Evidence map›Paper›PMID 21254450›Full record

ArticleAutism research : official journal of the International Society for Autism Research2011

Absence of preference for social novelty and increased grooming in integrin β3 knockout mice: initial studies and future directions.

Michelle D Carter, Charisma R Shah, Christopher L Muller, Jacqueline N Crawley, Ana M D Carneiro, Jeremy Veenstra-VanderWeele

Open access · greenAbstract read
In one paragraph

Article in Autism research : official journal of the International Society for Autism Research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

59 citing papers in PubMed, 122 citations in OpenAlex.

  1. Article
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  7. CRISPR-mediated activation of autism geneMolecular therapy. Nucleic acids · 2022
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  9. Integrins Bidirectionally Regulate the Efficacy of Inhibitory Synaptic Transmission and Control GABAergic Plasticity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  10. Review
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  13. Article
  14. Review
  15. Article
  16. The K328M substitution in the human GABANeurobiology of disease · 2021
    Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Michelle D CarterDepartment of Psychiatry, Vanderbilt University, Nashville, Tennessee 37232, USA.
Charisma R Shah
Christopher L Muller
Jacqueline N Crawley
Ana M D Carneiro
Jeremy Veenstra-VanderWeele
Vanderbilt University · USJohn F. Kennedy Center for the Performing Arts · USNational Institute of Mental Health · US

Funding

THREE-TIERED PREVENTION MODEL TO BETTER SERVE ALL STUDENP30HD015052 · NICHD · VANDERBILT UNIVERSITY · PI DYKENS, ELISABETH MAY · 1985 to 2014
$18.6M
Program in NeurogenomicsT32MH065215 · NIMH · VANDERBILT UNIVERSITY · PI ROGER J COLBRAN · 2002 to 2026
$6.4M
Animal Models Of Neuropsychiatric DisordersZIAMH002179 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI CRAWLEY, JACQUELINE N · 2009 to 2012
$6.4M
Murine Genetic Models of AutismK08MH081066 · NIMH · VANDERBILT UNIVERSITY · PI VEENSTRA-VANDERWEELE, JEREMY · 2007 to 2011
$832k
NICHD NIH HHS HD15052NICHD NIH HHS P30 HD015052NIMH NIH HHS K08 MH081066NIMH NIH HHS K08-MH081066NIMH NIH HHS T32 MH065215NIMH NIH HHS T32-MH065215
6 · The paper itself

Abstract

Elevated whole blood serotonin 5-HT, or hyperserotonemia, is a common biomarker in autism spectrum disorder (ASD). The integrin β3 receptor subunit gene (ITGB3) is a quantitative trait locus for whole blood 5-HT levels. Recent work shows that integrin β3 interacts with the serotonin transporter (SERT) in both platelets and in the midbrain. Furthermore, multiple studies have now reported gene-gene interaction between the integrin β3 and SERT genes in association with ASD. Given the lack of previous data on the impact of integrin β3 on brain or behavioral phenotypes, we sought to compare mice with decreased or absent expression of the integrin β3 receptor subunit (Itgb3 +/- and -/-) with wildtype littermate controls in behavioral tasks relevant to ASD. These mice did not show deficits in activity level in the open field or anxiety-like behavior on the elevated plus maze, two potential confounds in the evaluation of mouse social behavior. In the three-chamber social test, mice lacking integrin β3 were shown to have normal sociability but did not show a preference for social novelty. Importantly, the absence of integrin β3 did not impair olfaction or the ability to recall familiar social odors. Additionally, mice lacking integrin β3 showed increased grooming behavior in novel environments. These preliminary studies reveal altered social and repetitive behavior in these mice, which suggests that the integrin β3 subunit may be involved in brain systems relevant to ASD. Further work is needed to fully characterize these behavioral changes and the underlying brain mechanisms.

Indexed as

Disease Models, AnimalExploratory BehaviorGroomingSocial BehaviorAnimalsBrainChildChild Development Disorders, PervasiveChoice BehaviorHumansIntegrin beta3MaleMiceMice, Inbred C57BLMice, KnockoutMotor ActivityIntegrin beta3Serotonin

Identifiers

PMID21254450
PMCPMC3073711
OpenAlexW2084354583

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.