathologies of altered neural circuit functioning. How genetic mutations lead to specific neural circuit abnormalities underlying behavioral disruptions, however, remains unclear. Using circuit-selective transgenic tools and a mouse model of maladaptive social behavior (ArpC3 mutant), we identify a neural circuit mechanism driving dysfunctional social behavior. We demonstrate that circuit-selective knockout (ctKO) of the ArpC3 gene within prefrontal cortical neurons that project to the basolateral amygdala elevates the excitability of the circuit neurons, leading to disruption of socially evoked neural activity and resulting in abnormal social behavior. Optogenetic activation of this circuit in wild-type mice recapitulates the social dysfunction observed in ArpC3 mutant mice. Finally, the maladaptive sociability of ctKO mice is rescued by optogenetically silencing neurons within this circuit. These results highlight a mechanism of how a gene-to-neural circuit interaction drives altered social behavior, a common phenotype of several psychiatric disorders.

Indexed as

Actin-Related Protein 2-3 ComplexAnimalsBasolateral Nuclear ComplexCytoskeletonDisease Models, AnimalMaleMental DisordersMiceNerve NetNeuronsOptogeneticsPatch-Clamp TechniquesPrefrontal CortexSocial BehaviorActin-Related Protein 2-3 ComplexArpc3 protein, mouseArp2/3ArpC3basolateral amygdalacircuit pathologycytoskeletonneural circuitprefrontal cortexschizophreniasocial behavior

Identifiers

PMID32726629
PMCPMC8000056
OpenAlexW3045924150

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.